Reaction of cyclopropane carboxylic acid derivatives with sulphur tetrafluoride—an example of a diastereoselective ring opening

Z Hell, Z Finta, W Dmowski, F Faigl, YM Pustovit…

Index: Hell; Finta; Dmowski; Faigl; Pustovit; Toke; Harmat Journal of Fluorine Chemistry, 2000 , vol. 104, # 2 p. 297 - 301

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Citation Number: 7

Abstract

Cyclopropane carboxylic acid derivatives can be converted into trifluoromethyl group- containing compounds using SF4. In the case of a bicyclic cyclopropane carboxylic acid lactone, similar treatment with sulphur tetrafluoride resulted in the cyclopropane ring opening in a diastereoselective manner.