I2/FeCl3 Promoted Cascade Reaction of 4-Quinazolinone, Pyridine, and Chalcone for the Synthesis of Indolizines

被引:1
作者
Meena, Mahesh [1 ]
Malviya, Bhanwar K. [1 ]
Singh, Karandeep [1 ]
Yadav, Priyanka [2 ]
Naharwal, Pankaj [1 ]
Kumari, Neetu [1 ]
Verma, Ved Prakash [2 ]
Yadav, Dinesh K. [1 ]
Sharma, Siddharth [1 ]
机构
[1] Mohanlal Sukhadia Univ, Dept Chem, Udaipur 313001, Rajasthan, India
[2] Banasthali Univ, Dept Chem, Newai Jodhpuriya Rd, Vanasthali, India
关键词
Chalcone; Cycloaddition; Indolizines; Quinazolinone; Zwitterions; DERIVATIVES; INHIBITORS; POTENT; FLUORESCENCE;
D O I
10.1002/slct.202201378
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The indolizines nucleus is an important element of many synthetic molecules with significant biological activity. An efficient methodology for the synthesis of a variety of indolizines from quinazolinone, pyridine, and chalcone via I-2/FeCl3 has been described. The reaction was promoted through Zwitterion formation/cyclization/aromatization sequence, affording the desired products in moderate to very good yields. This approach is a highly efficient and convenient way to get derivatives of indolizines from readily accessible substrate under relatively mild reaction conditions.
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页数:6
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