Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/20788
Title: Synthetic applications of chiral unsaturated epoxy alcohols prepared by sharpless asymmetric epoxidation
Author: Riera i Escalé, Antoni
Moreno, María
Keywords: Síntesi asimètrica
Epòxids
Alquens
Asymmetric synthesis
Epoxy compounds
Alkenes
Issue Date: 23-Feb-2010
Publisher: MDPI Publishing
Abstract: An overview of the synthesis and applications of chiral 2,3-epoxy alcohols containing unsaturated chains is presented. One of the fundamental synthetic routes to these compounds is Sharpless asymmetric epoxidation, which is reliable, highly chemoselective and enables easy prediction of the product enantioselectivity. Thus, unsaturated epoxy alcohols are readily obtained by selective oxidation of the allylic double bond in the presence of other carbon-carbon double or triple bonds. The wide availability of epoxy alcohols with unsaturated chains, the versatility of the epoxy alcohol functionality (e.g. regio- and stereo-selective ring opening; oxidation; and reduction), and the arsenal of established alkene chemistries, make unsaturated epoxy alcohols powerful starting materials for the synthesis of complex targets such as biologically active molecules. The popularization of ring-closing metathesis has further increased their value, making them excellent precursors to cyclic compounds.
Note: Reproducció del document publicat a: http://dx.doi.org/10.3390/molecules15021041
It is part of: Molecules 2010, 15(2), 1041-1073
URI: http://hdl.handle.net/2445/20788
ISSN: 1420-3049
Appears in Collections:Articles publicats en revistes (Institut de Recerca Biomèdica (IRB Barcelona))
Articles publicats en revistes (Química Inorgànica i Orgànica)

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