Diastereoselective, large scale synthesis of β-amino acids via asymmetric enamide hydrogenation as α2δ ligands for the treatment of generalized anxiety disorder and insomnia-Reference-Cited by-同舟云学术

Diastereoselective, large scale synthesis of β-amino acids via asymmetric enamide hydrogenation as α2δ ligands for the treatment of generalized anxiety disorder and insomnia

Published:2009-11 Issue:46 Volume:50 Page:6329-6331
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Magano Javier,Conway Brian,Bowles Daniel,Nelson Jade,Nanninga Thomas N.,Winkle Derick D.,Wu Haifeng,Chen Michael H.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference20 articles.

1. Magano, J.; Bowles, D.; Conway, B.; Nelson, J.; Nanninga, T. N.; Winkle, D. D. See preceding Letter.

2. Copper‐Catalyzed Enantioselective Conjugate Addition of Grignard Reagents to α,β‐Unsaturated Esters

3. Further studies on the substrate spectrum of phytanoyl-CoA hydroxylase

4. A Safe, Economical Method for the Preparation of β-Oxo Esters

5. Expeditious, large scale preparation of ethyl (R)-5-methyl-3-oxo octanoate via a cross Claisen reaction between N-acyl oxazolidinone derivatives and the magnesium enolate of potassium ethyl malonate

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