Abstract
(Figure Presented) Make it strained and fluorinated! A rhodium-catalyzed domino diazotization/ cyclopropenation reaction involving trifluoroethylamine hydrochloride and alkynes has been developed for the synthesis of trifluoromethyl cyclopropenes that can be easily functionalized to afford useful CF3- containing building blocks for drug discovery. © 2010 Wiley-VCH Verlag GmbH &. Co. KGaA, Weinheim.
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Morandi, B., & Carreira, E. M. (2010). Rhodium-catalyzed cyclopropenation of alkynes: Synthesis of trifluoromethyl-substituted cyclopropenes. Angewandte Chemie - International Edition, 49(25), 4294–4296. https://doi.org/10.1002/anie.201000787
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