ChemInform Abstract: Optically Active Alcohols: Resolution and Synthesis from Asymmetric Reduction of Prochiral Ketones

10.1002/chin.200017258 ◽

2010 ◽

Vol 31 (17) ◽

pp. no-no

Author(s):

Xian-ming Hu ◽

Jun Liu

Keyword(s):

Asymmetric Reduction ◽

Optically Active ◽

Prochiral Ketones

Download Full-text

Optically active alcohols: Resolution and synthesis from asymmetric reduction of prochiral ketones

Wuhan University Journal of Natural Sciences ◽

10.1007/bf02841502 ◽

1999 ◽

Vol 4 (2) ◽

pp. 205-210 ◽

Author(s):

Hu Xian-ming ◽

Liu Jun

Keyword(s):

Asymmetric Reduction ◽

Optically Active ◽

Prochiral Ketones

Download Full-text

ASYMMETRIC REDUCTION OF PROCHIRAL KETONES WITH A CHIRAL REDUCING AGENT PREPARED FROM STANNOUS CHLORIDE, CHIRAL DIAMINE AS A LIGAND, AND DIISOBUTYLALUMINUM HYDRIDE

Chemistry Letters ◽

10.1246/cl.1984.2071 ◽

1984 ◽

Vol 13 (12) ◽

pp. 2071-2074 ◽

Author(s):

Takeshi Oriyama ◽

Teruaki Mukaiyama

Keyword(s):

Stannous Chloride ◽

Asymmetric Reduction ◽

Reducing Agent ◽

Diisobutylaluminum Hydride ◽

Chiral Diamine ◽

Prochiral Ketones

Download Full-text

ChemInform Abstract: Selective Reductions. Part 45. Asymmetric Reduction of Prochiral Ketones by Iso-2-methyl-, Iso-2-ethyl-, and (Iso-2-(2-(benzyloxy)ethyl)apopinocampheyl)-tert-butylchloroboranes. Evidence for a Major Influence of the Steric Requirement

10.1002/chin.199008085 ◽

1990 ◽

Vol 21 (8) ◽

Author(s):

H. C. BROWN ◽

P. V. RAMACHANDRAN

Keyword(s):

Asymmetric Reduction ◽

Major Influence ◽

Prochiral Ketones

Download Full-text

ChemInform Abstract: ASYMMETRIC CATALYSES, 14. ENANTIOSELECTIVE HYDROSILYLATION OF PROCHIRAL KETONES WITH RHODIUM AND PLATINUM COMPLEXES OF OPTICALLY ACTIVE NITROGEN CHELATE LIGANDS

Chemischer Informationsdienst ◽

10.1002/chin.198427082 ◽

1984 ◽

Vol 15 (27) ◽

Author(s):

H. BRUNNER ◽

B. REITER ◽

G. RIEPL

Keyword(s):

Platinum Complexes ◽

Optically Active ◽

Active Nitrogen ◽

Chelate Ligands ◽

Prochiral Ketones

Download Full-text

Asymmetric reduction of prochiral ketones by cell-free systems fromalcaligenes eutrophus

Journal of Chemical Technology & Biotechnology ◽

10.1002/jctb.280590307 ◽

1994 ◽

Vol 59 (3) ◽

pp. 249-255 ◽

Author(s):

Kattigere M. Madyastha ◽

Tarikere L. Gururaja

Keyword(s):

Asymmetric Reduction ◽

Prochiral Ketones

Download Full-text

(2S)-2-Anilinomethylpyrrolidine: an efficient in situ recyclable chiral catalytic source for the borane-mediated asymmetric reduction of prochiral ketones in refluxing toluene

Tetrahedron Asymmetry ◽

10.1016/j.tetasy.2006.03.021 ◽

2006 ◽

Vol 17 (7) ◽

pp. 1041-1044 ◽

Author(s):

Deevi Basavaiah ◽

Kalapala Venkateswara Rao ◽

Bhavanam Sekhara Reddy

Keyword(s):

Asymmetric Reduction ◽

Prochiral Ketones

Download Full-text

Enantioselective synthesis of optically active β-aminoalcohols via asymmetric reduction

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)80269-4 ◽

1992 ◽

Vol 3 (3) ◽

pp. 341-342 ◽

Author(s):

Byung Tae Cho ◽

Yu Sung Chun

Keyword(s):

Asymmetric Reduction ◽

Optically Active ◽

Enantioselective Synthesis

Download Full-text

An Asymmetric Reduction of Prochiral Ketones with a Chiral Hydride Reagent Prepared from Lithium Aluminium Hydride and (S)-2-(2,6-Xylidinomethyl)pyrrolidine

Heterocycles ◽

10.3987/r-1979-04-0499 ◽

1979 ◽

Vol 12 (4) ◽

pp. 499 ◽

Author(s):

Teruaki Mukaiyama ◽

Masatoshi Asami

Keyword(s):

Asymmetric Reduction ◽

Lithium Aluminium Hydride ◽

Lithium Aluminium ◽

Prochiral Ketones

Download Full-text

ChemInform Abstract: ASYMMETRIC REDUCTION OF PROCHIRAL KETONES WITH A CHIRAL REDUCING AGENT PREPARED FROM STANNOUS CHLORIDE, CHIRAL DIAMINE AS A LIGAND, AND DIISOBUTYLALUMINUM HYDRIDE

Chemischer Informationsdienst ◽

10.1002/chin.198524122 ◽

1985 ◽

Vol 16 (24) ◽

Author(s):

T. ORIYAMA ◽

T. MUKAIYAMA

Keyword(s):

Stannous Chloride ◽

Asymmetric Reduction ◽

Reducing Agent ◽

Diisobutylaluminum Hydride ◽

Chiral Diamine ◽

Prochiral Ketones

Download Full-text

Asymmetric Reactions. IV. An Attempted Asymmetric Reduction by a Solution of [Co(CN)5]3−and Optically Active α-Amino Acid, and Its Reactive Species

Bulletin of the Chemical Society of Japan ◽

10.1246/bcsj.43.505 ◽

1970 ◽

Vol 43 (2) ◽

pp. 505-509 ◽

Author(s):

Yoshiaki Ohgo ◽

Seiji Takeuchi ◽

Juji Yoshimura

Keyword(s):

Asymmetric Reduction ◽

Reactive Species ◽

Optically Active ◽

Asymmetric Reactions

Download Full-text