Enantioselective Total Synthesis of (1R,3S,4R,5R)-1-Amino-4,5-dihydroxycyclopentane-1,3-dicarboxylic Acid. A Full-Aldol Access to Carbaketose Derivatives-Reference-Cited by-同舟云学术

Enantioselective Total Synthesis of (1R,3S,4R,5R)-1-Amino-4,5-dihydroxycyclopentane-1,3-dicarboxylic Acid. A Full-Aldol Access to Carbaketose Derivatives

Published:2004-03-04 Issue:7 Volume:69 Page:2611-2613
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Battistini Lucia¹,Curti Claudio¹,Zanardi Franca¹,Rassu Gloria¹,Auzzas Luciana¹,Casiraghi Giovanni¹

Affiliation:

1. Dipartimento Farmaceutico, Università di Parma, Parco Area delle Scienze 27A, I-43100 Parma, Italy, and Istituto di Chimica Biomolecolare del CNR, Sezione di Sassari, Traversa La Crucca 3, I-07040 Li Punti, Sassari, Italy giovanni.casiraghi@unipr.it

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo035846a

Reference15 articles.

1. Mechanism for the opsin shift of retinal's absorption in bacteriorhodopsin

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3. Total Synthesis of Carba-d-fructofuranose via a Novel Metathesis Reaction

4. 1S,3R-ACPD-sensitive (metabotropic) [3H]glutamate receptor binding in membranes

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