Highly Stereoselective Michael Addition Reactions of CamTHP*-Desymmetrized Glycinamide for the Synthesis of Functionally Dense Amino Acid Derivatives-Reference-Cited by-同舟云学术

Highly Stereoselective Michael Addition Reactions of CamTHP*-Desymmetrized Glycinamide for the Synthesis of Functionally Dense Amino Acid Derivatives

Published:2004-10-26 Issue:24 Volume:6 Page:4427-4429
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Dixon Darren J.¹,Horan Richard A. J.¹,Monck Nathaniel J. T.¹,Berg Paul¹

Affiliation:

1. Department of Chemistry, University of Manchester, Manchester, M13 9PL, U,K., Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K., and Vernalis plc, Oakdene Court, 613 Reading Road, Winnersh, Wokingham RG41 5UA, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol048568q

Reference13 articles.

1. Enzyme Inhibition by Amino Acids and their Derivatives

2. (a) Wehbe, J.; Rolland, V.; Roumestant, M. L.; Martinez, J.Tetrahedron: Asymmetry2003,14, 1123 and references therein.

3. (c) Hruby, V. J.; Sharma, S. D.; Collins, N.; Matsunaga, T. O.; Russell, K. C InSynthetic Peptides: A User's Guide; Grant, G. A., Ed.; W. H. Freeman and Co. New York, 1992; p 259.

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