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SOAI, K., OYAMADA, H., YAMANOI, T. (1984) ChemInform Abstract: N,N′-DIBENZOYLCYSTINE AS AN EFFICIENT CHIRAL AUXILIARY FOR ASYMMETRIC REDUCTION OF KETONES WITH LITHIUM BOROHYDRIDE. Chemischer Informationsdienst, 15 (31) doi:10.1002/chin.198431182

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Reference TypeJournal (article/letter/editorial)
TitleChemInform Abstract: N,N′-DIBENZOYLCYSTINE AS AN EFFICIENT CHIRAL AUXILIARY FOR ASYMMETRIC REDUCTION OF KETONES WITH LITHIUM BOROHYDRIDE
JournalChemischer Informationsdienst
AuthorsSOAI, K.Author
OYAMADA, H.Author
YAMANOI, T.Author
Year1984 (July 31)Volume15
Issue31
PublisherWiley
DOIdoi:10.1002/chin.198431182Search in ResearchGate
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Mindat Ref. ID14891044Long-form Identifiermindat:1:5:14891044:9
GUID0
Full ReferenceSOAI, K., OYAMADA, H., YAMANOI, T. (1984) ChemInform Abstract: N,N′-DIBENZOYLCYSTINE AS AN EFFICIENT CHIRAL AUXILIARY FOR ASYMMETRIC REDUCTION OF KETONES WITH LITHIUM BOROHYDRIDE. Chemischer Informationsdienst, 15 (31) doi:10.1002/chin.198431182
Plain TextSOAI, K., OYAMADA, H., YAMANOI, T. (1984) ChemInform Abstract: N,N′-DIBENZOYLCYSTINE AS AN EFFICIENT CHIRAL AUXILIARY FOR ASYMMETRIC REDUCTION OF KETONES WITH LITHIUM BOROHYDRIDE. Chemischer Informationsdienst, 15 (31) doi:10.1002/chin.198431182
In(1984, July) Chemischer Informationsdienst Vol. 15 (31) Wiley

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SOAI, K., YAMANOI, T., OYAMADA, H. (1984) ChemInform Abstract: ASYMMETRIC REDUCTION OF ALKYL ARYL KETONES WITH LITHIUM BOROHYDRIDE USING N-BENZOYLCYSTEINE AS CHIRAL LIGAND. Chemischer Informationsdienst, 15 (31) doi:10.1002/chin.198431183
SOAI, K., YAMANOI, T., HIKIMA, H., OYAMADA, H. (1985) ChemInform Abstract: Asymmetric Reduction of Prochiral 3-Aryl-3-oxoesters with Lithium Borohydride Using N,N′-Dibenzoylcystine as a Chiral Auxiliary. Chemischer Informationsdienst, 16 (24) doi:10.1002/chin.198524169
SOAI, K., NIWA, S., YAMANOI, T., HIKIMA, H., ISHIZAKI, M. (1986) ChemInform Abstract: Asymmetrie Synthesis of 2-Aryl Substituted Oxetanes by Enantioselective Reduction of β-Halogenoketones Using Lithium Borohydride Modified with N,N′-Dibenzoylcystine. Chemischer Informationsdienst, 17 (49) doi:10.1002/chin.198649115
Soai, Kenso, Yamanoi, Takashi, Oyamada, Hidekazu (1984) ASYMMETRIC REDUCTION OF ALKYL ARYL KETONES WITH LITHIUM BOROHYDRIDE USINGN-BENZOYLCYSTEINE AS CHIRAL LIGAND. Chemistry Letters, 13 (2). 251-254 doi:10.1246/cl.1984.251
SOAI, K., OYAMADA, H., OOKAWA, A. (1982) ChemInform Abstract: SODIUM BOROHYDRIDE-TERT-BUTYL ALCOHOL-METHANOL AS AN EFFICIENT SYSTEM FOR THE SELECTIVE REDUCTION OF ESTERS. Chemischer Informationsdienst, 13 (47) doi:10.1002/chin.198247154
SOAI, K., YAMANOI, T., HIKIMA, H. (1985) ChemInform Abstract: ASYMMETRIC SYNTHESIS OF OPTICALLY ACTIVE HALOHYDRINS AND OXIRANES BY ENANTIOSELECTIVE REDUCTION OF PROCHIRAL α-HALOKETONES WITH CHIRALLY MODIFIED LITHIUM BOROHYDRIDE. Chemischer Informationsdienst, 16 (51) doi:10.1002/chin.198551168
SOAI, K., OYAMADA, H., TAKASE, M. (1984) ChemInform Abstract: THE PREPARATION OF N-PROTECTED AMINO ALCOHOLS AND N-PROTECTED PEPTIDE ALCOHOL BY REDUCTION OF THE CORRESPONDING ESTERS WITH SODIUM BOROHYDRIDE. AN IMPROVED PROCEDURE INVOLVING A SLOW ADDITION OF A SMALL AMOUNT OF METHANOL. Chemischer Informationsdienst, 15 (51) doi:10.1002/chin.198451156
SOAI, K., OOKAWA, A., OYAMADA, H., TAKASE, M. (1982) ChemInform Abstract: A NOVEL PROCEDURE FOR THE REDUCTION OF EPOXIDES WITH SODIUM BOROHYDRIDE. Chemischer Informationsdienst, 13 (52) doi:10.1002/chin.198252148
SOAI, K., OYAMADA, H. (1984) ChemInform Abstract: A CHEMOSELECTIVE ONE-STEP REDUCTION OF β-KETO ESTERS TO 1,3-DIOLS. Chemischer Informationsdienst, 15 (49) doi:10.1002/chin.198449119
SOAI, K., KOMIYA, K., SHIGEMATSU, Y., HASEGAWA, H., OOKAWA, A. (1983) ChemInform Abstract: UNUSUAL EFFECT OF A MIXED SOLVENT ON THE ASYMMETRIC REDUCTION OF CHIRAL α-KETO AMIDES WITH SODIUM BOROHYDRIDE. Chemischer Informationsdienst, 14 (15) doi:10.1002/chin.198315156
KITAZUME, T., YAMAZAKI, T., ISHIKAWA, N. (1984) ChemInform Abstract: ASYMMETRIC REDUCTION OF FLUORINATED KETONES AND KETO ESTERS WITH BAKERS′ YEAST. Chemischer Informationsdienst, 15 (4) doi:10.1002/chin.198404346
 
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