Highly diastereoselactive synthesis of chimeras of proline and glutamate
Author:
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570430608/fullpdf
Reference19 articles.
1. Nouveaux acides amines libres de Afzelia bella: trans-hydroxy-4-L-proline et trans-carboxy-4-L-proline
2. Conformationally defined neurotransmitter analogs. Selective inhibition of glutamate uptake by one pyrrolidine-2,4-dicarboxylate diastereomer
3. Proline–Glutamate Chimeras in Isopeptides. Synthesis and Biological Evaluation of Conformationally Restricted Glutathione Analogues
4. Addition of tert-butylcuprate to (2S)-N-acyl-Δ5-dehydroprolinates as a diastereoselective synthetic procedure for obtaining (2S,5S)-5-tert-butylproline
5. Combinatorial Organic Synthesis of Highly Functionalized Pyrrolidines: Identification of a Potent Angiotensin Converting Enzyme Inhibitor from a Mercaptoacyl Proline Library
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