The generation and reactivity of N-substituted, stabilised α,β:γ,δ-unsaturated azomethine ylides-Reference-Cited by-同舟云学术

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The generation and reactivity of N-substituted, stabilised α,β:γ,δ-unsaturated azomethine ylides

Published:2002-01 Issue:5 Volume:58 Page:989-995
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Nyerges Miklós,Arany Andrea,Fejes Imre,Groundwater Paul W,Zhang Weimin,Bendell David,Anderson Rosaleen J,Tőke László

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

1. 1,5-Dipolar cyclizations

2. 1,5,-Electrocyclizations—An Important Principle of Heterocyclic Chemistry

3. 1,7-Electrocyclisation of non-stabilised azomethine ylides

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1. Recent advances in 8π electrocyclization reactions;Chemical Communications;2023

2. Short Synthesis of Enantiopure trans-3-Arylpiperazine-2-carboxylic Acid Derivatives via Diaza-Cope Rearrangement;Organic Letters;2012-07-06

3. Electrocyclization reactions of vinyl, styryl, and butadienyl conjugated carbonyl/azomethine ylides;Tetrahedron;2010-08

4. ChemInform Abstract: The Generation and Reactivity of N-Substituted, Stabilized α,β:γ,δ-Unsaturated Azomethine Ylides.;ChemInform;2010-05-21

5. 3-Alkylsulfanyl-2-arylazo-3-(pyrrolidin-1-yl)-acrylonitriles as masked 1,3-dipoles;Tetrahedron;2009-09

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