Synthesis of functionalised azepanes and piperidines from bicyclic halogenated aminocyclopropane derivatives
Author:
Affiliation:
1. Laboratoire de Synthèse Organique (LSO)
2. UMR 7652 CNRS/ENSTA/École Polytechnique
3. Université Paris-Saclay
4. 91128 Palaiseau Cedex
5. France
Abstract
Reductive amination of aldehydes or ketones with suitable dihalogenated bicyclic aminocyclopropanes gives functionalised ring-expanded products in a single step.
Funder
Agence Nationale de la Recherche
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2017/OB/C7OB01238A
Reference57 articles.
1. The Formal [3+2+1] Cyclisation of Cyclopropylamines with Carboxylic Anhydrides: A Quick Access to Polysubstituted 2,3,3a,4-Tetrahydro6(5H)-indolone Ring Systems
2. The Intramolecular Aromatic Electrophilic Substitution of Aminocyclopropanes Prepared by the Kulinkovich-de Meijere Reaction
3. Aminocyclopropanes as precursors of endoperoxides with antimalarial activity
4. Synthesis of Polycyclic Aminocyclobutane Systems by the Rearrangement ofN-(ortho-Vinylphenyl) 2-Azabicyclo[3.1.0]hexane Derivatives
5. Gem-Dihalocyclopropanes in organic synthesis
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