Reductive Ring Opening of Ephedrine and Pseudo-Ephedrine-Derived Oxazolidinium Methiodides by Sodium Borohydride. A Direct Access to New Chiral Amine-Borane Adducts-Reference-Cited by-同舟云学术

Reductive Ring Opening of Ephedrine and Pseudo-Ephedrine-Derived Oxazolidinium Methiodides by Sodium Borohydride. A Direct Access to New Chiral Amine-Borane Adducts

Published:1992-03 Issue:6 Volume:22 Page:829-839
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Andres Celia,Delgado Manuel,Pedrosa Rafael

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

http://www.tandfonline.com/doi/pdf/10.1080/00397919208020847

Reference25 articles.

1. Brown, H. C. and Jadhav, P. K. 1983.Asymmetric Synthesis, Edited by: Morrison, J. D. vol. 2, 1London: Academic.

2. Asymmetric induction. Part 3. Asymmetric reduction of ketones with amine-boranes in the presence of acids

3. Asymmetric reduction of N-substituted ketimines with the reagent prepared from borane and (S)-(–)-2-amino-3-methyl-1,1-diphenylbutan-1-ol (itsuno's reagent): enantioselective synthesis of optically active secondary amines

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