jo049806y_si_002.cif (23.24 kB)

Synthesis of Putative Uniflorine A

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posted on 30.04.2004 by Andrew S. Davis, Stephen G. Pyne, Brian W. Skelton, Allan H. White
A diastereoselective synthesis of the putative structure of the natural product uniflorine A has been achieved by using the Petasis borono−Mannich reaction and ring-closing metathesis as key steps. The NMR data of the synthetic material did not match that reported for the natural product. The structure of the final synthetic product was unequivocally determined by single-crystal X-ray study of its pentaacetate derivative. Thus it was concluded that the proposed structure of uniflorine A is incorrect.