Article ID Journal Published Year Pages File Type
4909325 Journal of Saudi Chemical Society 2017 8 Pages PDF
Abstract

The reaction of aryne with aza-Morita-Baylis-Hillman (aza-MBH) adducts has been studied. Aryne reacts with aza-MBH adducts through a cascade insertion-cyclization-ene reaction to produce 4-quinolones in 18-44% yields; meanwhile, aza-MBH adducts undergo N-insertion reaction with aryne to afford N-arylation products in 27-77% yields.

Related Topics
Physical Sciences and Engineering Chemical Engineering Chemical Engineering (General)
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