Literature DB >> 19675915

Understanding the mechanism of polar Diels-Alder reactions.

Luis R Domingo1, José A Sáez.   

Abstract

A good correlation between the activation energy and the polar character of Diels-Alder reactions measured as the charge transfer at the transition state structure has been found. This electronic parameter controls the reaction rate to an even greater extent than other recognized structural features. The proposed polar mechanism, which is characterized by the electrophilic/nucleophilic interactions at the transition state structure, can be easily predicted by analyzing the electrophilicity/nucleophilicity indices defined within the conceptual density functional theory. Due to the significance of the polarity of the reaction, Diels-Alder reactions should be classified as non-polar (N), polar (P), and ionic (I).

Year:  2009        PMID: 19675915     DOI: 10.1039/b909611f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  44 in total

1.  Why are rhodanines less efficient reagents in Diels-Alder reactions than isorhodanines? A quantum chemical study.

Authors:  Waldemar Tejchman; Michal Michalski; Krzysztof K Zborowski; Slawomir Berski
Journal:  J Mol Model       Date:  2019-06-14       Impact factor: 1.810

2.  Understanding the role of the trifluoromethyl group in reactivity and regioselectivity in [3+2] cycloaddition reactions of enol acetates with nitrones. A DFT study.

Authors:  Hatem Layeb; Abdelmalek Khorief Nacereddine; Abdelhafid Djerourou; Mar Ríos-Gutiérrez; Luis R Domingo
Journal:  J Mol Model       Date:  2015-04-08       Impact factor: 1.810

3.  The Intramolecular Diels-Alder Reaction of Tryptamine-Derived Zincke Aldehydes Is a Stepwise Process.

Authors:  Hung V Pham; David B C Martin; Christopher D Vanderwal; K N Houk
Journal:  Chem Sci       Date:  2012-02-02       Impact factor: 9.825

4.  Experimental and theoretical studies of Diels-Alder reaction between methyl (Z)-2-nitro-3-(4-nitrophenyl)-2-propenoate and cyclopentadiene.

Authors:  Radomir Jasiński; Magdalena Kwiatkowska; Valentin Sharnin; Andrzej Barański
Journal:  Monatsh Chem       Date:  2013-01-09       Impact factor: 1.451

5.  Kinetics of the [4+2] cycloaddition of cyclopentadiene with (E)-2-aryl-1-cyano-1-nitroethenes.

Authors:  Radomir Jasiński; Magdalena Kwiatkowska; Andrzej Barański
Journal:  Monatsh Chem       Date:  2012-03-02       Impact factor: 1.451

6.  An integrated molecular modeling protocol for drug screening based on conceptual density functional theory and chemoinformatics for the study of marine cyclopeptides.

Authors:  Norma Flores-Holguín; Juan Frau; Daniel Glossman-Mitnik
Journal:  J Mol Model       Date:  2021-10-08       Impact factor: 1.810

7.  An insight into reactivity and bioactivity properties of quorum sensing peptides against PDE10A: a computational peptidology approach.

Authors:  Bhargav Shreevatsa; Chandan Dharmashekara; Anisha S Jain; Raghavendra Amachawadi; Asad Syed; Chandan Shivamallu; Shiva Prasad Kollur; Juan Frau; Norma Flores-Holguín; Daniel Glossman-Mitnik; Raghu Ram Achar
Journal:  J Mol Model       Date:  2022-07-05       Impact factor: 2.172

8.  Decreasing Distortion Energies without Strain: Diazo-Selective 1,3-Dipolar Cycloadditions.

Authors:  Brian Gold; Matthew R Aronoff; Ronald T Raines
Journal:  J Org Chem       Date:  2016-07-07       Impact factor: 4.354

9.  Understanding the high reactivity of triazolinediones in Diels-Alder reactions. A DFT study.

Authors:  María A Fernández-Herrera; Claudia Zavala-Oseguera; José Luis Cabellos; Jesús Sandoval-Ramírez; Luis R Domingo; Gabriel Merino
Journal:  J Mol Model       Date:  2014-04-02       Impact factor: 1.810

10.  Density Functional Theory Guide for an Allyl Monomer Polymerization Mechanism: Photoinduced Radical-Mediated [3 + 2] Cyclization.

Authors:  Xiaotian Zhao; Wanqiu Huang; Shibo Lin; Xi Chen; Xirui Guo; Dehong Zou; Guodong Ye
Journal:  ACS Omega       Date:  2021-06-08
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