-
1
-
-
33845552079
-
Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitine
-
Zhou B., Gopalan A.S., VanMiddlesworth F., Shieh W.-R., Sih C.J. Stereochemical control of yeast reductions. 1. Asymmetric synthesis of L-carnitine. J. Am. Chem. Soc. 105:1983;5925-5926.
-
(1983)
J. Am. Chem. Soc.
, vol.105
, pp. 5925-5926
-
-
Zhou, B.1
Gopalan, A.S.2
Vanmiddlesworth, F.3
Shieh, W.-R.4
Sih, C.J.5
-
3
-
-
0026599226
-
An efficient synthesis of (R)-carnitine
-
Kasai N., Sakaguchi K. An efficient synthesis of (R)-carnitine. Tetrahedr. Lett. 33:1992;1211-1212.
-
(1992)
Tetrahedr. Lett.
, vol.33
, pp. 1211-1212
-
-
Kasai, N.1
Sakaguchi, K.2
-
4
-
-
0019191883
-
Total synthesis of (R)-glycerol acetonide and the antiepileptic and hypotensive drug (-)-γ-amino-β-hydroxybutyric acid (GABOB). Use of vitamin C as a chiral starting material
-
Jung M.E., Shaw T.J. Total synthesis of (R)-glycerol acetonide and the antiepileptic and hypotensive drug (-)-γ-amino-β-hydroxybutyric acid (GABOB). Use of vitamin C as a chiral starting material. J. Am. Chem. Soc. 102:1980;6304-6311.
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 6304-6311
-
-
Jung, M.E.1
Shaw, T.J.2
-
5
-
-
0021053906
-
Synthesis of S- And R-4-amino-3-hydroxybutyric acid (GABOB) and S- And R-carnitine from arabinose or ascorbic acid
-
Bock K., Lundt I., Pedersen C. Synthesis of S- and R-4-amino-3-hydroxybutyric acid (GABOB) and S- and R-carnitine from arabinose or ascorbic acid. Acta Chem. Scand. B. 37:1983;341-344.
-
(1983)
Acta Chem. Scand. B.
, vol.37
, pp. 341-344
-
-
Bock, K.1
Lundt, I.2
Pedersen, C.3
-
6
-
-
0000830198
-
Asymmetric epoxidation of homoallylic alcohols. Synthesis of (-)-γ-amino-β(R)-hydroxybutyric acid (GABOB)
-
Rossiter B.E., Sharpless K.B. Asymmetric epoxidation of homoallylic alcohols. Synthesis of (-)-γ-amino-β(R)-hydroxybutyric acid (GABOB). J. Org. Chem. 49:1984;3707-3711.
-
(1984)
J. Org. Chem.
, vol.49
, pp. 3707-3711
-
-
Rossiter, B.E.1
Sharpless, K.B.2
-
7
-
-
0017395379
-
Cyclic GABA-GABOB analogues. I. Synthesis of new 4-hydroxy-2-pyrrolinone derivatives
-
Pifferi G., Pinza M. Cyclic GABA-GABOB analogues. I. Synthesis of new 4-hydroxy-2-pyrrolinone derivatives. Farmaco. Ed. Sci. 32:1977;602-613.
-
(1977)
Farmaco. Ed. Sci.
, vol.32
, pp. 602-613
-
-
Pifferi, G.1
Pinza, M.2
-
8
-
-
84993879121
-
An improved syntheses of γ-, δ-, and ε-lactums
-
Pellegata R., Pinza M., Pifferi G. An improved syntheses of γ-, δ-, and ε-lactums. Synthesis. 1978;614-616.
-
(1978)
Synthesis
, pp. 614-616
-
-
Pellegata, R.1
Pinza, M.2
Pifferi, G.3
-
9
-
-
0000494506
-
Chiral synthesis of a component of Amanita muscaria, (-)-4-hydroxypyrrolidone-2-one, and assessment of its absolute configuration
-
Santaniello E., Casati R., Milani F. Chiral synthesis of a component of Amanita muscaria, (-)-4-hydroxypyrrolidone-2-one, and assessment of its absolute configuration. J. Chem. Res (S). 1984;132-133.
