Cycloadditions of trifluoroacetonitrile oxide with olefins and acetylenes.

K Tanaka, H Masuda, K Mitsuhashi

Index: Tanaka; Masuda; Mitsuhashi Bulletin of the Chemical Society of Japan, 1984 , vol. 57, # 8 p. 2184 - 2187

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Citation Number: 40

Abstract

The regio-and stereoselectivity of the cydoadditions of trifluoroacetonitrile oxide (1) with olefins and acetylenes were described. The oxide 1, generated in situ from trifluoroacetohydroximoyl bromide etherate in the presence of triethylamine, reacted with various monosubstituted olefins and acetylenes to give exclusively 5-substituted 3- trifluoromethyl-2-isoxazolines and-isoxazoles, respectively, whereas 1 cyclized with 1, 2- ...

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