Catalytic enantio- and diastereo-selective addition of diethylzinc to racemic α-thio- and α-seleno-aldehydes: asymmetric synthesis of optically active vicinal thio- and seleno-alcohols-Reference-Cited by-同舟云学术

Catalytic enantio- and diastereo-selective addition of diethylzinc to racemic α-thio- and α-seleno-aldehydes: asymmetric synthesis of optically active vicinal thio- and seleno-alcohols

Published:1993 Issue:18 Volume: Page:2193-2196
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Watanabe Makoto,Komota Mineo,Nishimura Masamichi,Araki Shuki,Butsugan Yasuo

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1993/P1/P19930002193

Reference22 articles.

1. General method for the synthesis of high enantiomeric purity chiral epoxides

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3. Highly stereoselective reduction of β-oxosulfonium salts ---synthesis of trans epoxides---

4. Preparation of 2-arylpropanoic acids by oxidative aryl migration in (β-aryl-β-hydroxy)alkyl phenyl selenides

5. 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

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