1. Academic Validation
  2. Synthesis of Hemigossypol and its Derivatives

Synthesis of Hemigossypol and its Derivatives

  • Tetrahedron Lett. 2010 Oct 3;51(44):5757-5760. doi: 10.1016/j.tetlet.2010.08.089.
Jun Wei 1 David L Vander Jagt Robert E Royer Lorraine M Deck
Affiliations

Affiliation

  • 1 Department of Chemistry, University of New Mexico, Albuquerque, NM 87131.
Abstract

Hemigossypol (3), a sesquiterpene natural product, was previously isolated from Gossypium barbadense and was shown to display improved anti-fungal activity compared to gossypol (1), the disesquiterpene dimer of hemigossypol (3). Gossypol exhibits multiple biological activities. In order to study whether hemigossypol and it derivatives retain the various bioactivities of gossypol, we developed a short and convenient synthetic scheme to synthesize hemigossypol. This is the first de novo synthesis of this natural product. In addition derivatives of hemigossypol with various 2,5-alkyl substituents were synthesized. Modification of the synthetic scheme also afforded the natural product hemigossylic lactone (4) and its 2,5-substituted derivatives.

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