Controlled reduction of 5-alkyl-3-phenyl-2,3,5,6,7,8-hexahydro-oxazolo[3,2-a]pyridin-4-ylium iodide: enantioselective synthesis of (−)-dihydropinidine and (+)-indolizidine 167B-Reference-Cited by-同舟云学术

Controlled reduction of 5-alkyl-3-phenyl-2,3,5,6,7,8-hexahydro-oxazolo[3,2-a]pyridin-4-ylium iodide: enantioselective synthesis of (−)-dihydropinidine and (+)-indolizidine 167B

Published:2004-11 Issue:21 Volume:15 Page:3393-3395
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Roa Luis F.,Gnecco Dino,Galindo Alberto,Terán Joel L.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference14 articles.

1. Syntheses of pyridin-4-ylium chirons: applications in a synthesis of (+)-coniine

2. Selective Reductions of 1-Methyl-4-phenyl-2-pyridone

3. New methodology for the synthesis of enantiopure (3R,2aR)-(−)-3-phenyl-hexahydro-oxazolo[3,2-a]-pyridin-5-one: a synthesis of (S)-(+)-coniine

4. Preparation of Optically Active 6-Substituted 2-Piperidones by Oxidation of the Corresponding Oxazolopiperidines.

5. A New Approach to the Asymmetric Synthesis of Carbacephams

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