Yamaguchi Esterification in the Synthetic Approaches to Precursors of Epothilone D Analogs
- Авторы: Valeev R.F.1, Sunagatullina G.R.1, Miftakhov M.S.1
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Учреждения:
- Ufa Institute of Organic Chemistry, Ufa Federal Research Center
- Выпуск: Том 55, № 9 (2019)
- Страницы: 1439-1441
- Раздел: Short Communications
- URL: https://bakhtiniada.ru/1070-4280/article/view/221235
- DOI: https://doi.org/10.1134/S1070428019090264
- ID: 221235
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Аннотация
Coupling of previously synthesized chiral building blocks via Yamaguchi esterification has been studied with the goal of obtaining epothilone D isosteres. Some peculiar features of the Yamaguchi esterification stage have been revealed, which are related to the reactivity and molecular structure of the initial acid and alcohol components.
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Об авторах
R. Valeev
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Автор, ответственный за переписку.
Email: rusl0@yandex.ru
Россия, Ufa, Bashkortostan
G. Sunagatullina
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Email: rusl0@yandex.ru
Россия, Ufa, Bashkortostan
M. Miftakhov
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Email: rusl0@yandex.ru
Россия, Ufa, Bashkortostan
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