| Literature DB >> 31287955 |
Halima Bagum1, Kirsten E Christensen1, Miroslav Genov2, Alexander Pretsch2, Dagmar Pretsch2, Mark G Moloney1,3.
Abstract
A general route which provides direct access to pyroglutamates from tetramates, making use of Suzuki coupling on an enol mesylate, followed by reduction, is reported. This work permits direct scaffold hopping from tetramate to substituted pyroglutamates. Some compounds in the library showed modest antibacterial activity against Gram-positive bacteria.Entities:
Year: 2019 PMID: 31287955 DOI: 10.1021/acs.joc.9b01432
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354