Yamaguchi Esterification in the Synthetic Approaches to Precursors of Epothilone D Analogs
- Авторлар: Valeev R.F.1, Sunagatullina G.R.1, Miftakhov M.S.1
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Мекемелер:
- Ufa Institute of Organic Chemistry, Ufa Federal Research Center
- Шығарылым: Том 55, № 9 (2019)
- Беттер: 1439-1441
- Бөлім: Short Communications
- URL: https://journal-vniispk.ru/1070-4280/article/view/221235
- DOI: https://doi.org/10.1134/S1070428019090264
- ID: 221235
Дәйексөз келтіру
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.
Негізгі сөздер
Авторлар туралы
R. Valeev
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Хат алмасуға жауапты Автор.
Email: rusl0@yandex.ru
Ресей, Ufa, Bashkortostan
G. Sunagatullina
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Email: rusl0@yandex.ru
Ресей, Ufa, Bashkortostan
M. Miftakhov
Ufa Institute of Organic Chemistry, Ufa Federal Research Center
Email: rusl0@yandex.ru
Ресей, Ufa, Bashkortostan
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