From 3-aza-2-oxobicyclo[3.1.0]hexane to enantiopure disubstituted cyclopropane: a convenient approach to cis-2,3-methano-GABA
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
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1. Synthesis, Structural Insights and Activity of Different Classes of Biomolecules;The First Outstanding 50 Years of “Università Politecnica delle Marche”;2020
2. Four Stereoisomers of 2-Aminomethyl-1-cyclopropanecarboxylic Acid: Synthesis and Biological Evaluation;Bulletin of the Chemical Society of Japan;2019-11-15
3. Synthesis of Racemic 2‐(Aminomethyl)cyclopropane‐1,1‐dicarboxylic Acid as a New Constrained γ‐Amino Dicarboxylic Acid Bypassing Alkyl 3‐Aza‐2‐oxobicyclo[3.1.0]hexane‐1‐carboxylates;European Journal of Organic Chemistry;2019-06-13
4. Practical Syntheses of Both Enantiomers of the Conformationally Restricted GABA Analoguecis-(2-Aminocyclobutyl)acetic Acid;European Journal of Organic Chemistry;2014-09-25
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