Literature DB >> 12020165

Thermal [1,3] carbon sigmatropic rearrangements of vinylcyclobutanes.

Phyllis A Leber1, John E Baldwin.   

Abstract

Stereochemical, kinetic, and theory-based studies of the [1,3] carbon sigmatropic rearrangements of bicyclo[2.1.1]hex-2-enes, bicyclo[3.2.0]hept-2-enes, and monocyclic vinylcyclobutanes support the judgment that such reactions involve transient diradical structures traversing relatively flat potential energy surfaces.

Entities:  

Year:  2002        PMID: 12020165     DOI: 10.1021/ar010100p

Source DB:  PubMed          Journal:  Acc Chem Res        ISSN: 0001-4842            Impact factor:   22.384


  4 in total

1.  Syntheses of Cyclic Guanidine-Containing Natural Products.

Authors:  Yuyong Ma; Saptarshi De; Chuo Chen
Journal:  Tetrahedron       Date:  2015-02-25       Impact factor: 2.457

2.  An approach for the synthesis of nakamuric acid.

Authors:  Xiaolei Wang; Chuo Chen
Journal:  Tetrahedron       Date:  2015-06-03       Impact factor: 2.457

3.  Alkoxide-induced ring opening of bicyclic 2-vinylcyclobutanones: A convenient synthesis of 2-vinyl-substituted 3-cycloalkene-1-carboxylic acid esters.

Authors:  Xiufang Ji; Zhiming Li; Quanrui Wang; Andreas Goeke
Journal:  Beilstein J Org Chem       Date:  2012-04-26       Impact factor: 2.883

4.  1,3-Alkyl Transposition in Allylic Alcohols Enabled by Proton-Coupled Electron Transfer.

Authors:  Kuo Zhao; Gesa Seidler; Robert R Knowles
Journal:  Angew Chem Int Ed Engl       Date:  2021-08-03       Impact factor: 16.823

  4 in total

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