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Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
Published on: November 21, 2017
Ortho-Hydroxylative ipso-Cyclization of N-arylpropiolamide
Yu-Chao Wang1, Jin-Biao Liu1, Hongwei Zhou2
1School of Metallurgical and Chemical Engineering , Jiangxi University of Science and Technology , 86 Hongqi Road , Ganzhou 341000 , China.
Abstract:
A facile protocol for the tunable synthesis of 10-hydroxy-1-azaspiro[4.5]deca-3,6,8-trien-2-ones and benzo[b]pyrrolo[2,1-c][1,4]oxazin-3-ones is described. A tunable synthesis has been realized by the use of ZnBr2/oxone and tetra-n-butylammonium bromide (TBAB)/oxone. The reaction proceeds smoothly with high efficiency and a broad substrate scope. Mechanistic studies indicate that an N-protecting group-assisted ortho-trapping reaction is involved. In the transformation, the reaction undergoes α-addition, ipso-cyclization, and ortho-trapping of the resulting spirocyclic species.
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