-
(1984)
J. Chem. Res (S)
, pp. 132-133
-
-
Santaniello, E.1
Casati, R.2
Milani, F.3
-
10
-
-
0345362242
-
Bioconversion of L-carnitine precursors by yeast
-
Hubert J.B., Jacques P., Bare G., Dewulf O., Thonart P. Bioconversion of L-carnitine precursors by yeast. Medet. Fac. Landbowwet. Rijuksuniv. Gent. 54:1989;1287-1300.
-
(1989)
Medet. Fac. Landbowwet. Rijuksuniv. Gent.
, vol.54
, pp. 1287-1300
-
-
Hubert, J.B.1
Jacques, P.2
Bare, G.3
Dewulf, O.4
Thonart, P.5
-
11
-
-
0024987854
-
Microbial asymmetric reduction of ethyl 4-chloro-3-oxobutanoate to optically active ethyl 4-chloro-3-hydroxybutanoate
-
Shimizu S., Kataoka M., Morishita A., Katoh M., Morikawa T., Miyoshi T., Yamada H. Microbial asymmetric reduction of ethyl 4-chloro-3-oxobutanoate to optically active ethyl 4-chloro-3-hydroxybutanoate. Biotechnol. Lett. 12:1990;593-596.
-
(1990)
Biotechnol. Lett.
, vol.12
, pp. 593-596
-
-
Shimizu, S.1
Kataoka, M.2
Morishita, A.3
Katoh, M.4
Morikawa, T.5
Miyoshi, T.6
Yamada, H.7
-
12
-
-
0026128595
-
Bioconversion of an L-carnitine precursor in a one- Or two-phase system
-
Bare G., Jaques P., Hubert J.B., Rikir R., Thonart P. Bioconversion of an L-carnitine precursor in a one- or two-phase system. Appl. Biochem. Biotechnol. 28-29:1991;445-456.
-
(1991)
Appl. Biochem. Biotechnol.
, vol.2829
, pp. 445-456
-
-
Bare, G.1
Jaques, P.2
Hubert, J.B.3
Rikir, R.4
Thonart, P.5
-
13
-
-
0028891152
-
Yeast-catalysed reduction of β-keto esters. 1. Factors affecting whole-cell catalytic activity and stereoselectivity
-
Hunt J.R., Carter A.S., Murrell J.C., Dalton H., Hallinan K.O., Crout D.H.G., Holt R.A., Crosby J. Yeast-catalysed reduction of β-keto esters. 1. Factors affecting whole-cell catalytic activity and stereoselectivity. Biocatal. Biotransform. 12:1995;159-178.
-
(1995)
Biocatal. Biotransform.
, vol.12
, pp. 159-178
-
-
Hunt, J.R.1
Carter, A.S.2
Murrell, J.C.3
Dalton, H.4
Hallinan, K.O.5
Crout, D.H.G.6
Holt, R.A.7
Crosby, J.8
-
14
-
-
0028888771
-
Yeast catalysed reduction of β-keto esters. 2. Optimisation of the stereospecific reduction by Zygosaccharomyces rouxii
-
Hallinan K.O., Crout D.H.G., Hunt J.R., Carter A.S., Dalton H., Murrell J.C., Holt R.A., Crosby J. Yeast catalysed reduction of β-keto esters. 2. Optimisation of the stereospecific reduction by Zygosaccharomyces rouxii. Biocatal. Biotransform. 12:1995;179-191.
-
(1995)
Biocatal. Biotransform.
, vol.12
, pp. 179-191
-
-
Hallinan, K.O.1
Crout, D.H.G.2
Hunt, J.R.3
Carter, A.S.4
Dalton, H.5
Murrell, J.C.6
Holt, R.A.7
Crosby, J.8
-
15
-
-
0030575817
-
A novel generation of optically active ethyl 4-chloro-3-hydroxybutyrate as a C4 chiral building unit using microbial dechlorination
-
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. Tetrahedr. Asym. 11:1996;3109-3112.
-
(1996)
Tetrahedr. Asym.
, vol.11
, pp. 3109-3112
-
-
Suzuki, T.1
Idogaki, H.2
Kasai, N.3
-
16
-
-
0025766920
-
Convenient preparation of BINAP-Ruthenium (II) complexes catalyzing asymmetric hydrogenation of functionalized ketones
-
Kitamura M., Tokunaga M., Ohkuma T., Noyori R. Convenient preparation of BINAP-Ruthenium (II) complexes catalyzing asymmetric hydrogenation of functionalized ketones. Tetrahedr. Lett. 32:1991;4163-4166.
