Literature DB >> 27409978

Vicinal Diamination of Arenes with Domino Aryne Precursors.

Lu Li1, Dachuan Qiu1, Jiarong Shi1, Yang Li1.   

Abstract

Vicinal diamination of domino aryne precursors was achieved with sulfamides. The reaction proceeds through a two-aryne pathway, accepting two N-nucleophiles at the 1,2-positions of an arene ring. Symmetrical and unsymmetrical diaminobenzenes were readily obtained.

Entities:  

Year:  2016        PMID: 27409978     DOI: 10.1021/acs.orglett.6b01747

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


  3 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

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.