Artículos de revistas
A Morita-Baylis-Hillman adduct allows the diastereoselective synthesis of styryl lactones
Registration in:
Tetrahedron Letters. Pergamon-elsevier Science Ltd, v. 52, n. 46, n. 6180, n. 6184, 2011.
0040-4039
WOS:000296988700033
10.1016/j.tetlet.2011.09.044
Author
Paioti, PHS
Coelho, F
Institutions
Abstract
Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) We disclosed herein a diastereoselective approach for the total syntheses of (+/-)-Leiocarpin A and (+/-)-Goniodiol. These biologically active styryl lactones were obtained from a common intermediate, prepared in five steps and 40% overall yield, using a simple synthetic sequence starting from a Morita-Baylis-Hillman adduct. The total syntheses of these styryl lactones were accomplished in nine steps. This is the first report on the total synthesis of this class of natural products starting from Morita-Baylis-Hillman adduct. (C) 2011 Elsevier Ltd. All rights reserved. 52 46 6180 6184 Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
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