Аннотация:
The readily available Corey lactone was converted in three simple stages to tris-TBS-ether of (1R*,3R*,5S*)-1-hydroxymethyl-3,5-dihydroxy-2-methylidenecyclopentane – the protected carbocyclic core of Entecavir, one of the best medicines against hepatitis.
Реферативные базы данных:
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
Z. R. Valiullina, V. A. Akhmet'yanova, N. S. Vostrikov, M. S. Miftakhov, “A short synthesis of the carbocyclic core of Entecavir from Corey lactone”, Mendeleev Commun., 26:1 (2016), 9–10