The imine-epoxide rearrangement in the formation of trans-2,6-disubstituted piperidines. A stereoselective synthesis of (±)-teneraic acid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Synthesis of 2,6-disubstituted piperidines, oxanes, and thianes
2. Hydrogenation of Derivatives of Pyridine
3. Stereoselective synthesis of 1-substituted 2,6-dicyanopiperidines and transformation of 2,6-dialkylated products of 1-phenyl-2,6-dicyanopiperidine to .delta.-diketones and cyclohexenones
4. Stereoselective syntheses of solenopsin A and B
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1. Stereo-Selective Preparation of Teneraic Acid, trans-(2S,6S)-Piperidine-2,6-dicarboxylic Acid, via Anodic Oxidation and Cobalt-Catalyzed Carbonylation;Chemical and Pharmaceutical Bulletin;2017
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4. Efficient synthesis of cis-2,6-di-(2-quinolylpiperidine);Tetrahedron Letters;2013-09
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