Literature DB >> 28737408

Establishing the Trifluoromethylthio Radical Donating Abilities of Electrophilic SCF3-Transfer Reagents.

Man Li1, Biying Zhou1, Xiao-Song Xue1, Jin-Pei Cheng1,2.   

Abstract

The recent recognition of the novel application of a few traditional electrophilic trifluoromethylthiolating reagents as SCF3 radical sources offers a remarkable new opportunity for the development of radical trifluoromethylthiolation reactions. Herein, the first trifluoromethylthio radical donating ability (Tt•DA) scale of electrophilic SCF3-transfer reagents has been developed. This scale is based on Y-SCF3 bond dissociation energies, which were obtained by density functional calculations (M06-2X). Single electron transfer is revealed to exhibit a substantial Y-SCF3 bond-weakening effect, thus significantly facilitating the SCF3 radical (•SCF3) release. The results may aid in future novel radical SCF3-transfer reagent design and new reaction development.

Entities:  

Year:  2017        PMID: 28737408     DOI: 10.1021/acs.joc.7b01771

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  N-Trifluoromethylthiolated Sulfonimidamides and Sulfoximines: Anti-microbial, Anti-mycobacterial, and Cytotoxic Activity.

Authors:  Niranjan Thota; Parameshwar Makam; Kamal K Rajbongshi; Savania Nagiah; Naeem Sheik Abdul; Anil A Chuturgoon; Amit Kaushik; Gyanu Lamichhane; Anou M Somboro; Hendrik G Kruger; Thavendran Govender; Tricia Naicker; Per I Arvidsson
Journal:  ACS Med Chem Lett       Date:  2019-09-11       Impact factor: 4.345

2.  Catalyst-Free Decarbonylative Trifluoromethylthiolation Enabled by Electron Donor-Acceptor Complex Photoactivation.

Authors:  Alexander Lipp; Shorouk O Badir; Ryan Dykstra; Osvaldo Gutierrez; Gary A Molander
Journal:  Adv Synth Catal       Date:  2021-05-19       Impact factor: 5.981

  2 in total

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