relation: http://d-scholarship-dev.library.pitt.edu/20452/
title: Synthesis of carbocyclic and heterocyclic fused quinolines by cascade radical annulations of unsaturated N-aryl thiocarbamates, thioamides, and thioureas
creator: Du, W
creator: Curran, DP
description: (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 α-thioalkylamino radical, which is the synthetic equivalent of an imidoyl radical, is invoked.
date: 2003-05-15
type: Article
type: PeerReviewed
format: text/plain
language: en
rights: attached
identifier: http://d-scholarship-dev.library.pitt.edu/20452/1/licence.txt
identifier:   Du, W and Curran, DP  (2003) Synthesis of carbocyclic and heterocyclic fused quinolines by cascade radical annulations of unsaturated N-aryl thiocarbamates, thioamides, and thioureas.  Organic Letters, 5 (10).  1765 - 1768.  ISSN 1523-7060     
relation: 10.1021/ol0344319