(±)-SEDAMINE AND (±)-ALLOSEDAMINE BY REDUTION OF N-METHYL-2-PHENACYLIDENEPIPER1DINE
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00304949609356556
Reference7 articles.
1. Sedum‐Alkaloide, III. Zur Konstitution des Sedinins
2. Chiral sulfur compounds. 9. Stereochemistry of the intermolecular and intramolecular conjugate additions of amines and anions to chiral (E)- and (Z)-vinyl sulfoxides. Total syntheses of (R)-(+)-carnegine and (+)- and (-)-sedamine
3. Ligand assisted hydride delivery : An expeditious stereoselective total synthesis of (±) nor-sedamine and its pyrrolidino analog
4. Stereoselective nucleophilic substitution of 6-methoxy-1-methoxycarbonylpipecolate: enantioselective synthesis of (+)-sedamine from L-lysine
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1. Synthesis of (−)-Sedinine by Allene Cyclization and Iminium Ion Chemistry;Organic Letters;2010-08-12
2. ChemInform Abstract: (.+-.)-Sedamine (VI) and (.+-.)-Allosedamine (VII) by Reduction of N- Methyl-2-phenacylidenepiperidine (IV).;ChemInform;2010-08-04
3. Studies on the Eschenmoser coupling reaction and insights on its mechanism. Application in the synthesis of Norallosedamine and other alkaloids;Tetrahedron;2009-03
4. (2E)-2-(1-Methylpiperidin-2-ylidene)-1-phenylethanone;Acta Crystallographica Section E Structure Reports Online;2006-12-06
5. Enantioselective Synthesis of (+)-Sedamine and (-)-Allosedamine;Synthesis;2006-12
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