Sharma Shweta, Kumar Mukesh, Vishwakarma Ram A, Verma Mahendra K, Singh Parvinder Pal
Medicinal Chemistry Division , Academy of Scientific and Innovative Research, CSIR-Indian Institute of Integrative Medicine , Canal Road , Jammu 180001 , India.
Analytical Chemistry Division , CSIR-Indian Institute of Integrative Medicine , Canal Road , Jammu 180001 , India.
J Org Chem. 2018 Oct 19;83(20):12420-12431. doi: 10.1021/acs.joc.8b01475. Epub 2018 Oct 9.
Herein, we report an original one-step, simple, room-temperature, regioselective Minisci reaction for the acylation of electron-deficient heteroarenes with alkynes. The method has broad functional group compatibility and gives exclusively monoacylated products in good to excellent yields. The mechanistic pathway was analyzed based on a series of experiments confirming the involvement of a radical pathway. The O-labeling experiment suggested that water is a source of oxygen in the acylated product, and head space GC-MS experiment shows the C-C cleavage occurs via release as CO.
在此,我们报道了一种新颖的一步法、简单、室温下用于缺电子杂芳烃与炔烃酰化反应的区域选择性Minisci反应。该方法具有广泛的官能团兼容性,能以良好至优异的产率专一性地得到单酰化产物。基于一系列证实自由基途径参与的实验对反应机理进行了分析。氧标记实验表明水是酰化产物中氧的来源,顶空气相色谱-质谱实验表明碳-碳键断裂是通过释放一氧化碳发生的。