Загрузка...
Asymmetric Synthesis of the Core of AMPTD, the Key Amino Acid of Microsclerodermins F-I
We report a stereoselective synthesis of the five consecutive stereocenters of AMPTD in seven steps. Highlights include an Evans glycolate aldol reaction, the use of a Weinreb amide as an aldehyde masking group, and a Mannich reaction with an Ellman-type chiral sulfimine.
Сохранить в:
| Главные авторы: | , |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
2009
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2828631/ https://ncbi.nlm.nih.gov/pubmed/20191096 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|