PROCESSES FOR THE PREPARATION OF R-(+)-3-(CARBAMOYL METHYL)-5-METHYLHEXANOIC ACID AND SALTS THEREOF Cross-Reference to Related Applications [001] This application claims the benefit of priority to U.S. provisional application Serial Nos.: 60/808,320, filed May 24,2006; 60/814,245, filed June 15, 2006; 60/843,817, filed September 11,2006; 60/850,868, filed October 10,2006; 60/918,177, filed March 14, 2007; and 60/920,348, filed March 26,2007, hereby incorporated by reference. Field of the Invention [002] The invention encompasses processes for the synthesis of R-(+)-3-(carbamoylmethyl)-5-methylhexanoic acid ("R-CMH") and salts thereof, intermediates in the synthesis of S-pregabalin. Background of the Invention [003] (S)-Pregabalin, (S)-(+)-3-(armnomethyl)-5-methylhexanoic acid, a compound having the chemical structure. (S)-Pregabalin is a -^amino butyric acid or (S)-3-isobutyl (GABA) analogue. (S)-Pregabalin has been found to activate GAD (L-glutamic acid decarboxylase). (S)-Pregabalin has a dose dependent protective effect on-seizure, and is a CNS-active compound. (S)-Pregabalin is useful in anticonvulsant therapy, due to its activation of GAD, promoting the production of GABA, one of the brain's major inhibitory neurotransmitters, which is released at 30 percent of the brains synapses. (S)-Pregabalin has analgesic, anticonvulsant, and anxiolytic activity. [004] Preparation of (S)-Pregabalin, as disclosed in U.S. Patent No. 5,616,793, and in DRUGS OF THE FUTURE, 24 (8), 862-870 (1999) is performed by obtaining the intermediate, 3-(carbamoylmethyl)-5-methylhexanoic acid ("CMH"), which is then optically resolved to give R-CMH, which is then converted to (S)-Pregabalin, as described in the following scheme: Scheme rimoved [005] There is a need in the art for additional processes for preparing R- CMH and salts thereof. Summary of the Invention [006] In one embodiment, the invention encompasses a process for preparing (R)-(+)-3-(carbamoyImethyl)-5-methylhexanoic acid or a salt thereof having the formula FORMULA REMOVE comprising: a) asymmetrically ring opening 3-isobutylglutaric anhydride to obtain a chiral ester having the formula FORMULA REMOVE b) amidating the chiral ester to obtain a (R)-(+)-3-(carbamoylmethyl)-5-methylhexanoic acid salt having the formula FORMULA REMOVE and, optionally, c) converting the (R)-(+)-3-(carbamoylmethyl)-5-methylhexanoic acid salt to (R)-3-(carbamoylmethyl)-5-methyIbtexanoic acid, wherein R1 and R2 are independently selected from the group consisting of H, aliphatic, branched or cyclic C1 to C12 hydrocarbyl, C6 to C9 aromatic hydrocarbyl and CO2H, and M is either H or NlV. [007] In another embodiment, the invention encompasses a process for preparing R-(+)-3-(carbamoylmethyl)-5-methylhexanoic acid or a salt thereof having the formula FORMULA REMOVE comprising: a) combining 3-isobutylglutaric anhydride, a chiral alcohol, a solvent • selected from the group consisting of C6-10 aromatic hydrocarbons, C3-5 ketones, C2-5 ethers, C2-7 esters, C1-2 halogenated hydrocarbons, and C1-4nitriles, and a base to obtain a chiral ester of the formula FORMULA REMOVE b) mixing with ammonia to obtain a (R)-+)-3-(carbamoylmethyl)-5-methylhexanoic acid salt having the formula FORMULA REMOVE ; and, optionally, c) adding an acid to obtain R-(+)-3-(carbamoylmethyl)-5-methylhexanoic acid, wherein R1 and R2 are independently selected from the group consisting of H, aliphatic, branched, or cyclic C1-12 hydrocarbons, C6-9 aromatic hydrocarbons, and CO2H; and M is either H or NH4+. [008] In another embodiment, the invention encompasses a process for preparing R-(+)-3-(carbamoylmethyl)-5-methylhexanoic acid or a salt thereof having the formula FORMULA REMOVE comprising: a) combining 3-isobutylglutaric mxhydnde, a non-chiral alcohol, a chiral amine, and a solvent selected from the group consisting of C6-10 aromatic hydrocarbons, C2-5 ethers, C1-2 halogenated hydrocarbons, and mixtures thereof to obtain a chiral ester of the formula FORMULA REMOVE b) mixing with ammonia to obtain a CRcarbamoylmethyl)-5-methylhexanoic acid salt having the formula FORMULA REMOVE ; and, optionally, c) adding an acid to obtain R(-)-3-(carbamoylmethyl)-5-methylhexanoic acid, wherein R1 and R2 are independently selected from the group consisting of H, aliphatic, branched, or cyclic C1-12 hydrocarbons, C6-9 aromatic hydrocarbons, and CO2H; and M is either H or NH4+. [009] In another embodiment, the invention encompasses a process for preparing R-(+)-3-(carbamoylmethyl)-5-m©thyJhexanoic acid or a salt thereof having the formula FORMULA REMOVEcomprising: a) combining a chiral ester having the formula FORMULA REMOVE with an acid activating agent to form an activated acid derivative having the formula FORMULA REMOVE b) amidating the activated acid derivative to obtain a carbamoyl ester having the formula c) hydrolyzing the carbamoyl ester with an acid or a base to obtain R-(+)-3-(carbamoylmethyl)-5-methylhexanoic pcid or a salt thereof, respectively; and, ptionally, d) converting the salt of R-(+)-3-(qarbamoylmethyl)-5-methylhexanoic acid into R-(+)-3-(carbamoylmethyl)-5-methylhexanoic acid, wherein R1 and R2 are independently selected from the group consisting of H, aliphatic, branched, or cyclic C1-12 hydrocarbons, C6-9 aromatic hydroccfbons, and CO2H; and LG is a leaving group; where the