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Chemistry and biology of diazonamide A: second total synthesis and biological investigations
Authors:Nicolaou K C  Hao Junliang  Reddy Mali V  Rao Paraselli Bheema  Rassias Gerasimos  Snyder Scott A  Huang Xianhai  Chen David Y-K  Brenzovich William E  Giuseppone Nicolas  O'Brate Aurora  Giannakakou Paraskevi
Affiliation:Contribution from the Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA. kcn@scripps.edu
Abstract:As an especially unique target for chemical synthesis, diazonamide A has the potential to be constructed through a plethora of synthetic routes, each attended by different challenges and opportunities for discovery. In this article, we detail our second total synthesis of diazonamide A through a sequence entirely distinct from that employed in our first campaign, one whose success required the development of several special strategies and tactics. We also disclose our complete studies regarding the chemical biology of diazonamide A and its structural congeners, and more fully delineate the scope of our protocol for Robinson-Gabriel cyclodehydration using pyridine-buffered POCl(3).
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