| Literature DB >> 22383859 |
Aleksandra Baranczak1, Gary A Sulikowski.
Abstract
A benzo[a]anthraquinone ring system, common to a group of angucycline antibiotics, has been prepared by a unique cascade of reactions. The reaction sequence was initiated by a Suzuki-Miyaura cross-coupling between a bromoquinone and vinyl boronic anhdyride. The reaction product is proposed to undergo a 6π-electron cyclization triggered by reductive activation of the quinone. The reaction process is proposed to be autocatalytic.Entities:
Year: 2012 PMID: 22383859 PMCID: PMC3287049 DOI: 10.1016/j.tetlet.2011.12.126
Source DB: PubMed Journal: Tetrahedron Lett ISSN: 0040-4039 Impact factor: 2.415