leaving group is derived from the acid activating agent; and wherein X is H or an alkali metal. [0010] In another embodiment, the invention encompasses a process for preparing (S)-pregabalin comprising preparing R-(+)-3-(carbamoylmethyl)-5-methylhexanoic acid or salts thereof by any of the above-described processes, and converting the R-(+)-3-(carbamoylmethyl)-5-methylhexanoic acid or salts thereof into (S)-pregabalin. Detailed Description of the Invention [0011] The invention encompasses processes for the preparation of R-CMH, in high yields, without resolving the CMH raccjnate, as disclosed in the prior art and therefore, avoiding the resolution and the recovery of the undesired enantiomer. In addition, the processes can be adapted easily to an industrial scale. [0012] In one embodiment, the invention encompasses a process for preparing R-CMH or a salt thereof that may be illustrated by the following Scheme 1. Scheme 1. Process for Preparing R-CMH or a Salt Thereof from 3-Isobutylghrtaric Anhydride wherein R1 and R2 are independently selected from the group consisting of H, aliphatic, branched, or cyclic C1-12 hydrocarbons, C6-9 aromatic hydrocarbons, and CO2H; and M is either H or NH4. Preferably, R1 is C02H or H; R2 is H, a C6-9 aromatic hydrocarbon, or an aliphatic or branched C1-12 hydrocarbon; or Ri and R2 form together a cyclic CHI hydrocarbon. [0013] Preferably, the d-9 aromatic hydrocarbon is phenyl. Preferably, the aliphatic or branched C1-12 hydrocarbon is methyl. Preferably, the cyclic C1-12 hydrocarbon is l,3,3-trimethylbicyclo[2.2.1]heptane. Preferred combinations of R, and R2 are CO2H and phenyl, H and H, H and Me, H and phenyl, respectively, or R1 and R2 form together l,3,3-trimethylbicyclo[2.2.1]heptane of the following formula FORMULA REMOVE [0014] The asymmetric ring opening step may be accomplished with either (i) a chiral alcohol, or (ii) with a non-chiral alcohol in combination with a chiral amine, which acts as a chiral inductor. [0015] When a chiral alcohol is used, the asymmetric ring opening step typically comprises combining 3-isobutylglutsric anhydride ("IBG-anhydride"), a chiral alcohol S-ester, a solvent selected from the group consisting of C6-10 aromatic hydrocarbons, C3-5 ketones, C2-5 ethers, C2-7 esters, C1-2 halogenated hydrocarbons, and C1.4 nitriles, and a base. [0016] Preferably, the base is selected from the group consisting of sodium hydride ("NaH") and butyl lithium (Buli"). More preferably, the base is the inorganic base NaH. Preferably, the NaH is in the form of a 60% w/w suspension in oil [0017] The chiral alcohol opens IBG-aahydride in a stereospecific manner. Thus, one of ordinary skill in the art would appreciate that one enantiomer of the chiral alcohol leads to the formation of the S-ester, while the opposite enantiomer leads to the fonnation of the R-ester. Examples of suitable chiral alcohols include, but not limited to, (S)-fenchyl alcohol, (S)-mandelic acid, benzylmandelate, ethylmandelate, methylmandelate, 1-phenylethanol, l-phenyl-2-propanol, 1-phenyl-l-propanol, and trifluoromethyl-benzyl alcohol. Preferably, the chiral alcohol is either (S)-fenchyl alcohol or (S)- mandelic acid. [0018] Preferably, the C6-10 aromatic hydrocarbon is a C6-8aromatic hydrocarbon, more preferably a Q6-7 aromatic hydrocarbon, and most preferably toluene. Preferably, the C3.5 ketone is a C3-4ketone, more preferably a C3 ketone, and most preferably acetone. A preferred C2-5 ether is a C4-5 ether, and a more preferred C2-5ether is either tetrahydrofuran ("THF"), or methyl tert-butylether ("MTBE"). Preferably, the C2-7 ester is a C2-5 ester, more preferably a C2-4 ester, and most preferably a C4 ester. A particularly preferred C2-7 ester is ethyl acetate. A preferred C1.2 halogenated hydrocarbon is a C1 halogenated hydrocarbon, and a more preferred Cj-2 halogenated hydrocarbon is dichloromefhase ("DCM"). Preferably, the C1-4 nitrile is a C1-2 nitrile, more preferably a C2 nitrile, and most preferably acetonitrile ("ACN"). The most preferred solvent is toluene. [0019] Typically, the solvent and the chiral alcohol are combined first to provide a mixture, and the base is then added to the mixture. Preferably, the inorganic base is added to the mixture at a temperature of about -78°C to about 110*C, more preferably about -40°C to about 40°C, and most preferably at about -20°C to about 20°C. [0020] After the addition of the base, IBG-arjhydride is added to the mixture. The IBG-anhydride can be provided neat or in the form of a solution. When provided in the form of a solution, the solvent is as described above. The IBG-anhydride may be added drop-wise. When the anhydride is added drop-wise, the addition is preferably done over a period of about 0.5 hour to about 3 hours, more preferably about 0.5 hour to about 1 hour. [0021 ] After the addition of the IBG-anhydride, the mixture is preferably maintained at a temperature of about 0°C to about 50°C, and more preferably about 20°C to about 30°C, to obtain the S-ester having the following structure. Structure Rimoved Preferably, the mixture is maintained for about 1 to about 6 hours, and more preferably for about 3 hours. [0022] When a non-chiral alcohol m combination with a chiral amine is used, the asymmetric ring opening step typically comprises combining IBG-anhydride, a chiral amine, a