Diastereo- and enantioselective syntheses of (−)-coniine, (−)-solenopsin A, (−)-solenopsis fugaz venom and (−)-xenovenine via deoxygenative decarboxylation of 2-carbonylsultam-substituted n-hydroxy-piperidines and -pyrrolidines-Reference-Cited by-同舟云学术

Diastereo- and enantioselective syntheses of (−)-coniine, (−)-solenopsin A, (−)-solenopsis fugaz venom and (−)-xenovenine via deoxygenative decarboxylation of 2-carbonylsultam-substituted n-hydroxy-piperidines and -pyrrolidines

Published:1994-09 Issue:38 Volume:35 Page:7015-7018
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Oppolzer Wolfgang,Bochet Christian G.,Merifield Eric

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Enantioselektive Synthesen chiraler Piperidinalkaloide

2. A New Approach to the Asymmetric Synthesis of Alkaloids

3. Synthesis of (?)-Pinidinevia asymmetric, electrophilic enolate hydroxyamination/nitrone reduction

4. Diastereo- and Enantiocontrolled Synthesis of (-)-Allosedaminevia Cycloaddition of a Chiral Nitrone

5. Asymmetric Synthesis of ?-Amino Acids and ?-N-Hydroxyamino Acids fromN-Acylbornane-10,2-sultams: 1-chloro-1-nitrosocyclohexane as a practical [NH2+] equivalent

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