-
(1991)
Tetrahedr. Lett.
, vol.32
, pp. 4163-4166
-
-
Kitamura, M.1
Tokunaga, M.2
Ohkuma, T.3
Noyori, R.4
-
17
-
-
0030200770
-
Aymmetric synthesis of (+)-negamycin
-
Davies S.G., Ichihara O. Aymmetric synthesis of (+)-negamycin. Tetrahedr. Asym. 7:1996;1919-1922.
-
(1996)
Tetrahedr. Asym.
, vol.7
, pp. 1919-1922
-
-
Davies, S.G.1
Ichihara, O.2
-
18
-
-
0344816143
-
Synthesis of (S)-N-(benzyloxy)-4-acetoxymethyl-2-azetidinone, potential intermediate for carbapenem antibiotics, by chemomicrobiological approach
-
Yamada H., Sugiyama H., Kajiwara M. Synthesis of (S)-N-(benzyloxy)-4-acetoxymethyl-2-azetidinone, potential intermediate for carbapenem antibiotics, by chemomicrobiological approach. Heterocycles. 26:1987;2841-2844.
-
(1987)
Heterocycles
, vol.26
, pp. 2841-2844
-
-
Yamada, H.1
Sugiyama, H.2
Kajiwara, M.3
-
19
-
-
0038903219
-
A stereospecific synthesis of optically pure (-)-α-Multistriatin
-
Larcheveque L., Henrot S. A stereospecific synthesis of optically pure (-)-α-Multistriatin. Tetrahedron. 43:1987;2303-2310.
-
(1987)
Tetrahedron
, vol.43
, pp. 2303-2310
-
-
Larcheveque, L.1
Henrot, S.2
-
20
-
-
0018429424
-
Synthesis of optically active forms of ipsdienol and ipsenol
-
Mori K., Takigawa T., Matsuo T. Synthesis of optically active forms of ipsdienol and ipsenol. Tetrahedron. 35:1979;933-940.
-
(1979)
Tetrahedron
, vol.35
, pp. 933-940
-
-
Mori, K.1
Takigawa, T.2
Matsuo, T.3
-
21
-
-
0000749329
-
Combination of borane-dimethyl sulfide complex with catalytic sodium teterahydroborate as a selective reducing agent for α-hydroxy esters, versatile chiral building block from (S)-(-)-malic acid
-
Saito S., Hasegawa T., Inaba M., Nishida R., Fujii T., Nomizu S., Moriwake T. Combination of borane-dimethyl sulfide complex with catalytic sodium teterahydroborate as a selective reducing agent for α-hydroxy esters, versatile chiral building block from (S)-(-)-malic acid. Chem. Lett. 1984;1389-1392.
-
(1984)
Chem. Lett.
, pp. 1389-1392
-
-
Saito, S.1
Hasegawa, T.2
Inaba, M.3
Nishida, R.4
Fujii, T.5
Nomizu, S.6
Moriwake, T.7
-
22
-
-
85008080870
-
A novel synthesis of (R)- And (S)-4-hydroxytetrahydrofuran-2-ones
-
Tanaka A., Yamashita K. A novel synthesis of (R)- and (S)-4-hydroxytetrahydrofuran-2-ones. Synthesis. 1987;570-573.
-
(1987)
Synthesis
, pp. 570-573
-
-
Tanaka, A.1
Yamashita, K.2
-
23
-
-
0000402818
-
Amino acids as chiral synthons: Preparation of enantiomerically pure (R)- And (S)-malic acids and its application to the synthesis of 3-hydroxy-4-butanolide
-
Henrot S., Larcheveque M., Petit Y. Amino acids as chiral synthons Preparation of enantiomerically pure (R)- and (S)-malic acids and its application to the synthesis of 3-hydroxy-4-butanolide . Syn. Commun. 16:1986;183-190.
-
(1986)
Syn. Commun.