non-chiral alcohol, and a solvent selected from the group consisting of C6-10 aromatic hydrocarbons, C2-5 ethers, C1-2 halogenated hydrocarbons, and mixtures thereof. [0023] Preferably, the C6-10 aromatic hydrocarbon is a C6-8 aromatic hydrocarbon, more preferably a C6-7 aromatic hydrocarbon, and most preferably toluene. A preferred C2-5 ether is a C4-5 ether and a more preferred C2-5 ether is THF. A preferred C1-2 halogenated hydrocarbon is a C1 halogenated hydrocarbon and a more preferred C1-2 halogenated hydrocarbon is DCM. The most preferred solvent is toluene. [0024] The chiral amine serves as a chiral inductor for the non-chiral alcohol, thereby leading to a stereospecific opening of IBG-anhydride. Thus, one of ordinary skill in the art would appreciate that one enantiomer of the chiral amine leads to the formation of the S-ester, while the opposite ensntiomer leads to the formation of the R-ester. Preferably, the chiral amine is a chiral alkaloid. Preferably, the chiral alkaloid is a cinchona alkaloid. Examples of suitable cinchona alkaloids include, but are not limited to, quinidine, cinchonine and their dehydro derivatives. Preferably, the chiral amine is quinidine of the following structure: Quiatttfise [0025] Preferably, the non-chiral alcohol is a C1.7 alcohol. Preferably, the C1.7 alcohol is methanol, ethanol, propanol, n-butanol, and benzyl alcohol. More preferably, the C1-7 alcohol is methanol. [0026] Typically, the non-chiral alcohol is added to a suspension of the IBG- anhydride and the chiral amine in a solvent selected from the group consisting of C6-10 aromatic hydrocarbons, C2-5 ethers, C1-2 halogcnated hydrocarbons, and mixtures thereof. Preferably, the alcohol is added to the suspension at a temperature of about 20°C to about -78°C, more preferably about -40*C to about -60°C. The non-chiral alcohol may be added drop-wise to the suspension. When the addition is drop-wise, it is preferably done over a period of about 15 minutes to about 45 minutes. [0027] Typically, the addition of the non-chiral alcohol to the suspension provides a mixture. Preferably, the mixture is stirred for about 2 to about 96 hours and more preferably for about 2 to about 24 hours, to obtain the S-ester of the following formula. FORMULA REMOVE [0028] The above S-ester prepared by either of the above methods may be recovered by any method known to one of ordinary skill in the art. Such methods include, but are not limited to, removing the solvent, and optionally adding an acid, and drying. [0029] Typically, the recovered S-estcr is a mixture of two diastereomers, referred to as S-ester and R-ester of the following formulas: FORMULA REMOVE where the S-ester is the major diastereomer in the mixture. Preferably, the diastereomeric ratio is about 80:20 to about 95:5 area by HPLC, of the S-ester to the R-ester, respectively. [0030] Optionally, the recovered mixture of diastereomers can be crystallized to increase the ratio of the S-ester to the R-ester, prior to reacting with ammonia. The crystallization comprises dissolving the mixture of diastereomers in a solvent selected from the group consisting of C6-10 aromatic hydrocarbons, C3-5 ketones, C2-5 ethers, C2-7 esters, C1-2 halogenated hydrocarbons, C1-4 nitriles, and mixtures thereof, and precipitating the S-ester from the solution, while the R-ester remains in solution. Preferably, the mixture of diastereomers is dissolved in a mixture of solvents. A preferred mixture of solvents is that of a C6-10 aromatic hydrocarbon and a C2.7 ester. More preferably, the mixture is that of toluene and ethyl acetate. [0031] The mixture of diastereomers and solvent may optionally be heated to dissolve the mixture of diastereomers to form a solution. Preferably, the combination is heated to a temperature of about 40°C to about 150"C, and more preferably about 60°C to about 120°C. Typically, the obtained solution is cooled to precipitate the S-ester. Preferably, the solution is cooled to a ternperature of about 30°C to about 0°C, and more preferably about 20°C to about 2CC. The precipitated S-ester may be recovered by filtration. [0032] Typically, the crystallized S-ester contains less of the R-ester than the starring S-ester. Preferably, the ratio of the two diastereomers is of at least 95:5 area by HPLC of the S-ester to the R-ester, respectively. [0033] The amidation step comprises mixing the S-ester of the chiral ester, obtained by any of the above processes, with emmonia, and optionally, followed by adding an acid. The reaction between the S-ester and ammonia leads to the R-CMH ammonium salt of the formula ,FORMULA REMOVE [0034] Preferably, the ammonia is provided in the form of a solution in a solvent selected from the group consisting of water, an organic solvent, and mixtures of water and organic solvent. Preferably, the organic solvent is selected from the group consisting of: methanol, ethanol, ethylene glycol, isopropanol, ethylacetate, and acetonitrile. The solution of ammonia can be obtained by bubbling ammonia gas into the solvent. NHUC1 may also be combined with the ammonia and the S-ester. [0035] Preferably, the combination of the S-ester and ammonia forms a mixture, which is maintained at a temperature Of about -40°C to about 110°C, more preferably, at about 40°C to about 110°C, and most preferably at about 40°C to about 