Literature DB >> 24091639

Cascade fluorofunctionalisation of 2,3-unsubstituted indoles by means of electrophilic fluorination.

Tuan Minh Nguyen1, Hung A Duong, Jean-Alexandre Richard, Charles William Johannes, Fu Pincheng, Danson Kwong Jia Ye, Eileen Lau Shuying.   

Abstract

Cascade fluorofunctionalisation of 2,3-unsubstituted indoles featuring the formation of C-C, C-F and C-O bonds via electrophilic fluorination using N-fluorobenzenesulfonimide is described. The use of an O-nucleophile tethered to the nitrogen of indoles enables the synthesis of polycyclic fluorinated indoline derivatives from simple precursors in 40-63% yields.

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Year:  2013        PMID: 24091639     DOI: 10.1039/c3cc46564k

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


  2 in total

1.  An intramolecular cascade cyclization of 2-aryl indoles: efficient methods for the construction of 2,3-functionalized indolines and 3-indolinones.

Authors:  Arun K Ghosh; Zhi-Hua Chen
Journal:  Org Biomol Chem       Date:  2014-05-01       Impact factor: 3.876

2.  Synthesis and biological evaluation of fluoro-substituted spiro-isoxazolines as potential anti-viral and anti-cancer agents.

Authors:  Prasanta Das; Sarah Boone; Dipanwita Mitra; Lindsay Turner; Ritesh Tandon; Drazen Raucher; Ashton T Hamme
Journal:  RSC Adv       Date:  2020-08-17       Impact factor: 4.036

  2 in total

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