Chiral cyclic β-amino esters. Part II: Synthesis by diastereoselective reduction of enamino esters
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Chiral cyclic β-amino esters. Part I: Synthesis by diastereospecific alkylation
2. Imidoylation Reaction: (±)-Lupinine Synthesis
3. Enantiodivergent synthesis of (+)- and (-)-anatoxin from L-glutamic acid
4. Enantiospecific Synthesis of (+)- and (−)-Ferruginine from l-Glutamic Acid. Synthesis of Tropanes via Intramolecular Iminium Ion Cyclization
5. Asymmetric synthesis with chiral hydrogenolysable amines. Cyclic β-enamino ester reduction a diastereoselective route to 2,3-disubstituted pyrrolidines
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1. Chiral Phosphinyl Enamines and Their Asymmetric Reduction through Group-Assisted Purification Chemistry Leading to Enantiopure β-Amino Esters/Amides;Synlett;2017-08-04
2. Practical, Asymmetric Route to Sitagliptin and Derivatives: Development and Origin of Diastereoselectivity;Organic Letters;2015-03-23
3. Asymmetric syntheses of dihydroxyhomoprolines via doubly diastereoselective lithium amide conjugate addition reactions;Tetrahedron;2013-10
4. FeCl3-PTSA Co-Catalysed Highly Regio- and Stereo-Selective Synthesis of β-Functionalised Enamine Derivatives;Journal of Chemical Research;2012-03
5. Cyanuric chloride catalysed rapid conversion of β-ketoesters into β-enaminoesters under mild and solvent-free conditions;Journal of the Iranian Chemical Society;2011-09
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