An Efficient and General Method for the Reformatsky-Type Reaction of Chlorodifluoromethyl Ketones with Carbonyl Compounds Giving α,α-Difluoro-β-hydroxy Ketones-Reference-Cited by-同舟云学术

An Efficient and General Method for the Reformatsky-Type Reaction of Chlorodifluoromethyl Ketones with Carbonyl Compounds Giving α,α-Difluoro-β-hydroxy Ketones

Published:1990-02 Issue:2 Volume:63 Page:428-437
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Kuroboshi Manabu,Ishihara Takashi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/63/2/63_2_428/_pdf

Reference50 articles.

1. Zinc-copper(I) chloride or -silver(I) acetate promoted aldol reaction of chlorodifluoromethyl ketones with carbonyl compounds. A general and effective route to α,α-difuluoro-β-hydroxy ketones

2. Metal enolates in organic synthesis

3. Highly selective re-additions to a masked oxaloacetate. Absolute configurations of fluorocitric acids

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