80°C to obtain the ammonium salt of R-CMH. Preferably, the mixture is maintained for about 2 to about 48 hours, and more preferably for about 6 to 30 hours. Preferably, the mixture is maintained at a pressure of about 1 to about 6 atmospheres, and more preferably about 1 to about 5 atmospheres. [0036] Preferably, the acid is selected ftom the group consisting of HC1, HBr, H2SO4, H3PO4, acetic acid, and formic acid. More preferably, the acid is HC1. [0037] Preferably, the acid is present in an amount sufficient to obtain a pH of about 0 to about S, and more preferably about 2 to about 4. After the acid is added, cooling is conducted to precipitate the R-CMH. Preferably, the cooling is to a temperature of about 10°C to about -5°C, and more preferably to about 5°C to about 0"C. [0038] The R-CMH or its salt thus obtained may be recovered by any method known to one of ordinary skill in the art Such methods include, but are not limited to, filtering, extracting the R-CMH or its salt with a solvent, evaporating the solvent and drying. [0039] Preferably, the asymmetric ring opening and the amidation can be performed as one-pot processes, i.e., without isolation of the S-ester. [0040] In another embodiment, the invention encompasses a process for preparing R-CMH and salts thereof that may be illustrated by the following Scheme 2. Scheme 2. Process for Preparing R-CMH or Salts Thereof from an R-Ester Scheme removed wherein R1 and R2 are independently selected from the group consisting of H, aliphatic, branched, or cyclic C1-12 hydrocarbons, C6-9 aromatic hydrocarbons, and CO2H; LG is a leaving group, where the leaving group is derived from the acid activating agent; and X is either H or an alkali metal. Preferably, R=1 is CO2H or H; R2 is H, a C6-9 aromatic hydrocarbon, or an aliphatic or branched C1-12 hydrocarbon; or R1 and R2 form together a cyclic C1-12 hydrocarbon. [0041] Preferably, the C6-9 aromatic hydrocarbon is phenyl. Preferably, the aliphatic, or branched C1-12 hydrocarbons is methyl. Preferably, the cyclic C1-12 hydrocarbon is l,3,3-trimeftylbicyclo[2.2.1Jhcpiane. Preferred combinations of R1 and R2 are CO2H and phenyl, H and H, H and Me, H and phenyl, respectively, or R1 and R2 form together l,3,3-trimethylbicyclo[2.2,l]heptane of the formula FORMULA REMOVE [0042] chiral.The ester moiety in the acid starting material can be chiral or non- [0043] The starting R-ester can be provided by the above process using the chiral alcohol or the combination of the non-chiral alcohol and the chiral amine with the proviso that the opposite enantiomer of the chiral alcohol and of the chiral amine is used. The opposite enantiomer leads to the formation of the R-ester, rather than the S-ester as above. £0044] Examples of suitable chiral alcohols include, but are not limited to, (R)-fenchyl alcohol, (R)-mandelic acid, and the opposite enantiomer of the following alcohols: benzylmandelate, ethyhnandelate, mcthylmandelate, l-phenylethanol, 1-phenyl-2-propanol, 1-phenyl-l-propanol, and trifluoromethyl-benzyl alcohol. Preferably, the chiral alcohol is either (R)-fenohyl alcohol or (R)-mandelic acid. [0045] Preferably, the chiral amine is a chiral alkaloid. Preferably, the chiral alkaloid is a cinchona alkaloid. Examples for suitable cinchona alkaloids include, but not limited to, quinine, cinchonidine and their dehydro derivatives. Preferably, the chiral amine is quinine of the following structure: structure Rimoved [0046] The activation of the R-ester may be accomplished by combining the above R-ester, a base, and an acid activating agent in a solvent selected from a group consisting of C6-10 aromatic hydrocarbons, C3-5 ketones, C2-5 ethers, C2-7 esters, C1-2 halogenated hydrocarbons, C1-4 nitriles, and mixtures thereof to obtain an activated acid derivative of the formula FORMULA REMOVE [0047] The base can be ah organic base or an inorganic base. Preferably, the organic base is an aliphatic amine, and more preferably a C2-12 aliphatic amine. Preferably, the C2-12 aliphatic amine is selected from the group consisting of ethyl amine, diethyl amine, propyl amine dipropyl amine, butyl amine, tributylamine, diisopropyl amine, and triethylamine. Most preferably, the C2-12 aliphatic amine is triethylamine. [0048] Preferably, the inorganic base is an alkaline hydroxide, an alkaline carbonate or an alkaline bicarbonate. Preferably, the alkaline hydroxide is sodium hydroxide or potassium hydroxide. Preferably, the alkaline carbonate is either sodium carbonate or potassium carbonate. Preferably, the alkaline bicarbonate is either sodium bicarbonate or potassium bicarbonate. More preferably, the base is triethylamine. [0049] Preferably, the C6-10 aromatic hydrocarbon is a C6-8 aromatic hydrocarbon, more preferably a C6-7 aromatic hydrocarbon, and most preferably toluene. Preferably, the C3-5 ketone is a C3-4 ketone, more preferably a C3 ketone, and most preferably acetone. A preferred C2-5 ether is a C4-5 ether and a more preferred C2-5 ether is THF or MTBE. Preferably, the C2-7 ester is a C2-5 ester, more preferably a C2-4 ester, and most preferably a G4 ester. A particularly preferred C2-7 ester is ethyl acetate. A preferred C1-2 halogenated hydrocarbon is a C1 halogcnated hydrocarbon and a more preferred C1-2 halogenated hydrocarbon is DCM. Preferably, the CM nitrile is a C1-2 nitrile, more