, vol.16
, pp. 183-190
-
-
Henrot, S.1
Larcheveque, M.2
Petit, Y.3
-
24
-
-
84987439915
-
(R)-Ethyl 4-t-butoxy-3-hydroxybutanoate, a versatile chiral building block for EPC (enantiomerically pure compound) syntheses, by yeast reduction of ethyl 4-t-butoxy-3-oxobutanoate
-
Seebach D., Eberle M. (R)-Ethyl 4-t-butoxy-3-hydroxybutanoate, a versatile chiral building block for EPC (enantiomerically pure compound) syntheses, by yeast reduction of ethyl 4-t-butoxy-3-oxobutanoate. Synthesis. 1986;37-40.
-
(1986)
Synthesis
, pp. 37-40
-
-
Seebach, D.1
Eberle, M.2
-
25
-
-
0003900798
-
Single step conversion of chiral carnitine and derivatives into (S)- And (R)-β-substituted-γ-butyrolactones
-
Calvisi G., Catini R., Chiariotti W., Giannessi F., Muck S., Tinti O., Angelis F.D. Single step conversion of chiral carnitine and derivatives into (S)- and (R)-β-substituted-γ-butyrolactones. Synlett. 1997;71-74.
-
(1997)
Synlett
, pp. 71-74
-
-
Calvisi, G.1
Catini, R.2
Chiariotti, W.3
Giannessi, F.4
Muck, S.5
Tinti, O.6
Angelis, F.D.7
-
26
-
-
84954911534
-
Degradation of 2,3-dichloro-1-propanol by a Pseudomonas
-
Kasai N., Tsujimura K., Unoura K., Suzuki T. Degradation of 2,3-dichloro-1-propanol by a Pseudomonas. Agric. Biol. Chem. 54:1990;3185-3190.
-
(1990)
Agric. Biol. Chem.
, vol.54
, pp. 3185-3190
-
-
Kasai, N.1
Tsujimura, K.2
Unoura, K.3
Suzuki, T.4
-
27
-
-
0026816532
-
Preparation of (S)-2,3-dichloro-1-propanol by Pseudomonas sp. and its use in the synthesis of (R)-epichlorohydrin
-
Kasai N., Tsujimura K., Unoura K., Suzuki T. Preparation of (S)-2,3-dichloro-1-propanol by Pseudomonas sp. and its use in the synthesis of (R)-epichlorohydrin. J. Ind. Microbiol. 9:1992;97-101.
-
(1992)
J. Ind. Microbiol.
, vol.9
, pp. 97-101
-
-
Kasai, N.1
Tsujimura, K.2
Unoura, K.3
Suzuki, T.4
-
28
-
-
0026896825
-
Isolation of (S)-2,3-dichloro-1-propanol assimilating bacterium, its characterization, and its use in preparation of (R)-2,3-dichloro-1-propanol and (S)-epichlorohydrin
-
Kasai N., Tsujimura K., Unoura K., Suzuki T. Isolation of (S)-2,3-dichloro-1-propanol assimilating bacterium, its characterization, and its use in preparation of (R)-2,3-dichloro-1-propanol and (S)-epichlorohydrin. J. Ind. Microbiol. 10:1992;37-43.
-
(1992)
J. Ind. Microbiol.
, vol.10
, pp. 37-43
-
-
Kasai, N.1
Tsujimura, K.2
Unoura, K.3
Suzuki, T.4
-
29
-
-
0001762455
-
Ueber die Abhängigkeit der verschiedenen Vertretbarkeit des Radicalwasserstoffs in den isomeren Buttersäuren
-
Markonikoff W.I. Ueber die Abhängigkeit der verschiedenen Vertretbarkeit des Radicalwasserstoffs in den isomeren Buttersäuren. Liebigs. Ann. Chem. 153:1870;228-259.
-
(1870)
Liebigs. Ann. Chem.
, vol.153
, pp. 228-259
-
-
Markonikoff, W.I.1
-
30
-
-
0026639091
-
Isolation of a bacterium assimilating (R)-3-chloro-1,2-propanediol and production of (S)-3-chloro-1,2-propanediol using microbial resolution
-
Suzuki T., Kasai N., Yamamoto R., Minamiura N. Isolation of a bacterium assimilating (R)-3-chloro-1,2-propanediol and production of (S)-3-chloro-1,2-propanediol using microbial resolution. J. Ferment. Bioeng. 73:1992;443-448.
