New and old challenges in total synthesis. From concept to practice
S. Hanessian, R. Margarita, A. Hall, S. Johnstone, M. Tremblay, and L. Parlanti
Department of Chemistry, Université de Montréal,
P.O. Box 6128,
Station Centre-ville, Montréal, P.Q., H3C 3J Canada
Abstract: The total synthesis of dysinosin A, a novel
member of the aeruginosin group of marine natural products is discussed.
The stereocontrolled synthesis also confirms the proposed structure
and absolute stereochemistry of the natural product.
*Pure Appl.Chem. 75,
141�419 (2003). An issue of reviews and research papers based on
lectures presented at the 23rd IUPAC International Symposium on the
Chemistry of Natural Products, Florence, Italy, 28 July � 2 August 2002.
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