Unusual ring opening of a Cyclopropylideneamine derivative during a favorskii-type rearrangement of α-Chloroketimines-Reference-Cited by-同舟云学术

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Unusual ring opening of a Cyclopropylideneamine derivative during a favorskii-type rearrangement of α-Chloroketimines

Published:1986-01 Issue:1 Volume:42 Page:71-80
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

De Kimpe Norbert,Palamareva Mariana,Sulmon Paul,Verhe Roland,De Buyck Laurent,Schamp Niceas,Declerco Jean-Paul,Tinant Bernard,Van Meerssche Maurice

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. The Favorskii Rearrangement

2. Favorskii rearrangements. Evidence for steric control in the fission of crowded cyclopropanone intermediates

3. Allene epoxidation. Isolation of a cyclopropanone

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1. Sodium-iodoxybenzoate mediated highly chemoselective aziridination of olefins;Tetrahedron;2014-09

2. Highly Regioselective Transformation of Alkenyl Bromides into α-Bromoaziridines and α-Bromohydrazones;Organic Letters;2006-04-13

3. The Favorskii Rearrangement: Synthetic Applications;Current Organic Chemistry;2005-11-01

4. 1-Azaallylic Anions in Heterocyclic Chemistry;Chemical Reviews;2004-04-17

5. Synthesis of cis,cis,cis-Tetrasubstituted Cyclobutanes. Trapping of Tetrahedral Intermediates in Intramolecular Nucleophilic Addition;The Journal of Organic Chemistry;2000-09-14

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