Enantioselective synthesis of 4- and 6-azaindolines by a cation-directed cyclization

Functionalized 4- and 6-azaindolines are accessible with high levels of enantioselectivity by the cation-directed cyclization of aminopyridine-derived imines via phase-transfer catalysis. The extension of this methodology to diastereoselective cyclizations is also described.

Podrobná bibliografie
Hlavní autoři: Smith, M, Lamb, A, Davey, P, Driver, R, Thompson, A
Médium: Journal article
Vydáno: American Chemical Society 2016