A Direct Reduction of Aliphatic Aldehyde, Acyl Chloride, Ester, and Carboxylic Functions into a Methyl Group-Reference-Cited by-同舟云学术

A Direct Reduction of Aliphatic Aldehyde, Acyl Chloride, Ester, and Carboxylic Functions into a Methyl Group

Published:2001-02-08 Issue:5 Volume:66 Page:1672-1675
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gevorgyan Vladimir¹,Rubin Michael¹,Liu Jian-Xiu¹,Yamamoto Yoshinori¹

Affiliation:

1. Department of Chemistry, University of Illinois at Chicago, 845 W. Taylor Street, Chicago, Illinois 60607-7061, and Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001258a

Reference14 articles.

1. A new facile diastereoconversion of 2-amino alcohols involving a novel cyclocarbamation

2. Tris(pentafluorophenyl)boron-Catalyzed Hydrosilation of Aromatic Aldehydes, Ketones, and Esters

3. Studies on the Mechanism of B(C6F5)3-Catalyzed Hydrosilation of Carbonyl Functions

4. A novel reduction of alcohols and ethers with a HSiEt3catalytic B(C6F5)3 system

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