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Synthesis of ortho-Phenolic Sulfilimines via an Intermolecular Sulfur Atom Transfer Cascade Reaction.
Xiong, Feng; Zuo, Yingying; Song, Yinan; Zhang, Linxing; Zhang, Xinhao; Xu, Shaojian; Ren, Yan.
Affiliation
  • Xiong F; School of Life Sciences, Nanjing University, Nanjing 210093, China.
  • Zuo Y; Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China.
  • Song Y; State Key Laboratory of Chemical Oncogenomics, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Zhang L; Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China.
  • Zhang X; State Key Laboratory of Chemical Oncogenomics, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Xu S; State Key Laboratory of Chemical Oncogenomics, Peking University Shenzhen Graduate School, Shenzhen 518055, China.
  • Ren Y; Hygiene Sector, Joint Laboratory for Infectious Disease Prevention and Control, Longhua District Center for Disease Control and Prevention, Shenzhen 518109, China.
Org Lett ; 22(10): 3799-3803, 2020 05 15.
Article in En | MEDLINE | ID: mdl-32337987
ABSTRACT
To expand the toolbox for the synthesis of ortho-phenolic sulfilimines, sigmatropic rearrangements were introduced to the field of sulfilimine chemistry. Herein we report a N-H sulfenylation/[2,3]-sigmatropic rearrangement cascade reaction. This mild reaction enables commercially available thiols to serve as the sulfenylation reagent and generates water as the sole byproduct. Moreover, the reaction has a wide substrate scope and can be conducted on a gram scale with excellent reaction efficiency.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2020 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2020 Document type: Article Affiliation country: China