-
(1992)
J. Ferment. Bioeng.
, vol.73
, pp. 443-448
-
-
Suzuki, T.1
Kasai, N.2
Yamamoto, R.3
Minamiura, N.4
-
32
-
-
0000660620
-
Oxidation of unsaturated compounds. II. Preparation and configuration of the 3-halogeno derivatives of crotonic acid
-
Braun G. Oxidation of unsaturated compounds. II. Preparation and configuration of the 3-halogeno derivatives of crotonic acid. J. Am. Chem. Soc. 52:1930;3167-3176.
-
(1930)
J. Am. Chem. Soc.
, vol.52
, pp. 3167-3176
-
-
Braun, G.1
-
33
-
-
0005152232
-
Classification and identification of aerobic bacteria
-
T. Hasegawa. Tokyo: Gakkai Syuppan Center
-
Komagata K. Classification and identification of aerobic bacteria. Hasegawa T. Classification and Identification of Microorganisms. 1981;203-245 Gakkai Syuppan Center, Tokyo.
-
(1981)
Classification and Identification of Microorganisms
, pp. 203-245
-
-
Komagata, K.1
-
34
-
-
0000803252
-
Gram-negative aerobic rods and cocci
-
Krieg N.R. 9th Ed. Baltimore: Williams & Wilkins
-
Brinley-Morgan W.J., Ley D.J., Dye D.W., Larsen H., Vincent J.M., Whittenbury R. Gram-negative aerobic rods and cocci. Krieg N.R. 9th Ed. Bergey's Manual of Systematic Bacteriology. Vol. 1:1984;140-407 Williams & Wilkins, Baltimore.
-
(1984)
Bergey's Manual of Systematic Bacteriology
, vol.1
, pp. 140-407
-
-
Brinley-Morgan, W.J.1
Ley, D.J.2
Dye, D.W.3
Larsen, H.4
Vincent, J.M.5
Whittenbury, R.6
-
35
-
-
0344068723
-
Application for bacteriology
-
K. Amako, Koike M. Tokyo: Gakken Shuppan Center
-
Amako K. Application for bacteriology. Amako K., Koike M. Electron Microscopy in Microbiology. Vol. 1:1982;23-26 Gakken Shuppan Center, Tokyo.
-
(1982)
Electron Microscopy in Microbiology
, vol.1
, pp. 23-26
-
-
Amako, K.1
-
36
-
-
0001606804
-
New colorimetric determination of chloride using mercuric thiocyanate and ferric ion
-
Iwasaki I., Utsumi S., Ozawa T. New colorimetric determination of chloride using mercuric thiocyanate and ferric ion. Bull. Chem. Soc. Jpn. 25:1952;226.
-
(1952)
Bull. Chem. Soc. Jpn.
, vol.25
, pp. 226
-
-
Iwasaki, I.1
Utsumi, S.2
Ozawa, T.3
-
39
-
-
0023875288
-
Microbial and enzymatic processes for the production of biologically and chemically useful compounds
-
Yamada H., Shimizu S. Microbial and enzymatic processes for the production of biologically and chemically useful compounds. Angew. Chem. Int. Ed. Engl. 27:1988;622-642.
-
(1988)
Angew. Chem. Int. Ed. Engl.
, vol.27
, pp. 622-642
-
-
Yamada, H.1
Shimizu, S.2
-
40
-
-
0025281564
-
Stereoselective reduction of 4-chloro-3-oxo-butanoate by a microbial aldehyde-reductase in an organic solvent-water diphasic system
-
Shimizu S., Kataoka M., Katoh M., Morikawa T., Miyoshi T., Yamada H. Stereoselective reduction of 4-chloro-3-oxo-butanoate by a microbial aldehyde-reductase in an organic solvent-water diphasic system. Appl. Environ. Microbiol. 56:1990;2374-2377.
-
(1990)
Appl. Environ. Microbiol.
, vol.56
, pp. 2374-2377
-
-
Shimizu, S.1
Kataoka, M.2
Katoh, M.3
Morikawa, T.4
Miyoshi, T.5
Yamada, H.6
-
42
-
-
0344068721
-
Synthesis of optically active 4-hydroxytetrahydrofuran-2-on and 3-hydroxytetrahydrofuran
-
Yuasa, Y., Sotoguchi, T., Kumobayashi, H., and Tsuruta, N. Synthesis of optically active 4-hydroxytetrahydrofuran-2-on and 3-hydroxytetrahydrofuran. Abstract of Annual Meeting of the Pharmaceutical Society of Japan, 1997, 45.
