Tetrahedron

Asymmetric synthesis of phosphonic acid analogues for acylcarnitine

T Yamagishi, K Fujii, S Shibuya, T Yokomatsu

Index: Yamagishi, Takehiro; Fujii, Keiichi; Shibuya, Shiroshi; Yokomatsu, Tsutomu Tetrahedron, 2006 , vol. 62, # 1 p. 54 - 65

Full Text: HTML

Citation Number: 15

Abstract

Phosphonic acid analogues of acylcarnitine were prepared in an optically active form expecting CPT I inhibitory activities. The synthetic methodology was based on catalytic asymmetric dihydroxylation of β, γ-unsaturated phosphonates and subsequent regioselective amination via the cyclic sulfates.

Related Articles:

Desulfinylation of prop-2-enesulfinic acid: Experimental results and mechanistic theoretical analysis

[Fokin, Andrey A.; Yurchenko, Alexander G.; Rodionov, Vladimir N.; Gunchenko, Pavel A.; Yurchenko, Raisa I.; Reichenberg, Armin; Wiesner, Jochen; Hintz, Martin; Jomaa, Hassan; Schreiner, Peter R. Organic Letters, 2007 , vol. 9, # 21 p. 4379 - 4382]

More Articles...