Desymmetrisation of bicyclic, meso-anhydrides by proline esters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Asymmetric Desymmetrisation of Meso-Norbornene Anhydrides Utilising Methyl Prolinate as a Chiral Reagent
2. Desymmetrisation of meso-Anhydrides Utilising (S)-Proline Derivatives
3. Jones, I.G.; Jones, W.; North, M.; Synlett, accepted for publication.
4. A convenient synthesis of bridged azatricyclic anhydrides
5. Asymmetric Diels-Alder reaction. A facile route to chiral alkyl hydrogen cyclohexene-1,2-dicarboxylate
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1. Selective Carbon–Carbon Bond Cleavage of Cyclopropylamine Derivatives;Chemical Reviews;2020-06-22
2. Rhodium-Catalyzed Asymmetric Cyclization/Addition Reactions of 1,6-Enynes and Oxa/Azabenzonorbornadienes;Organic Letters;2018-02-13
3. Kinetic Resolution-Related PROCESSES;Key Chiral Auxiliary Applications;2014
4. Stereoselective synthesis of both enantiomers of trans-2-(diphenylmethylideneamino)cyclopropanecarboxylic acid using a chiral pool approach and their incorporation in dipeptides;Tetrahedron;2012-11
5. ChemInform Abstract: Desymmetrization of Bicyclic, meso-Anhydrides by Proline Esters.;ChemInform;2010-08-03
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