preferably a C2 nitrile, and most preferably ACN. The most preferred solvent is DCM. [0050] The term "acid activating agent" refers to a substance containing a group that activates a carbonyl group, i.e., makes the carbonyl group more susceptible to nucleophilic attack, when attached to it. Preferably, the acid activating agent is selected from a group consisting of: alkyl halo formates, anhydrides, and sulfonyl halides. Preferably, the alkyl halo formate is ethyl chloroformate or methyl chloroformate. Preferably, the anhydride is a symmetric or mixed anhydride, more preferably, acetic anhydride. Preferably, the sulfonyl halide is mesyl chloride or tosyl chloride. More preferably, the activating agent is ethyl chloroformate [0051 ] Typically, the solvent is combined with the starting R-ester and the base to obtain a mixture. The mixture is then cooled prior to the addition of the acid activating agent. Preferably, the mixture is cooled to a temperature of about 20°C to about -5°C, and more preferably to about 5°C to about 0°C. [0052] After the acid activating agent is added to the mixture, the mixture is wanned. Preferably, the mixture is warmed to a temperature of about 10°C to about 50°C, and more preferably, to about 20°C to about 25°C. Preferably, the wanned mixture is maintained for about 1 to about 2 hours to obtain the activated acid derivative of the following formula : FORMULA REMOVE [0053] Preferably, R1 and R2 are H, and LG is OCChEt, providing an activated acid derivative of the following formula: The activated acid derivative is then subjected to an amidation processthat comprises combining the above activated acid derivative with ammonia, followed by addition of an acid or a base to obtain R-CMH. The reaction of the activated acid derivative with ammonia provides a slurry having the following amide. [0055] The ammonia can be provided as described above. Preferably, the ammonia is provided in the form of a gas. [0056] The amide may be recovered froto the slurry by any method known to one of ordinary skill in the art. Such memods include, but are not limited to, filtering the amide from the slurry, washing the amide, and drying the amide. Alternatively, the amide can be reacted with the acid or base without being isolated, i.e., in a one-pot reaction. [0057] The ester group of the above amide is then hydrolyzed to R-CMH or a salt thereof by combining the amide with an acid or a base. When an acid is used, the above amide is hydrolyzed to R-CMH. When a base is used, the above amide is hydrolyzed to a salt of R-CMH. The salt of R-CMH can then be converted into R-CMH by adding an acid. [0058] The acid can be an inorganic acid or an organic acid. Preferably, die inorganic acid is selected from the group consisting of HC1, HBr, H2SO4, and H3PO4, and more preferably HC1. Preferably, the organic acid is selected from the group consisting of acetic acid and formic acid. Most preferably, the acid is HC1. [0059] The base is an inorganic base. Preferably, the base is an alkali metal base, thereby forming an alkali metal salt of R-CMH during the hydrolysis. Preferably the inorganic base is selected from the group consisting of NaOH, KOH and IiOH, and most preferably NaOH. [0060] Preferably, the amide is combined with the acid or base to provide a mixture, which is stirred at a temperature of about 10°C to about 50°C, and more preferably at about 20°C to about 25"C. Preferably, the mixture is stirred for about 1 to about 10 hours, and more preferably for about 2 to about 8 hours, to obtain the R-CMH or salt thereof. [0061] The R-CMH or salt thereof thus obtained may be recovered by any method known to one of ordinary skill in ths sit. Preferably, the R-CMH or salt thereof is recovered by adjusting the pH of the stirred mixture to about 1 to about 6, more preferably to about 2 to about 5, to provide a slurry; filtering the R-CMH or salt thereof from the slurry; washing the filtered R-CMH or salt thereof; and drying the R-CMH or salt thereof. Preferably, the pH is adjusted by adding a base to the mixture. Preferably, the base is an inorganic base and more preferably the base is selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate. Optionally, an organic base, such as ammonia, can be used. Typically, the inorganic base can be used as a solid or as an aqueous solution. [0062] The R-CMH or salt thereof prepared by any of the above-described processes may be converted to (S)-pregabaiin. The conversion may be performed, for example, according to the processes disclosed in U.S. Patent application No. 2007/0073085, hereby incorporated by reference. Examples Asymmetric ring opening of ffiG-anhydride Example 1: Preparation of Fenchvl ester [0063] A three-neck-flask (0.25 1) was eharged with toluene (140 ml), Fenchyl alcohol (9.26 g) and NaH-60% (2.4 g). The mixture was heated to 80°C, and then cooled to 5°C. A solution of 3-isobutyl glutaric anhydride (6.8 g) in toluene (25 ml) was added to the mixture dropwise. The solution was stirred for 3 hours at room temperature. The solvent was evaporated to dryness to obtain the crude ester. The solid was dried at 55°C under vacuum Example 2: Isolation of (SI. (RV Fenchvl ester [0064] The crude ester prepared in example 1, is added to a mixture of ethyl acetate and toluene, and heated to 80°C (range 40° to 100°C) until dissolution. The solution is cooled to 2°C (range 0° to 20°C) to get a yellowish solid of (S)-3-(l,3,3-trimethylbicyclo[2.2.1]heptan-2-yl)carbonyi)methyl>5-methylhexanoic acid (Fenchyl ester), which is filtered from the mixture. Example 3: Preparation and isolation of (S). fltymandelatc ester [0065] A three-neck-flask (0.25L) is charged with toluene (70 ml), S-mandelic acid (3.04 g) and NaH-60% (1.6 g). The mixture is heated to reflux and then cooled to room temperature. 