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Enantioselective α-heterofunctionalisation of carbonyl compounds:: organocatalysis is the simplest approach

Journal

TETRAHEDRON-ASYMMETRY
Volume 17, Issue 10, Pages 1465-1492

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2006.05.020

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Enantioselective organocatalytic processes have reached maturity in recent years with an impressive number of applications now available. The application of these advantageous methodologies to the construction of chiral alpha-hetereofunctionalised carbonyl compounds allows us to obtain important chiral building blocks, such as a-amino acids, alpha-amino alcohols, aziridines, epoxides, 1,2-diols and alpha-sulfenylated, selenenylated and halogenated carbonyl derivatives. Proline, imidazolidinone derivatives, cinchona alkaloids and their ammonium salts, as well as Bronsted acid derivatives, have been used as chiral catalysts for these purposes. A survey of contributions in this field will be discussed throughout this review. (c) 2006 Elsevier Ltd. All rights reserved.

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