Literature DB >> 28966404

Competitive, substrate-dependent reductive debromination/dehydrobromination of 1,2-dibromides with triethylamine.

Kristen M McGraw1, Greggory T Kent1, Joseph R Gonzalez1, Ihsan Erden1, Weiming Wu1.   

Abstract

The interaction of various 1,2-dibromides with NEt3 under various conditions (THF and DMF, respectively) at different temperatures was investigated. Our results from these reactions show that substrate dependent dehydrobrominations compete with reductive debrominations. A comprehensive discussion of these competitive pathways is offered.

Entities:  

Keywords:  Basicity; Debromination; Dehydrobromination; E1cB; α-CH acidity

Year:  2017        PMID: 28966404      PMCID: PMC5619868          DOI: 10.1016/j.tetlet.2017.04.024

Source DB:  PubMed          Journal:  Tetrahedron Lett        ISSN: 0040-4039            Impact factor:   2.415


  1 in total

1.  Formation of five- and seven-membered rings enabled by the triisopropylsilyl auxiliary group.

Authors:  Dmitry L Usanov; Hisashi Yamamoto
Journal:  Org Lett       Date:  2011-12-16       Impact factor: 6.005

  1 in total
  1 in total

1.  cis-β-Bromostyrene derivatives from cinnamic acids via a tandem substitutive bromination-decarboxylation sequence.

Authors:  Khanh G Tang; Greggory T Kent; Ihsan Erden; Weiming Wu
Journal:  Tetrahedron Lett       Date:  2017-08-31       Impact factor: 2.415

  1 in total

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