Literature DB >> 32242553

Electrochemically generated N-iodoaminium species as key intermediates for selective methyl sulphonylimination of tertiary amines.

Binbin Huang1, Chao Yang, Jia Zhou, Wujiong Xia.   

Abstract

Reported herein is a straightforward protocol for approaching N-sulphonylamidines via an electricity-driven, iodine-mediated cross dehydrogenative condensation (CDC) between sulphonamides and tertiary amines, which features exclusive N-CH3 selectivity for the amine partners. Mechanistic studies indicate that an in situ generated N-iodoaminium species serves as the key intermediate.

Entities:  

Year:  2020        PMID: 32242553     DOI: 10.1039/c9cc09869k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  4 in total

1.  Catalyst-free one-pot, four-component approach for the synthesis of di- and tri-substituted N-sulfonyl formamidines.

Authors:  Ai-Ran Liu; Lei Zhang; Jiao Li; Abudureheman Wusiman
Journal:  RSC Adv       Date:  2021-04-27       Impact factor: 3.361

2.  Visible-light enabled room-temperature dealkylative imidation of secondary and tertiary amines promoted by aerobic ruthenium catalysis.

Authors:  Dong Yang; Jingqi Shi; Jiaming Chen; Xiaoqi Jia; Cuiying Shi; Lifang Ma; Ziyuan Li
Journal:  RSC Adv       Date:  2021-05-25       Impact factor: 4.036

3.  Rapid and efficient synthesis of formamidines in a catalyst-free and solvent-free system.

Authors:  Zitong Zhou; Yu Zhao; Donghua Zhou; Li Li; Hui Luo; Liao Cui; Weiguang Yang
Journal:  RSC Adv       Date:  2021-10-18       Impact factor: 4.036

4.  Selective N-Alkylation of Amines with DMC over Biogenic Cu-Zr Bimetallic Nanoparticles.

Authors:  Ashutosh Sharma; Khushboo Verma; Sandeep Kaushal; Rahul Badru
Journal:  ACS Omega       Date:  2021-06-07
  4 in total

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