A stereoselective approach to the angucyclinone antibiotics: A total synthesis of (±)-urdamycinone B

A stereoselective chiral Lewis acid promoted reaction of siloxydiene (±)-13 and dienophile complex 18, gave a 4:1 mixture of urdamycinone B (1) and its C-3 epimer (24) in several steps in 12% overall yield. Separation of these products was achieved by high performance liquid chromatography (HPLC). K...

Full description

Bibliographic Details
Main Authors: Hasnah Osman, David S. Larsen, Akkarapalli Muralikrishna
Format: Article
Language:English
Published: Elsevier 2019-12-01
Series:Arabian Journal of Chemistry
Online Access:http://www.sciencedirect.com/science/article/pii/S1878535215001240