A Tandem Michael Addition Ring-Closure Route to the Metabotropic Receptor Ligand α-(Hydroxymethyl)glutamic Acid and Its γ-Alkylated Derivatives-Reference-Cited by-同舟云学术

A Tandem Michael Addition Ring-Closure Route to the Metabotropic Receptor Ligand α-(Hydroxymethyl)glutamic Acid and Its γ-Alkylated Derivatives

Published:2001-10-05 Issue:22 Volume:66 Page:7555-7559
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Zhang Jiazhong¹,Flippen-Anderson Judith L.¹,Kozikowski Alan P.¹

Affiliation:

1. Georgetown University Medical Center, Drug Discovery Program, 3970 Reservoir Road NW, Washington, D.C. 20007-2197, and Laboratory for the Structure of Matter, Code 6030, Naval Research Laboratory, 4555 Overlook Avenue SW, Washington, D.C. 20375-5000 kozikowa@georgetown.edu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010626n

Reference10 articles.

1. Ligands for Glutamate Receptors: Design and Therapeutic Prospects

2. Molecular Diversity of Glutamate Receptors and Implications for Brain Function

3. Stereoselektive Alkylierung an C(?) von Serin, Glycerins�ure, Threonin und Weins�ure �ber heterocyclische Enolate mit exocyclischer Doppelbindung

4. Unusual regiochemistry of cycloaddition of ketenes to (R)-2-tert-butyldihydrooxazole derivatives. A simple route towards enantiomerically pure functionalised α-aminocyclobutanones

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