Enantioface-differentiating Reactions Using (2S,2′S)-2-Hydroxymethyl-1-[(1-alkyl-2-pyrrolidinyl)methyl]pyrrolidines as Chiral Ligands. Addition of Lithium Derivatives of Methyl Phenyl Sulfide, Acetonitrile,N-Nitrosodimethylamine, and 2-Methylthiothiazoline to Aldehydes-Reference-Cited by-同舟云学术

Enantioface-differentiating Reactions Using (2S,2′S)-2-Hydroxymethyl-1-[(1-alkyl-2-pyrrolidinyl)methyl]pyrrolidines as Chiral Ligands. Addition of Lithium Derivatives of Methyl Phenyl Sulfide, Acetonitrile,N-Nitrosodimethylamine, and 2-Methylthiothiazoline to Aldehydes

Published:1979-11 Issue:11 Volume:52 Page:3371-3376
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Soai Kenso,Mukaiyama Teruaki

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/52/11/52_11_3371/_pdf

Reference28 articles.

1. Asymmetric reduction. Reduction of acetylenic ketones with chiral hydride agent

2. Asymmetric Reduction of Prochiral Ketones with Chiral Hydride Reagents Prepared from Lithium Aluminium Hydride and (S)-2-(N-Substituted aminomethyl)pyrrolidines

3. Herstellung von Hilfsstoffen für die asymmetrische Synthese aus Weinsäure. Addition von Butyllithium an Aldehyde in chiralem Medium

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