A DFT study of the mechanism and selectivities of the [3 + 2] cycloaddition reaction between 3-(benzylideneamino)oxindole and trans -β-nitrostyrene-Reference-Cited by-同舟云学术

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A DFT study of the mechanism and selectivities of the [3 + 2] cycloaddition reaction between 3-(benzylideneamino)oxindole and trans -β-nitrostyrene

Published:2016-09-09 Issue:6 Volume:30 Page:e3637
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Sobhi Chafia¹²,Khorief Nacereddine Abdelmalek²,Djerourou Abdelhafid²,Ríos- Gutiérrez Mar³,Domingo Luis R.³

Affiliation:

1. Department of Petrochemistry and Process Engineering, Faculty of Technology; University 20 Aout 1955 Skikda, BP 26, 21000; Skikda Algeria

2. Synthesis and Biocatalysis Organic Laboratory, Chemistry Department, Faculty of Sciences; Badji Mokhtar University, PB 12, 23000; Annaba Algeria

3. Department of Organic Chemistry; University of Valencia; Valencia Spain

Funder

European Social Fund

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference63 articles.

1. Prototropic routes to 1,3- and 1,5-dipoles, and 1,2-ylides: applications to the synthesis of heterocyclic compounds

2. A New Synthesis of 3,5-Diaryl-pyrrole-2-carboxylic Acids and Esters

3. 1,3-dipolar cycloaddition approach towards the stereoselective preparation of Aza-cephalotaxine skeleton

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