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Autor: Hai-Jun, Tang, Yu-Feng, Zhang, Yi-Wen, Jiang, Chao, Feng
Rok vydání: 2018
Zdroj: Organic letters. 20(17)
ISSN: 1523-7052
Popis: An efficient [3 + 2] annulation of (2,2-difluorovinyl)-2-iodoarenes and internal alkynes was developed for the synthesis of 1-(trifluoromethyl)-1 H-indenes. The success of this strategy hinges upon a well-balanced process for the generation of two transient reactive species, specifically trifluoroethylsilver and alkenylpalladium intermediates, in the same molecule, as well as a smooth transmetalation step, which delicately joins together these two different metallic intermediates.
Databáze: OpenAIRE