Literature DB >> 27304928

Diamination of Domino Aryne Precursor with Sulfonamides.

Dachuan Qiu1, Jia He1, Xiao Yue1, Jiarong Shi1, Yang Li1.   

Abstract

The reaction of a domino aryne precursor with sulfonamides efficiently afforded both 1,3-diaminobenzenes and trisubstituted 1,3-diaminobenzenes by simply varying the reaction conditions. Mechanistic study supports the sequential formation of two transient aryne intermediates involved in the reaction.

Entities:  

Year:  2016        PMID： 27304928     DOI： 10.1021/acs.orglett.6b01334

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


  4 in total

1.  Sulfonamide-Trapping Reactions of Thermally Generated Benzynes.

Authors:  Yuanxian Wang; Lianyou Zheng; Thomas R Hoye
Journal:  Org Lett       Date:  2018-11-05       Impact factor: 6.005

2.  One-Pot, Three-Aryne Cascade Strategy for Naphthalene Formation from 1,3-Diynes and 1,2-Benzdiyne Equivalents.

Authors:  Xiao Xiao; Thomas R Hoye
Journal:  J Am Chem Soc       Date:  2019-06-14       Impact factor: 15.419

3.  "Kobayashi Benzynes" as Hexadehydro-Diels-Alder Diynophiles.

Authors:  Sahil Arora; Thomas R Hoye
Journal:  Org Lett       Date:  2021-04-22       Impact factor: 6.005

4.  Synthesis of Aryl Triflones through the Trifluoromethanesulfonylation of Benzynes.

Authors:  Yuji Sumii; Yutaka Sugita; Etsuko Tokunaga; Norio Shibata
Journal:  ChemistryOpen       Date:  2018-02-27       Impact factor: 2.911
  4 in total

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