Literature DB >> 25965074

Palladium-catalyzed C-H ethoxycarbonyldifluoromethylation of electron-rich heteroarenes.

Changdong Shao1, Guangfa Shi1, Yanghui Zhang1, Shulei Pan1, Xiaohong Guan2.   

Abstract

The first Pd-catalyzed C-H ethoxycarbonyldifluoromethylation with BrCF2CO2Et has been developed. The use of a bidentate phosphine ligand (Xantphos) is critical for the reaction to occur. A variety of electron-rich heteroarenes, including indoles, furans, thiophenes, and pyrroles, can be ethoxycarbonyldifluoromethylated in moderate to excellent yields. The reactions take place at the C-H bonds adjacent to the heteroatoms with high regioselectivity. This method provides a new protocol for the introduction of difuoroalkyl groups into electron-rich heteroarenes.

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Year:  2015        PMID: 25965074     DOI: 10.1021/acs.orglett.5b01024

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


  6 in total

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6.  2-Alkylation of 3-Alkyindoles With Unactivated Alkenes.

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  6 in total

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