Use of the Intramolecular Aza-Wittig Reaction for the Access to 2-Cyclopropyl Cyclic Imines Which are Key Intermediates in the Synthesis of Bicyclic Alcaloids-Reference-Cited by-同舟云学术

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Use of the Intramolecular Aza-Wittig Reaction for the Access to 2-Cyclopropyl Cyclic Imines Which are Key Intermediates in the Synthesis of Bicyclic Alcaloids

Published:2010-09-01 Issue:7 Volume:94 Page:449-456
ISSN:0037-9646
Container-title:Bulletin des Sociétés Chimiques Belges
language:en
Short-container-title:Bull. Soc. Chim. Belges

Author:

Vaultier M.,Lambert P. H.,Carrié R.

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bscb.19850940703/fullpdf

Reference24 articles.

1. General methods of alkaloid synthesis

2. Cyclopropanone equivalents. Formation of 1-pyrrolizidione by a dicyclopropyl imine rearrangement.

3. Acid-catalyzed thermolysis of dicyclopropyl ketimines. Substituent effects on the course of the rearrangement

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1. Strategic approaches to the synthesis of pyrrolizidine and indolizidine alkaloids;Tetrahedron;2020-04

2. Tetrahydroazepines;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02

3. Asymmetric Aza-Wittig Reactions: Enantioselective Synthesis of β-Quaternary Azacycles;Angewandte Chemie International Edition;2006-07-24

4. Asymmetric Aza-Wittig Reactions: Enantioselective Synthesis of β-Quaternary Azacycles;Angewandte Chemie;2006-07-24

5. Synthesis of indolidines by the 1,3-dipolar cycloaddition of azides with methylenecyclopropanes followed by cyclopropyumine rearrangement;Tetrahedron Letters;1990-01

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