-
(1997)
Abstract of Annual Meeting of the Pharmaceutical Society of Japan
, pp. 45
-
-
Yuasa, Y.1
Sotoguchi, T.2
Kumobayashi, H.3
Tsuruta, N.4
-
43
-
-
0000436236
-
Lipase catalyzed synthesis of macrocyclic lactones in organic solvent
-
Makita A., Nihira T., Yamada Y. Lipase catalyzed synthesis of macrocyclic lactones in organic solvent. Tetrahedr. Lett. 28:1987;805-808.
-
(1987)
Tetrahedr. Lett.
, vol.28
, pp. 805-808
-
-
Makita, A.1
Nihira, T.2
Yamada, Y.3
-
44
-
-
0025645837
-
Lipase-catalyzed synthesis of macrocyclic lactones in organic solvents
-
Kageyama Y., Nihira T., Yamada Y. Lipase-catalyzed synthesis of macrocyclic lactones in organic solvents. Ann. N. Y. Acad. Sci. 613:1990;681-685.
-
(1990)
Ann. N. Y. Acad. Sci.
, vol.613
, pp. 681-685
-
-
Kageyama, Y.1
Nihira, T.2
Yamada, Y.3
-
45
-
-
0025952672
-
Purification, characterization, and molecular cloning of lactonizing lipase from Pseudomonas sp
-
Ihara F., Kageyama Y., Hirata M., Nihira T., Yamada Y. Purification, characterization, and molecular cloning of lactonizing lipase from Pseudomonas sp. J. Biol. Chem. 299:1991;18135-18140.
-
(1991)
J. Biol. Chem.
, vol.299
, pp. 18135-18140
-
-
Ihara, F.1
Kageyama, Y.2
Hirata, M.3
Nihira, T.4
Yamada, Y.5
-
46
-
-
0000098355
-
Degradation of epichlorohydrin and halohydrins by bacterial cultures isolated from freshwater sediment
-
van den Wijngaard A.J., Janssen D.B., Witholt B. Degradation of epichlorohydrin and halohydrins by bacterial cultures isolated from freshwater sediment. J. Gen. Microbiol. 135:1989;2199-2208.
-
(1989)
J. Gen. Microbiol.
, vol.135
, pp. 2199-2208
-
-
Van Den Wijngaard, A.J.1
Janssen, D.B.2
Witholt, B.3
-
47
-
-
0026004141
-
Purification and characterization of haloalcohol dehalogenase from Arthrobacter sp. strain AD2
-
van den Wijngaard A.J., Reuvekamp P.T.W., Janssen D.B. Purification and characterization of haloalcohol dehalogenase from Arthrobacter sp. strain AD2. J. Bacteriol. 173:1991;124-129.
-
(1991)
J. Bacteriol.
, vol.173
, pp. 124-129
-
-
Van Den Wijngaard, A.J.1
Reuvekamp, P.T.W.2
Janssen, D.B.3
-
48
-
-
0026446815
-
Resolution and some properties of enzyme involved in enantioselective transformation of 1,3-dichloro-2-propanol to (R)-3-chloro-1,2-propanediol by Corynebacterium sp. strain N-1704
-
Nakamura T., Nagasawa T., Yu F., Watanabe I., Yamada H. Resolution and some properties of enzyme involved in enantioselective transformation of 1,3-dichloro-2-propanol to (R)-3-chloro-1,2-propanediol by Corynebacterium sp. strain N-1704. J. Bacteriol. 174:1992;7613-7619.
-
(1992)
J. Bacteriol.
, vol.174
, pp. 7613-7619
-
-
Nakamura, T.1
Nagasawa, T.2
Yu, F.3
Watanabe, I.4
Yamada, H.5
-
49
-
-
0028344820
-
A novel generation of optically active 1,2-diols from the racemates by using halohydrin dehydro-dehalogenase
-
Suzuki T., Kasai N., Minamiura N. A novel generation of optically active 1,2-diols from the racemates by using halohydrin dehydro-dehalogenase. Tetrahed. Asym. 5:1994;239-246.
-
(1994)
Tetrahed. Asym.
, vol.5
, pp. 239-246
-
-
Suzuki, T.1
Kasai, N.2
Minamiura, N.3
|