A novel approach to 1-aryl-2-(p-tolylazo)alkenes from alkyl aryl ketones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
1. Behaviour of Arylazo tert-Butyl Sulfides with Ketone Enolates. Competition between SRN1 α-arylation and Azocoupling Reactions.
2. α-arylation vs. α-arylhydrazonylation of alkyl aryl ketones with arylazo tert-butyl sulfides
3. Competitive Pathways in the Reaction between Aromatic Azosulfides and Enolates in DMSO
4. An easy access to 2-oxohydrazones via electrophilic α-p-tolylhydrazonylation of ketone enolates with tert-butyl p-tolylazo sulfide
5. Electrophilicα-p-tolylhydrazonylation of tert-butyl alkanoates and tertiary alkanamides with tert-butylp-tolylazo sulfide
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1. Fast, efficient and convenient method for the preparation of arylazo sulfides using aryl diazonium silica sulfates under mild and solvent-free conditions;Dyes and Pigments;2011-10
2. ChemInform Abstract: A Novel Approach to 1-Aryl-2-(p-tolylazo)alkenes from Alkyl Aryl Ketones.;ChemInform;2010-06-20
3. Synthesis of new cycloalkenyliden-pyrroles by domino reaction;Tetrahedron;2009-03
4. Azavinyl Azomethine Ylides from Thermal Ring Opening of α-Aziridinohydrazones: Unprecedented 1,5-Electrocyclization to Imidazoles;Organic Letters;2007-07-28
5. Straightforward Access to Pyrazines, Piperazinones, and Quinoxalines by Reactions of 1,2-Diaza-1,3-butadienes with 1,2-Diamines under Solution, Solvent-Free, or Solid-Phase Conditions;The Journal of Organic Chemistry;2006-06-30
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