Literature DB >> 31329453

N-Alkynylthio Phthalimide: A Shelf-Stable Alkynylthio Transfer Reagent for the Synthesis of Alkynyl Thioethers.

Wen-Chao Gao1,2, Yu-Zhu Shang1, Hong-Hong Chang1, Xing Li1, Wen-Long Wei1, Xin-Zhang Yu3, Rong Zhou1.   

Abstract

A new kind of electrophilic alkynylthiolating reagent, called N-alkynylthio phthalimide, is designed and synthesized herein. This electrophilic sulfenylating reagent can be easily prepared in three steps from commercially available phthalimide and corresponding silver acetylide. Furthermore, the N-alkynylthio phthalimides are demonstrated to be efficient alkynylthio transfer reagents that can react with various C-nucleophiles, including β-ketoesters, aryl boronic acids, and Grignard reagents to afford a diverse range of alkynyl thioethers under mild conditions.

Entities:  

Year:  2019        PMID: 31329453     DOI: 10.1021/acs.orglett.9b02174

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


  2 in total

1.  The Three-Component Synthesis of 4-Sulfonyl-1,2,3-triazoles via a Sequential Aerobic Copper-Catalyzed Sulfonylation and Dimroth Cyclization.

Authors:  Max Van Hoof; Santhini Pulikkal Veettil; Wim Dehaen
Journal:  Molecules       Date:  2021-01-22       Impact factor: 4.411

2.  One-step synthesis of benzo[b]thiophenes by aryne reaction with alkynyl sulfides.

Authors:  Tsubasa Matsuzawa; Takamitsu Hosoya; Suguru Yoshida
Journal:  Chem Sci       Date:  2020-09-01       Impact factor: 9.825

  2 in total

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