2-BROMO-3,4,4-TRICHLOROBUT-3-ENOATES OF CERTAIN NATURAL ALCOHOLS, PHENOLS, AND OXIMES OF CARBONYL COMPOUNDS

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Abstract

Previously undescribed 2-bromo-3,4,4-trichlorobut-3-enoates 1b-23b were synthesized in 84-91% yield from natural alcohols including terpenes and steroids, plant phenols, and oximes of natural carbonyl compounds 1a-23a by reaction of 2-bromo-3,4,4-trichlorobut-3-enoyl chloride in the presence of pyridine.

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