Ring opening of 2-phenylazetidines with allylsilanes
2006
Abstract N-Activated 2-phenylazetidines were opened regioselectively at the benzylic carbon with various allylsilanes or propargylsilane in the presence of BF 3 ·Et 2 O, providing amino olefins, precursors of biomolecules such as phenyl-homo-kainoids.
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