3-isobutyl glutaric anhydride (3.4 g) is added drop-wise. [0066] The solution is stirred for 6 hours at room temperature. The solvent is evaporated, and the residue is crystallized from ethyl acetate and toluene mixture to get an off-white solid of (S)-4-(((S)-carboxy(phGayl)methoxy)carbonyl)-3- isobutylbutanoic acid (Mandelate ester). [0067] The solid is dried at 55°C under vacuum. Example 4: Asymmetric ring opening of IBG-anhvdride with chiral alkaloide [0068] A three-neck-flask (0.25L) is charged with quinidine (11 mmol), 3- isobutyl glutaric anhydride (10 mmol) and toluene (50 ml). The mixture is cooled at -55°C. Methanol (30 mmol) is added dropwise over a period of 10 min to the cooled suspension. The reaction is stirred at for 96 h. The solution is concentrated to dryness, and the resulting residue is dissolved in diethyl ether (65 ml). The solution is washed with HC1-2N, and the aqueous layer is back-extracted with ether. The combined organic layers are dried with MgSQt, and filtered. The filtrate is evaporated to dryness. Example 5: Asymmetric ring opening of IBG-anhvdride with chiral alkaloide [0069] Methanol (6.2ml, 153mmol) was added to a flame-dried 250ml single, round-bottomed flask equipped with magnetic stirrer and charged with Quinidine (7.14g, 22mmol), 3-isobutyl glutaric anhydride (3.28g, 19.3mmol) and Toluene (100ml, 30.5vol) at -75°C. The reaction was stirred for 21 hours. The solution was concentrated to dryness, and the resulting residue was dissolved in diethyl ether (125 ml). The solution was washed with HC1-2N (40ml x 3), and the aqueous layer was back-extracted with ether. The combined organic layers were evaporated until dryness, to give 3.56g of a yellow oil of S-hcmiester ( (S)-3-((methoxycarbonyl)methyl)-5-methylhexanoic acid) (Optical purity 90%, Yield -91%). Example 6: Asymmetric ring opening of IBG-anhydride with chiral alkaloide [0070] Methanol (6.2ml, 153mmol) was added to a 250ml three-necked, round-bottomed flask equipped with magnetic stirrer and charged with Quinidine (7.14g, 22mmol), 3-isobutyl glutaric anhydride (3.28g, 19.3mmol) and Toluene (100ml, 30.5vol) at -50°C. The reaction was stirred for 2 hours. The slurry was washed with H2SO4-2N (40ml x 3). The organic layer was evaporated until dryness, to have 3.7g yellow oil of S -Hemiester (Optical purity 90% Yield - 95%). Example 7: Asymmetric ring opening of IBG-anhydride with chiral alkaloide [0071] Methanol (6.2ml, 153mmol) was added to a 250ml three-necked, round-bottomed flask equipped with magnetic stirrer and charged with Quinidine (12.5g, 38.6mmol), 3-isobutyl glutaric anhydride (3.28g, 19.3mmol) and Toluene (100ml, 30.5vol) at -78°C. The reaction was stirred for 22.5 hours. The slurry was washed with HC1-2N (40ml x 3). The organic layer was evaporated until dryness, to have 3.63g yellow oil of S-Hemiester (Optical purity 90%, Yield - 93%). Example 8: Asymmetric ring opening of IBG-anhvdride with chiral alkaloide [0072] Methanol (6.2ml, 153mmol) was added to a 250ml three necked, round-bottomed flask equipped with magnetic Stirrer and charged with Quinidine (7.14g, 22mmol), 3-isobutyl glutaric anhydride (3.28g, 19.3mmol) and Toluene (33ml, lOvol) at -78°C. The reaction was stirred for 19 hours. The solution was washed with HC1-2N (25ml x 3). The organic layer was evaporated until dryness, to give 3.38g yellow oil of S-Hemiester (Optical purity 90%, Yield - 87%). Example 9: Asymmetric ring opening of ffiG-anhvdride with chiral alkaloide [0073] Methanol (6.2ml, 153mmoJ) was added to a 250ml three-necked, round-bottomed flask equipped with magnetic stirrer and charged with Quinidine (7.14g, 22mmol), 3-isobutyl glutaric anhydride (3.28g, 19.3mmol) and Toluene (100ml, 30vol) at ~78°C. The reaction was stirred for 2 hours. The slurry was washed with H2SO4-2N (40ml x 3). The organic layer was evaporated until dryness, to give 3.4g yellow oil of S-Hemiester (Optical purity 95%, Yield - 93%). Example 10: Asymmetric ring opening of JBQ-anhvdride with chiral alkaloide [0074] To a stirred suspension of 3-isobutyl glutaric anhydride (88 mmol) and Quinidine (100 mmol) in Toluene (30vol) at -50°C, Methanol (273 mmol) was added drop-wise. The reaction was stirred at -50°C for 17 h. The solution was washed with H2SO4-2N. The organic layer was evaporated to dryness to obtain S-Hemiester. (Optical purity - 94%, Yield - 94%). Example 11; Asymmetric ring opening of IBCr-anhydride with chiral alkaloide [0075] To a stirred suspension of 3-isobutyl glutaric anhydride (19.3 mmol) and Quinidine (22 mmol) in Toluene (20vol) at -50*C, Methanol (59.8 mmol) was added drop-wise. The reaction was stirred at -50°C for 17 hours. The solution was washed with H2SO4-2N. The organic layer was evaporated to dryness to obtain S-Hemiester. (Optical purity - 95%, Yield - 89%). Example 12: Asymmetric ring opening of IBG-anhvdride with chiral