References
- Hoff BH, Anthonsen T. Lipase-catalyzed resolution of esters of 4-chloro-3-hydroxy-butanoic acid: Effects of the alkoxy group and solvent on the enantiomeric ratio. Tetrahed Asymm 1999; 10: 1401–1412
- Hollingsworth RI. 1998. Process for preparation of hydroxyl substituted gamma butyrolactones. US Patent 5,808,107, 15 Sept 1998.
- Kataoka M, Yamamoto K, Kawabata H, Wada M, Kika K, Yanase H, Shimizu S. Stereoselective reduction of ethyl 4-chloro-3-oxobutanoate by Escherichia coli transformant cells coexpressing the aldehyde reductase and glucose dehydrogenase genes. Appl Microbial Biotechnol 1999; 51: 486–490
- Kitamura M, Takaya O, Noyori R. A practical asymmetric synthesis of carnitine. Tetrahed Lett 1988; 29: 1555–1556
- Miyazawa K, Yoshida N. 1992. Process for producing optically active hydroxyl lactones. US Patent 5,084,392, 28 Jan 1992.
- Nakagawa A, Idogaki H, Kato K, Shinmyo A, Suzuki T. Improvement on production of (R)-4-chloro-3-hydroxybutyrate and (S)-3-hydroxy-γ-butyrolactone with recombinant Escherichia coli cells. J Biosci Bioeng 2006; 101: 97–103
- Pellegata R, Dosi I, Villa M, Lesma G, Palmisano G. (−)-β-Pinene as chiral promoter. Stereospecific access to (−)-γ-amino-β(R)-hydroxybutyric acid (GABOB) and (R)-carnitine. Tetrahedron 1985; 41: 5607–5613
- Santaniello E, Ferraboschi P, Grisenti P, Manzocchi A, Trave S. Studies on pig liver esterase-mediated hydrolyses of 3-hydroxy esters. Gazzetta Chim Ital 1989; 119: 581–584
- Suzuki T, Idogaki H, Kasai N. A novel generation of optically active ethyl 4-chloro-3-hydroxybutyrate as a C4 chiral building unit using microbial dechlorination. Tetrahed Asymm 1996; 7: 3109–3112
- Wang G, Hollingsworth RI. Synthetic routes to l-carnitine and l-gamma-amino-beta-hydroxybutyric acid from (S)-3-hydroxybutyrolactone by functional group priority switching. Tetrahed Asymm 1999; 10: 1895–1901
- Yamamoto H, Matsuyama A, Kobayashi Y. Synthesis of ethyl (R)-4-chloro-3-hydroxybutanoate with recombinant Escherichia coli cells expressing (S)-specific secondary alcohol dehydrogenase. Biosci Biotechnol Biochem 2002; 66: 481–483
- Yuasa Y, Tsuruta H. 1997. Practical syntheses of (S)-4-hydroxytetrahydrofuran-2-one, (S)-3-hydroxytetrahydrofuran and their (R)-enantiomers. Liebigs Ann IRecueil 1877–1879.
- Zhou BN, Gopalan AS, Van Middlesworth F, Shieh WR, Sih CJ. Stereochemical control of yeast reductions. l. Asymmetric synthesis of l-carnitine. J Am Chem Soc 1983; 105: 5925–5926