Literature DB >> 24702158

Exploring the anionic reactivity of ynimines, useful precursors of metalated ketenimines.

Anouar Laouiti1, François Couty, Jérome Marrot, Taoufik Boubaker, Mohamed M Rammah, Mohamed B Rammah, Gwilherm Evano.   

Abstract

Insights into the reactivity of ynimines under anionic conditions are reported. They were shown to be excellent precursors of metalated ketenimines, which can be generated in situ by the reaction of ynimines with organolithium reagents or strong bases. The metalated ketenimines can then be trapped with various electrophiles and, depending on their substitution pattern, afford original and divergent entries to various building blocks.

Entities:  

Year:  2014        PMID: 24702158     DOI: 10.1021/ol500749h

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


  1 in total

1.  Harnessing the Electrophilicity of Keteniminium Ions: A Simple and Straightforward Entry to Tetrahydropyridines and Piperidines from Ynamides.

Authors:  Morgan Lecomte; Gwilherm Evano
Journal:  Angew Chem Int Ed Engl       Date:  2016-03-02       Impact factor: 15.336

  1 in total

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