Literature DB >> 18165954

Superelectrophiles: charge-charge repulsive effects.

Douglas A Klumpp1.   

Abstract

Over the years, a significant number of di- and tricationic superelectrophiles have been studied. Many of these superelectrophiles exhibit charge-charge repulsive effects due to the interaction of the positive charges. Charge-charge repulsion can lead to novel molecular rearrangements, profoundly influence reactivities, and may significantly effect molecular structure.

Year:  2008        PMID: 18165954     DOI: 10.1002/chem.200701470

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

1.  Superacid-promoted synthesis of quinoline derivatives.

Authors:  Hein Vuong; Michael R Stentzel; Douglas A Klumpp
Journal:  Tetrahedron Lett       Date:  2020-01-14       Impact factor: 2.415

2.  Dicationic ring-opening reactions of trans-2-phenylcyclopropylamine·HCl: electrophilic cleavage of the distal (C2-C3) bond of cyclopropanes.

Authors:  Sten O Nilsson Lill; Rajasekhar Reddy Naredla; Matthew E Zielinski; Larecia Knoecer; Douglas A Klumpp
Journal:  J Org Chem       Date:  2013-08-26       Impact factor: 4.354

Review 3.  Superelectrophiles: Recent Advances.

Authors:  Douglas A Klumpp; Maksim V Anokhin
Journal:  Molecules       Date:  2020-07-19       Impact factor: 4.411

4.  Stereoselective gridization and polygridization with centrosymmetric molecular packing.

Authors:  Dongqing Lin; Ying Wei; Aizhong Peng; He Zhang; Chunxiao Zhong; Dan Lu; Hao Zhang; Xiangping Zheng; Lei Yang; Quanyou Feng; Linghai Xie; Wei Huang
Journal:  Nat Commun       Date:  2020-04-09       Impact factor: 14.919

  4 in total

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