Synthesis of 3,3-dimethyl-2-phenyl-3H-pyrrole from Isopropyl Phenyl Ketoxime and Acetylene: A Side Formation of 4,4-dimethyl-5-phenyl-1-vinyl-2-pyrrolidinone as Clue to the Reaction Mechanism-Reference-Cited by-同舟云学术

Synthesis of 3,3-dimethyl-2-phenyl-3H-pyrrole from Isopropyl Phenyl Ketoxime and Acetylene: A Side Formation of 4,4-dimethyl-5-phenyl-1-vinyl-2-pyrrolidinone as Clue to the Reaction Mechanism

Published:2014-03 Issue:2 Volume:24 Page:100-101
ISSN:0959-9436
Container-title:Mendeleev Communications
language:en
Short-container-title:Mendeleev Communications

Author:

Shabalin Dmitrii A.,Glotova Tatyana E.,Schmidt Elena Yu.,Ushakov Igor A.,Mikhaleva Al’bina I.,Trofimov Boris A.

Publisher

Elsevier BV

Subject

General Chemistry

Reference18 articles.

1. in Advances in Heterocyclic Chemistry, Academic Press;Katritzky;New York,1982

2. in Pyrroles, Part 1, J. Wiley & Sons;Sammes;New York,1990

3. Diene autocondensation of 3,3-dimethyl-2-phenyl- and 3,3-dimethyl-2-(2-thienyl)-3H-pyrroles

4. Diels–Alder Reactions of 2-(Isoquinolin-1-yl)-5-phenyl-3H-pyrrole-3-carboxylic Esters with N-Methyl- and N-Phenyl-maleimides†

5. Osmium(II)-, Rhenium(I)-, and Tungsten(0)-Promoted Dipolar Cycloaddition Reactions with Pyrroles: Exploiting the Azomethine Ylide Character of This Heterocycle

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