Email this article Yamaguchi Esterification in the Synthetic Approaches to Precursors of Epothilone D Analogs
- Authors: Valeev R.F.1, Sunagatullina G.R.1, Miftakhov M.S.1
-
Affiliations:
- Ufa Institute of Organic Chemistry, Ufa Federal Research Center
- Issue: Vol 55, No 9 (2019)
- Pages: 1439-1441
- Section: Short Communications
- URL: https://bakhtiniada.ru/1070-4280/article/view/221235
- DOI: https://doi.org/10.1134/S1070428019090264
- ID: 221235
Cite item
Open Access
Access granted
Subscription Access
Abstract
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.
About the authors
R. F. Valeev
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Author for correspondence.
Email: rusl0@yandex.ru
Russian Federation, Ufa, Bashkortostan
G. R. Sunagatullina
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Email: rusl0@yandex.ru
Russian Federation, Ufa, Bashkortostan
M. S. Miftakhov
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Email: rusl0@yandex.ru
Russian Federation, Ufa, Bashkortostan
Supplementary files
