media has emerged as a new facet of green chemistry. In this paper, a sulfone‐containing imidazolium‐based Brønsted acid ionic liquid was prepared and used as a recyclable acid catalyst. The ionic liquid catalyst enables the use of an industrially acceptable and environmentally benign solvent, butyl acetate, as the reaction medium. The ionic liquid/butyl acetate biphasic system was successfully utilized
Rhodium(III)-Catalyzed Amidation of Aryl Ketone<i>O</i>-Methyl Oximes with Isocyanates by CH Activation: Convergent Synthesis of 3-Methyleneisoindolin-1-ones
作者:Bing Zhou、Wei Hou、Yaxi Yang、Yuanchao Li
DOI:10.1002/chem.201204448
日期:2013.4.8
Going green! The rhodium(III)‐catalyzed annulation of arylketone O‐methyl oximes with isocyanates for the synthesis of 3‐methyleneisoindolin‐1‐ones is reported (see scheme). This reaction exhibits high regioselectivity, functional‐group tolerance, and broad substrate scope, without the use of additives or production of environmentally hazardous waste.
Copper-catalyzed direct synthesis of 3-methylene-2-arylisoindolin-1-ones with calcium carbide as a surrogate of gaseous acetylene
作者:Jianglong Wu、Yinfeng Ma、Yan Wang、Chenyu Wang、Hui Luo、Dianjun Li、Jinhui Yang
DOI:10.1039/d2gc03572c
日期:——
A novel strategy for the synthesis of 3-methylene-2-arylisoindolin-1-ones through Sonogashira cross-coupling/nucleophilic addition reactions using calcium carbide as a surrogate of gaseous acetylene, 2-bromo-N-(2-bromophenyl)benzamide substrates as starting materials, and copper as a catalyst was described. The salient features of this protocol are the use of a readily available and easy-to-handle