| Literature DB >> 16468745 |
Ray T Syvitski1, Charles N Borissow, Cathy L Graham, David L Jakeman.
Abstract
[structure: see text] A novel oxazolone ring-opening and interconversion process between the two jadomycin diastereomeric forms has been characterized by NMR spectroscopy. An analogue, dalomycin T, has been isolated for the first time and does not undergo interconversion.Entities:
Mesh：
Substances：
Year: 2006 PMID： 16468745 DOI： 10.1021/ol052814w
Source DB: PubMed Journal: Org Lett ISSN： 1523-7052 Impact factor: 6.005