alkaloide [0076] To a stirred suspension of 3-isobutyl glutaric anhydride (19.3 mmol) and Quinidine (22 mmol) in Toluene (lOvol) at -50°C, Methanol (59.8 mmol) was added drop-wise. The reaction was stirred et -50°C for 4 hours. The solution was washed with H2SO4-2N. The organic layer was evaporated to dryness to obtain S-Hemiester. (Optical purity - 94%, Yield - 92%). Example 13: Asymmetric ring opening of ipG-anhvdride with chiral alkaloide [0077] To a stirred suspension of 3-isobutyl glutaric anhydride (19.3 mmol) and Quinidine (22 mmol) in Toluene (30vol) at -50°C, Methanol (193 mmol) was added drop-wise. The reaction was stirred at -S0°C for 16 hours. The solution was washed with H2SO4-2N. The organic layer was evaporated to dryness to obtain S-Hemiester. (Optical purity - 95%, Yield - 83%). Example 14: Asymmetric ring opening of IBG-anhydride with chiral alkaloide [0078] To a stirred suspension of 3-isobutyl glutaric anhydride (19.3 mmol) and Quinidine (22 mmol) in Toluene (10vol) at -50°C, Methanol (59.8 mmol) was added drop-wise. The reaction was stirred at -S0°C for 22 hours. The solution was washed with H2SO4-2N. The organic layer was evaporated to dryness to obtain S-Hemiester. (Optical purity - 91%, Yield - 92%), Example 15: Asymmetric ring opening of IBG-anhvdride with chiral alkaloide [0079] To a stirred suspension of 3-isobUtyl glutaric anhydride (270 mmol) and Quinidine (308 mmol) in Toluene (lOvol) at -50°C, Methanol (837 mmol) was added drop-wise. The reaction was stirred at -50°C for 3 hours. The solution was washed with H2SO4-2N. The organic layer was evaporated to dryness obtain S-Hemiester. (Optical purity - 95%, Yield - 84%). Example 16: Asymmetric ring opening of IBG-anhvdride with chiral alkaloide [0080] To a stirred suspension of 3-isobutyl glutaric anhydride (19.3 mmol) and Cinchonine (22 mmol) in Toluene (30vol) at -50°C, Methanol (59.8 mmol) was added drop-wise. The reaction was stirred tX -50°C for 15 hours. The solution was washed with H2SO4-2N. The organic layer was evaporated to dryness obtain S-Hemiester. (Optical purity - 78%, Yield - 99%). Example 17: Asymmetric ring opening of IBG-anhydride with chiral alkaloide [0081] To a stirred suspension of 3-isobutyl glutaric anhydride (19.3 mmol) and Cinchonidine (22 mmol) in Toluene (30vol) ot -50°C, Methanol (59.8 mmol) was added drop-wise. The reaction was stirred at -50*C for 15 hours. The solution was washed with H2SO=-2N. The organic layer was evaporated to dryness obtain R-Hemiester. (Optical purity - 68%, Yield - 100%). Example 18: Asymmetric ring opening of mG-anhvdride with chiral alkaloide [0082] To a stirred suspension of 3-isobutyl glutaric anhydride (19.3 mmol) and Cinchonine (22 mmol) in Toluene (30vol) at -78°C, Methanol (59.8 mmol) was added drop-wise. The reaction was stirred at -50°C for 19 hours. The solution was washed with H2SO4-2N. The organic layer was evaporated to dryness obtain S-Hemiester. (Optical purity - 74%, Yield - 90%). Example 19: Asymmetric ring opening of IBG-anhvdride with chiral alkaloide [0083] Methanol (6.2ml, 153mmol) wcs added drop-wise to a 250ml three- necked, round-bottomed flask equipped with magnetic stirrer and charged with Quinine (7.14g, 22mmol), 3-isobutyl glutaric anhydride (3.28g, 19.3mmol) and Toluene (100ml, 30vol) at -70°C. The reaction was stirred for 17 hours. The solution was concentrated to dryness, and the resulting residue was dissolved in diethyl ether (125 ml). The solution was washed with HC1-2N (40ml x 3). The organic layer was evaporated until dryness, to have 3.7g yellow oil of R-Hemiester (Optical purity 80%, Yield - 95%). Amidation Example 20: [0084] A three-neck-flask (0.25 1) is charged with aqueous NH3 (40 ml) and the S-Me hemiester (4 g). The mixture is heated to 80°C under pressure (5 Arm) for 6 hours. The solution is cooled to room temperatere, and HCl is added to obtain a pH of 1. The mixture is cooled to 0°C, R-CMH is filtered and dried at 55°C under vacuum. Example 21: [0085] A 50ml three-neck-flask was charged with aqueous NH3 22% (25ml, 8vol.) and S-CMH-methyl ester (MS-1750,3.16g). The solution was stirred at room temperature for 92 hours. 37% of HCl was added to obtain a pH of 3. The white slurry was cooled to 0°C, R-CMH was filtered and dried at 55°C under vacuum during 14 hours to obtain 3.65g of white powder R-CMH. (Optical purity - 90%, Yield - 100%). Example 22: [0086] An autoclave was charged with aqueous NH3 22% (25ml, 12.5vol.) and S-CMH-methyl ester (MS-1848,2g). The solution was stirred at 75°C at 2Atm for 7 hours. 37% of HC1 was added to obtain s pH of 3. Ethyl acetate (200ml) was added to the white slurry, and the precipitant remained in the aqueous phase. Water (20ml) was added to obtain clear solutions (two phases). The two phases were separated after stirred vigorously for 10 minutes. The orgamc phase was evaporated until dryness to givel.62g of R-CMH. (Optical purity 80%, Yield - 80%). Example 23: [0087] A 100ml three-neck-fiask was charged with aqueous NH3 22% (25ml, 12.5vol.) and S-CMH-methyl ester (GE-11426,2g). The solution was stirred at 40°C for 25 hours. 