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A general organocatalyst for direct alpha-functionalization of aldehydes: Stereoselective C-C, C-N, C-F, C-BR, and C-S bond-forming reactions. Scope and mechanistic insights
Vise andre og tillknytning
2005 (engelsk)Inngår i: Journal of the American Chemical Society, ISSN 0002-7863, E-ISSN 1520-5126, Vol. 127, nr 51, s. 18296-18304Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The development of a general organocatalyst for the alpha-functionalization of aldehydes, via an enamine intermediate, is presented. Based on optically active alpha,alpha-diarylprolinol silyl ethers, the scope and applications of this catalyst for the stereogenic formation of C-C, C-N, C-F, C-Br, and C-S bonds are outlined. The reactions all proceed in good to high yields and with excellent enantioselectivities. Furthermore, we will present mechanistic insight into the reaction course applying nonlinear effect studies, kinetic resolution, and computational investigations leading to an understanding of the properties of the alpha,alpha-diarylprolinol silyl ether catalysts.

sted, utgiver, år, opplag, sider
2005. Vol. 127, nr 51, s. 18296-18304
Emneord [en]
asymmetric aldol reactions, amino-acid-derivatives, mannich-type reactions, enantioselective synthesis, michael reactions, alpha, alpha-disubstituted aldehydes, alpha, beta-unsaturated aldehydes, 1, 2-amino alcohols, enamine catalysis, l-prolinamide
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Identifikatorer
URN: urn:nbn:se:kth:diva-15285DOI: 10.1021/ja056120uISI: 000234258700062OAI: oai:DiVA.org:kth-15285DiVA, id: diva2:333326
Merknad
QC 20100525Tilgjengelig fra: 2010-08-05 Laget: 2010-08-05 Sist oppdatert: 2017-12-12bibliografisk kontrollert

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Franzen, Johan.
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