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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.

About the authors

I. V. Mineeva

Belarusian State University

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

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