Iodine-catalyzed synthesis of benzoxazoles using catechols, ammonium acetate, and alkenes/alkynes/ketones via C-C and C-O bond cleavage

被引：4
|
作者：
Aboonajmi, Jasem [1 ]
Panahi, Farhad [1 ]
Hosseini, Mina Aali [1 ]
Aberi, Mahdi [2 ]
Sharghi, Hashem [1 ]
机构：
[1] Shiraz Univ, Coll Sci, Dept Chem, Shiraz 71454, Iran
[2] Tech & Vocat Univ TVU, Dept Chem & Mat Engn, Shiraz Branch, Fac Shahid Rajaee, Shiraz, Iran
来源：
RSC ADVANCES | 2022年 / 12卷 / 32期
关键词：
EFFICIENT CATALYST; ELEMENTAL SULFUR; OXIDATIVE SYNTHESIS; AMINES; DERIVATIVES; 2-PYRIDINYLBENZOXAZOLE; BENZIMIDAZOLES; ACETOPHENONES; HYDRATION; ANILINES;
D O I：
10.1039/d2ra03340b
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
An efficient metal-free synthesis strategy of benzoxazoles was developed via coupling catechols, ammonium acetate, and alkenes/alkynes/ketones. The developed methodology represents an operationally simple, one-pot and large-scale procedure for the preparation of benzoxazole derivatives using molecular iodine as the catalyst.
引用
收藏
页码：20968 / 20972
页数：5
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