General Reactivity of 2-Lithiobenzothiazole to Various Electrophiles and the Use as a Formyl Anion Equivalent in the Synthesis of α-Hydroxy Carbonyl Compounds-Reference-Cited by-同舟云学术

General Reactivity of 2-Lithiobenzothiazole to Various Electrophiles and the Use as a Formyl Anion Equivalent in the Synthesis of α-Hydroxy Carbonyl Compounds

Published:1988-10 Issue:10 Volume:61 Page:3637-3648
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Chikashita Hidenori,Ishibaba Megumi,Ori Keiji,Itoh Kazuyoshi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/61/10/61_10_3637/_pdf

Reference9 articles.

1. Methods of Reactivity Umpolung

2. Carbanions of 1,3-Dithianes. Reagents for CC Bond Formation by Nucleophilic Displacement and Carbonyl Addition

3. Syntheses via-2-oxazolines. I. Formylation of Grignard reagents in the presence of hexamethylphosphoramide

4. Reactions of Organometallic Compounds with Benzothiazoles

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