| Literature DB >> 15303893 |
K C Nicolaou1, Scott A Snyder, Nicolas Giuseppone, Xianhai Huang, Marco Bella, Mali V Reddy, Paraselli Bheema Rao, Alexandros E Koumbis, Aurora O'Brate, Paraskevi Giannakakou.
Abstract
In this article, we describe further studies toward the originally proposed structure of diazonamide A (1). After confronting a number of failures in synthesizing the heterocyclic core of that structure, success was finally realized through the development of a novel hetero-pinacol-based macrocyclization cascade sequence. Subsequent elaboration led to an advanced compound bearing both of the 12-membered rings of the target molecule. In addition, preliminary biological studies with intermediates and simplified analogues obtained via the developed sequences are also described.Entities:
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Year: 2004 PMID: 15303893 DOI: 10.1021/ja040091q
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419