An efficient stereoselective synthesis of methyl (S)-3-amino-3-(3-pyridyl)propanoate-Reference-Cited by-同舟云学术

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An efficient stereoselective synthesis of methyl (S)-3-amino-3-(3-pyridyl)propanoate

Published:1999-10 Issue:44 Volume:40 Page:7721-7725
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Marlon Zhong H,Cohen Judith H,Abdel-Magid Ahmed F,Kenney Birdella D,Maryanoff Cynthia A,Shah Rekha D,Villani Frank J,Zhang Fan,Zhang Xini

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Costanzo, M. J.; Hoekstra, W. J.; Maryanoff, B. E. PCT Appl. WO 98/50575, 1998.

2. Enantioselective Synthesis of β-Amino Acids;Pedrosa,1996

3. Asymmetric Michael reactions of 3,5-dihydro-4H-dinaphth[2,1-c:1',2'-e]azepine with methyl crotonate

4. An asymmetric ammonia synthon for Michael additions

5. A highly stereoselective Michael addition to an .alpha.,.beta.-unsaturated ester as the crucial step in the synthesis of a novel .beta.-amino acid-containing fibrinogen receptor antagonist

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