The Regio- and Stereoselective Synthesis oftrans-2,3-DihydropyridineN-oxides and Piperidines-Reference-Cited by-同舟云学术

The Regio- and Stereoselective Synthesis oftrans-2,3-DihydropyridineN-oxides and Piperidines

Published:2009-04-20 Issue:18 Volume:48 Page:3288-3291
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Andersson Hans,Gustafsson Magnus,Boström Dan,Olsson Roger,Almqvist Fredrik

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference28 articles.

1. Reactions of aryl Grignard reagents with pyridine 1-oxide. Structure of the addition products

2. Grignard-Addition an Pyridin-N-oxid

3. Ring-opening does not occur when 3- or 3,5-methylpyridine N-oxide is reacted with Grignard reagents, instead pyridines are formed. See reference [3a].

4. Complexation Promoted Additions to N-Benzoyliminopyridinium Ylides. A Novel and Highly Regioselective Approach to Polysubstituted Piperidines

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