The 1,3-Dipolar Cycloaddition Reactions of Heteroaromatic Dicyanomethylides with Phenylsulfinylethene and Bis(trimethylsilyl)ethyne: Synthesis of 1,2-Unsunstituted 3-Cyanoindolizines

DOI: 10.1246/bcsj.60.3645

Source and publish data:

Bulletin of the Chemical Society of Japan p. 3645 - 3654 (1987)

Update date:2022-07-30

Topics:

Authors:

Matsumoto, Kiyoshi

Uchida, Takane

Ikemi, Yukio

Tanaka, Toshio

Asahi, Momoyo

et al. et al.

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Article abstract of DOI:10.1246/bcsj.60.3645

Pyridinium and diazinium dicycanomethylides underwent 1,3-dipolar cycloaddition-extrusion reactions with phenylsulfinylethene, producing the corresponding 3-cyanoindolizines in moderate to good yields. 1,3-Dipolar cycloadditions of these ylides with bis(t

Full text of DOI:10.1246/bcsj.60.3645

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