Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/4465
Title: A New Stereocontrolled Synthesys of Diidroxerulin, a Potent Noncytotoxic Inibithor of the Biosynthesis of Cholesterol
Authors: R., Rossi
F., Bellina
A., Catanese
L., Mannina
Valensin, Daniela 
Keywords: stereocontrol; furanones; lactonization; coupling reactions
Issue Date: 2000
Project: None 
Journal: TETRAHEDRON
Abstract: 
Dihydroxerulin, 1, has been stereoselectively synthesized by a convergent approach in which a key step was the Wittig reaction between (Z)-5-[(E)-3-formyl-2-propenylidene]-5H-furan-2-one 15, and the phosphonium ylid which derived from [(E)-2-decen-4,6-diyn-1-yl]triphenylphosphonium bromide, 19. Compound 19 was conveniently prepared by a short reaction sequence involving a Stille reaction between 1-trimethylstannyl-1,3-heptadiyne, 17, and (E)-3-iodo-2-propen-1-ol, 18. On the other hand, compound 15 was prepared in eight steps by a reaction sequence in which an immediate precursor to this butenolide, i.e. (Z)-5-[(2E)-4-hydroxy-2-butenylidene]-5H-furan-2-one, 34, was regio- and stereoselectively synthesized by AgO-catalysed lactonization of the corresponding (Z)-2-en-4-ynoic acid. The structure and stereochemistry of 1 were established on the basis of its H-1 and C-13 NMR spectra at 600 and 150 MHz, respectively, and by a combination of 2D NMR techniques. (C) 2000 Elsevier Science Ltd. All rights reserved.
Description: 
27086
URI: http://hdl.handle.net/20.500.12779/4465
ISSN: 0040-4020
DOI: 10.1016/S0040-4020(99)01030-3
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