| Literature DB >> 26465962 |
David E Williams1, Helen Bottriell1, Julian Davies2, Ian Tietjen3, Mark A Brockman3,4, Raymond J Andersen1.
Abstract
Unciaphenol (2), an oxygenated analogue of the Bergman cyclization product of the enediyne uncialamycin (1), has been isolated along with 1 from cultures of the actinomycete Streptomyces uncialis. It is proposed that the C-22 OH substituent in 2 might arise from the attack of a nucleophilic oxygen species on the p-benzyne diradical intermediate IA in the Bergman cyclization of 1. 2 shows in vitro anti-HIV activity against viral strains that are resistant to clinically utilized anti-retroviral therapies.Entities:
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Year: 2015 PMID: 26465962 DOI: 10.1021/acs.orglett.5b02664
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005