An alternative total synthesis of Aigialomycin D.

Autor: D G S, Sudhakar, Ch, Venkata Ramana Reddy, Syed, Tasqeeruddin, Sridhar, Gattu, Alapati, Srinivasa Rao
Předmět:
Zdroj: Synthetic Communications; 2024, Vol. 54 Issue 12, p992-998, 7p
Abstrakt: Aigialomycin D, a 14-membered benzannulated macrolactone, was synthesized in a simple, efficient and stereoselective approach using inexpensive and commonly accessible starting materials. The main steps in this convergent synthesis are Corey-Fuchs reaction, Yamaguchi esterification and ring closing metathesis (RCM). [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index