Affiliation:
1. Department of Chemistry, The Hong Kong University of Science and Technology, Clearwater Bay, Kowloon, Hong Kong, China
Abstract
The first collective total synthesis of sarglamides A, C, D, E, and F is achieved in 6–7 steps by exploiting the bio-inspired Diels–Alder reaction and one-pot reductive amination/aza-Michael addition or cycloetherification/transamination.
Funder
Research Grants Council, University Grants Committee
Publisher
Royal Society of Chemistry (RSC)