Issue 20, 1992

Total synthesis of (±)-fredericamycin A. Use of radical spirocyclization

Abstract

(±)-Fredericamycin A 1 is synthesized using 5-exo-digonal radical closure of selenide 15(Scheme 2), and an unusual procedure for both selective demethylation of the advanced intermediate 22 and adjustment of the stereochemistry in the pentadienyl side chain.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1992, 1489-1490

Total synthesis of (±)-fredericamycin A. Use of radical spirocyclization

D. L. J. Clive, Y. Tao, A. Khodabocus, Y. Wu, A. G. Angoh, S. M. Bennett, C. N. Boddy, L. Bordeleau, D. Kellner, G. Kleiner, D. S. Middleton, C. J. Nichols, S. R. Richardson and P. G. Vernon, J. Chem. Soc., Chem. Commun., 1992, 1489 DOI: 10.1039/C39920001489

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