Cyclopropanol intermediates in the synthesis of the C5–C14 fragment of laulimalides


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Abstract

Two novel schemes have been developed for the synthesis of the C5–C14 fragment of the macrocyclic antitumor drug laulimalide and its analogs via transformations of cyclopropanol intermediates.

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I. V. Mineeva

Belarusian State University

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Email: i.mineyeva@yandex.ru
Russian Federation, pr. Nezavisimosti 4, Minsk, 220030

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