37% of HC1 was added to obtain a pH « 3. The white slurry was vacuum filtered and the filter cake washed with water (5ml). The white precipitate was dried at 55°C under vacuum for 17 hours to obtain 2.45g of white powder R-CMH. (Optical purity - 87%, Yield - 100%). Example 24: [0088] An autoclave (0.1L) was charged with aqueous NH3 (25ml) and S- Methyl-ester (2g). The mixture was heated to 70°C underpressure (1.5bar) for 8 hours. The solution was cooled to room temperature, and 37% HC1 was added to obtain pH 3. NH4Cl (1.8g) was added to induce precipitation of the R-CMH. The precipitated R-CMH was filtered and dried at 55°C under vacuum. (Optical purity -84%, Yield-60%). Example 25: [0089] An autoclave (0.1L) was charged with aqueous NH3 (60ml) and S- Methyl-ester (lOg). The mixture was heated to 70°C under pressure (1.5bar) for 25 hours. The solution was cooled to room temperature, and 37% HC1 was added to obtain pH 3. NH4C1 (1.8g) was added was added to induce precipitation of the R-CMH. The precipitated R-CMH was filtered and dried at 55°C under vacuum. (Yield -100%). Example 26: [0090] A solution of S-methyl-ester (20 mmol, GE-1381) in toluene (lOvol) was extracted with NH4OH 30% (2.6vol x 2) and stirred at room temperature as clear solution for 16 hours. NH4OH 30% (5.2vol) was added to the solution and stirred at room temperature for 72 hours. The solution was acidified to pH 3 with H2SO4 75%, and evaporated until dryness. The residue was triturating in acetone (20vol), the solids were filtered off, and the acetone evaporated until dryness. The resulting residue was slurried in water (20vol) for 17 hours. The precipitate was vacuum filtered and dried in a vacuum oven at 55°C for 20 hours. Example 27: [0091] A one-neck-flask (0.1 L) was charged with aqueous NH3 (18 ml), the S-ester (3 g) and ammonium chloride (0.8g» lcq). The solution was heated to 40°C and stirred at this temperature for 24 hours and at room temperature for 18.5 hours. The solution was evaporated until dryness. Distilled water (15vol.) was added and HCl was added to obtain pH of 4. The mixture was stirred for over night; R-CMH was filtered and dried at 55°C under vacuum. Example 28: One pot synthesis of R-CMH [0092] To a stirred suspension of 3-isobutyl glutaric anhydride (118 mmol) and Quinidine (134 mmol) in Toluene (10vol) at -50°C, Methanol (365 mmol) was added drop-wise. The reaction was stiired at -50°C for 17 hours. The solution was washed with H2SO4-2N. The organic layer was filtered and extracted to NH4OH (a,.) 25% (10vol).The aqueous solution was stirred in a closed flask at 40°C for 24 hours and at room temperature for 48 hours. 37% HCl was added to obtain pH 3. The slurry was stirred 20 hours at room temperature and cooled to 5*C. R-CMH was filtered and dried at 55°C under vacuum. Example 29: Preparation of fSVmethvl 3-fcarbamovlmethvlV5-methvlhexanoate [0093] A round-bottomed flask is equipped with magnetic stirrer and charged with methylene dichloride (100 ml), (S)-3-((Methoxycarbonyl)methyl)-5-methylhexanoic acid (20 g) and with triethylamme (0.77g) and cooled to 0-5°C followed by addition of ethyl chloroformato (9 g). The mixture was stirred for 1-2 h at a temperature of 20°C to 25°C, followed by quenching with 25% aqueous ammonia (100 ml). The resulted slurry is filtered and washed with water and dried to obtain a solid of (R)-methyl 3-(carbamoylmethyl)-5-methylhexanoate. Example 30: Preparation of rRV(H-V3-(carbamovlmethvl')-5-m,ethvlhexanoic acid fR-CMH1 [0094] A flask is equipped with a magnetic stirrer and is charged with 3N HC1 (100 ml) and (R)-methyl 3-(carbamoylmefiiyl-5-methylhexanoate (20 g). The mixture is stirred for 1-10 hours at a temperature of 20°C to 25 °C, followed by quenching with 47% NaOH to pH 3. The resulting slurry is filtered, washed with water, and dried to obtain a white solid of (R)-3-(carbamoylmethyl)-5-methylhexanoic acid. Example 31: Conversion of (&1-CMH to (SVFregabalin:' Example 12 from U.S. Publication No. 2007/0073085 [0095] A reactor (0.5 L) was loaded with water (165 ml) and NaOH (35.5 g) to obtain a solution. The solution was cooled to 15°C and (R)—CMH (33 g) was added. Br2 (28.51 g) was added dropwise (15 min) while keeping the temperature below 25°C. The mixture was heated to 60°C for 15 min and then cooled to 15°C. Iso-butanol was added (100 ml) and then a solution of H2S04 (66%) (33 ml) was added. The phases were separated, and the aqueous phase was extracted with Iso-butanol (83 ml). To the combined organic phases BU3N (34.2 g) was added and the mixture was cooled to 2°C, and stirred for 2 hours. The solid was filtered, washed and dried at 55°C under vacuum, providing (S)-PREGABALIN with total purity 99.86% areabyHPLC. Example 32: Conversion of (RVCMH Sodium Salt to fSVPreeabalin [0096] A reactor is loaded with water and NaOH to obtain a solution. The solution is cooled to about 15°C and (R)-CMH sodium salt is added. Br2 is added dropwise to the reactor over a period of about 15 minutes, while keeping the temperature below about 25°C. The resulting mixture is heated to about 60°C for about 15 min and then cooled to about 15°C. Iso-butanol is added and then a solution of H2SO4 (66%) is added to form a two-phase mixture. The two phases are separated, and the aqueous phase is extracted with iso-butanol. To the combined organic phases is added BU3N and the mixture is cooled to about 2°C, and stirred for about 2 hours. The resulting solid is filtered, washed and dried at 55°C under vacuum to provide (S)~ pregabalin. We claim: 1. A process for preparing (R)-(+)-3-