A computational investigation of the selectivity and mechanism of the Lewis acid catalyzed oxa‐Diels–Alder cycloaddition of substituted diene with benzaldehyde-Reference-Cited by-同舟云学术

A computational investigation of the selectivity and mechanism of the Lewis acid catalyzed oxa‐Diels–Alder cycloaddition of substituted diene with benzaldehyde

Published:2021-04-30 Issue:18 Volume:42 Page:1296-1311
ISSN:0192-8651
Container-title:Journal of Computational Chemistry
language:en
Short-container-title:J Comput Chem

Author:

Khorief Nacereddine Abdelmalek¹^ORCID,Merzoud Lynda²^ORCID,Morell Christophe²^ORCID,Chermette Henry²^ORCID

Affiliation:

1. Laboratory of Physical Chemistry and Biology of Materials, Department of Physics and Chemistry, Higher Normal School of Technological Education‐Skikda, City of Boucetta Brothers, Azzaba Skikda Algeria

2. Institut des Sciences Analytiques Université de Lyon, CNRS, Université Claude Bernard Lyon 1 Villeurbanne Cedex France

Publisher

Wiley

Subject

Computational Mathematics,General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcc.26547

Reference71 articles.

1. Asymmetric hetero-Diels–Alder reactions of carbonyl compounds

2. Catalytic Asymmetric Hetero-Diels–Alder Reactions of Carbonyl Compounds and Imines

3. Hetero-Diels-Alder reaction in highly functionalized natural product synthesis

4. The Synthesis of Natural Heterocyclic Products by Hetero Diels-Alder Cycloaddition Reactions

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