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.

Bibliográfalaš dieđut
Váldodahkkit: Smith, M, Lamb, A, Davey, P, Driver, R, Thompson, A
Materiálatiipa: Journal article
Almmustuhtton: American Chemical Society 2016
Govvádus
Čoahkkáigeassu: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.