Highly Diastereoselective Michael Addition Reactions of Butane-2,3-diacetal Desymmetrized Glycolic Acid. Preparation of α-Hydroxy-γ-amino Acid Derivatives-Reference-Cited by-同舟云学术

Highly Diastereoselective Michael Addition Reactions of Butane-2,3-diacetal Desymmetrized Glycolic Acid. Preparation of α-Hydroxy-γ-amino Acid Derivatives

Published:2001-10-19 Issue:23 Volume:3 Page:3753-3755
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Dixon Darren J.¹,Ley Steven V.¹,Rodríguez Félix¹

Affiliation:

1. Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol016708f

Reference17 articles.

1. α‐Hydroxy Acids in Enantioselective Syntheses

2. 3-Alkyl-4-aminobutyric acids: the first class of anticonvulsant agents that activates L-glutamic acid decarboxylase

3. Stereospecific binding of the antidepressant rolipram to brain protein structures

4. 4-Amino-hex-5-enoic Acid, a Selective Catalytic Inhibitor of 4-Aminobutyric-Acid Aminotransferase in Mammalian Brain

5. The Outstanding Biological Stability ofβ- andγ-Peptides toward Proteolytic Enzymes: An In Vitro Investigation with Fifteen Peptidases

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