Yamaguchi Esterification in the Synthetic Approaches to Precursors of Epothilone D Analogs
- 作者: Valeev R.F.1, Sunagatullina G.R.1, Miftakhov M.S.1
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隶属关系:
- Ufa Institute of Organic Chemistry, Ufa Federal Research Center
- 期: 卷 55, 编号 9 (2019)
- 页面: 1439-1441
- 栏目: Short Communications
- URL: https://bakhtiniada.ru/1070-4280/article/view/221235
- DOI: https://doi.org/10.1134/S1070428019090264
- ID: 221235
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详细
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.
作者简介
R. Valeev
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
编辑信件的主要联系方式.
Email: rusl0@yandex.ru
俄罗斯联邦, Ufa, Bashkortostan
G. Sunagatullina
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Email: rusl0@yandex.ru
俄罗斯联邦, Ufa, Bashkortostan
M. Miftakhov
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Email: rusl0@yandex.ru
俄罗斯联邦, Ufa, Bashkortostan
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