Carbon-Carbon Bond Formation by the Use of Chloroiodomethane as a C1Unit. IV. The Mannich Reaction of Ketones by Means of Dihalomethane and Secondary Amine-Reference-Cited by-同舟云学术

Carbon-Carbon Bond Formation by the Use of Chloroiodomethane as a C1Unit. IV. The Mannich Reaction of Ketones by Means of Dihalomethane and Secondary Amine

Published:1982-04 Issue:4 Volume:55 Page:1331-1332
ISSN:0009-2673
Container-title:Bulletin of the Chemical Society of Japan
language:en
Short-container-title:BCSJ

Author:

Miyano Sotaro,Mori Akira,Hokari Hiroshi,Ohta Katsuaki,Hashimoto Harukichi

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Link

https://www.jstage.jst.go.jp/article/bcsj1926/55/4/55_4_1331/_pdf

Reference9 articles.

1. Carbon-Carbon Bond Formation by the Use of Chloroiodomethane as a C1Unit. III. A Convenient Synthesis of the Mannich Base from Enol Silyl Ether by a Combination of Chloroiodomethane andN,N,N′,N′-Tetramethylmethanediamine

2. Carbon-Carbon Bond Formation by Use of Chloroiodomethane as a C1Unit. I. Formation of Chloromethyltriphenylphosphonium Iodide, and Its Application for the Wittig Chloromethylenation of Aldehydes and Ketones

3. Carbon–Carbon Bond Formation by the Use of Chloroiodomethane as a C1Unit. II. The Preparation and Synthetic Application of 1-Chloro-3-iodoheptane

4. Method for the regiospecific synthesis of Mannich bases. Reaction of enol borinates with dimethyl(methylene)ammonium iodide

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