TY  - JOUR
ID  - pittir20452
UR  - http://d-scholarship-dev.library.pitt.edu/20452/
IS  - 10
A1  - Du, W
A1  - Curran, DP
Y1  - 2003/05/15/
N2  - (Matrix presented) Tandem radical cyclizations of suitably substituted N-aryl thiocarbamates, thioamides, and thioureas are induced by exposure to tris(trimethylsilyl)-silane (TTMSH) and UV light and provide furoquinolines, isofuroquinolines, cyclopentaquinolines, indoloquinolines, and related ring systems. The intermediacy of an ?-thioalkylamino radical, which is the synthetic equivalent of an imidoyl radical, is invoked.
JF  - Organic Letters
VL  - 5
SN  - 1523-7060
TI  - Synthesis of carbocyclic and heterocyclic fused quinolines by cascade radical annulations of unsaturated N-aryl thiocarbamates, thioamides, and thioureas
SP  - 1765 
AV  - public
EP  -  1768
ER  -