Literature DB >> 14750802

Characteristics of the two frontier orbital interactions in the Diels-Alder cycloaddition.

Claude Spino1, Hadi Rezaei, Yves L Dory.   

Abstract

Two electron-deficient dienes were reacted with a series of twelve electron-poor and electron-rich dienophiles to give, in some cases, the corresponding Diels-Alder adducts. Clear differences in the roles played by the two frontier orbital interactions emerged. It was demonstrated that in the case of normal Diels-Alder cycloadditions, the FMO theory could predict the relative reactivities between dienophiles, while in the case of inverse-electron demand Diels-Alder reactions, it could not. It was shown that the dissymmetry in electron-rich dienophiles increases their reactivities.

Entities:  

Year:  2004        PMID: 14750802     DOI: 10.1021/jo0353740

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

Review 1.  Density functional theory studies of the antioxidants-a review.

Authors:  Samira Mahmoudi; Mehrdad Mohammadpour Dehkordi; Mohammad Hossein Asgarshamsi
Journal:  J Mol Model       Date:  2021-08-31       Impact factor: 1.810

2.  Genome-Mined Diels-Alderase Catalyzes Formation of the cis-Octahydrodecalins of Varicidin A and B.

Authors:  Dan Tan; Cooper S Jamieson; Masao Ohashi; Man-Cheng Tang; K N Houk; Yi Tang
Journal:  J Am Chem Soc       Date:  2019-01-08       Impact factor: 15.419

3.  A molecular electron density theory study of the participation of tetrazines in aza-Diels-Alder reactions.

Authors:  Luis R Domingo; Mar Ríos-Gutiérrez; Patricia Pérez
Journal:  RSC Adv       Date:  2020-04-21       Impact factor: 4.036

  3 in total

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