Literature DB >> 27486792

Aryne Compatible Solvents are not Always Innocent.

Sung-Eun Suh1, David M Chenoweth1.   

Abstract

Arynes are important and versatile intermediates in a variety of transformations. Commonly used solvents for aryne chemistry include acetonitrile and dichloromethane. Although rarely reported, the reactive nature of aryne intermediates makes them prone to side reactions, which sometimes involve solvent participation. Acetonitrile and dichloromethane are not always innocent solvents and can participate in aryne-based reactions. These results are presented in the context of ongoing mechanistic investigations of the triple aryne-tetrazine reaction.

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Year:  2016        PMID: 27486792     DOI: 10.1021/acs.orglett.6b01977

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Intramolecular hydride transfer onto arynes: redox-neutral and transition metal-free C(sp3)-H functionalization of amines.

Authors:  Fahima I M Idiris; Cécile E Majesté; Gregory B Craven; Christopher R Jones
Journal:  Chem Sci       Date:  2018-02-08       Impact factor: 9.825

2.  The mechanism of the triple aryne-tetrazine reaction cascade: theory and experiment.

Authors:  Sung-Eun Suh; Shuming Chen; K N Houk; David M Chenoweth
Journal:  Chem Sci       Date:  2018-08-23       Impact factor: 9.825

3.  Exploring Possible Surrogates for Kobayashi's Aryne Precursors.

Authors:  Ana Carolina A Muraca; Cristiano Raminelli
Journal:  ACS Omega       Date:  2020-01-31
  3 in total

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