Transformation of 5-acylated N -fluoroalkyl-1,2,3-triazoles to trifluoromethylated ring-fused isoquinolines, 1,3-oxazines, and 1,3-oxazin-6-ones via ketenimines.
Lukáš JaneckýBlanka KlepetářováPetr BeierPublished in: RSC advances (2024)
A one-pot multistep methodology leading to trifluoromethylated cyclopenta[ c ]isoquinolines, indeno[1,2- c ]isoquinolines, 6,6-difluoro-1,3-oxazines, or 1,3-oxazin-6-ones, based on the reaction of 5-acylated N -pentafluoroethyl-substituted 1,2,3-triazoles is presented. A thermal ring opening of the starting triazoles, followed by a 1,2-acyl shift formed reactive ketenimines which cyclized after a rearrangement in a substrate-specific manner to provide new trifluoromethylated heterocyclic products.
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