Carbonylative synthesis of heterocycles involving diverse CO surrogates

被引:102
作者
Chen, Zhengkai [1 ]
Wang, Le-Cheng [1 ]
Wu, Xiao-Feng [1 ,2 ]
机构
[1] Zhejiang Sci Tech Univ, Dept Chem, Hangzhou 310018, Peoples R China
[2] Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany
基金
中国国家自然科学基金;
关键词
PALLADIUM-CATALYZED SYNTHESIS; DIRECT AEROBIC CARBONYLATION; CARBON-MONOXIDE SOURCE; TRANSITION-METAL-FREE; FORMIC-ACID; MOLYBDENUM HEXACARBONYL; BOND ACTIVATION; OXALIC-ACID; MEDIATED CARBONYLATION; SYNERGISTIC CATALYSIS;
D O I
10.1039/d0cc01504k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recent advances in the carbonylative synthesis of heterocycles by using diverse CO surrogates as sources of CO are summarized and discussed. The merger of carbonylative transformations involving CO surrogates with heterocyclic compound syntheses provides a powerful and promising tool for the construction of a series of carbonyl-containing heterocyclic compounds. In contrast to toxic and flammable gaseous carbon monoxide, most of the CO surrogates are readily available, bench-stable, harmless and easy to handle. This feature article will mainly focus on heterocycle syntheses involving CO surrogates, including formic acid, formates, molybdenum hexacarbonyl, etc.
引用
收藏
页码:6016 / 6030
页数:15
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