On the synthesis of pyrinodemin A. Part 1: The location of the olefin
SP Romeril, V Lee, JE Baldwin, TDW Claridge
Index: Romeril, Stuart P.; Lee, Victor; Baldwin, Jack E.; Claridge, Timothy D.W. Tetrahedron, 2005 , vol. 61, # 5 p. 1127 - 1140
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Citation Number: 10
Abstract
The elucidation of the structure of the cytotoxic marine sponge alkaloid pyrinodemin A by synthesis is described. Based on the 13C NMR spectra of three double bond positional isomers and the natural product, it is concluded the C14′–C15′ isomer best represents the true structure of pyrinodemin A. In addition, the structural assignment of pyrinodemin C is evaluated.
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