Synthetic routes to access dicarbonylated aryls and heteroaryls

被引:4
作者
Acharya, Swadhin Swaraj [1 ]
Parida, Bibhuti Bhusan [1 ]
机构
[1] Berhampur Univ, PG Dept Chem, Organ Synth Lab, Bhanja 760007, Odisha, India
关键词
METHYL KETONES; C-H; 1,2-DICARBONYL COMPOUNDS; MULTICOMPONENT SYNTHESIS; ANTICANCER AGENTS; INDOLES; DERIVATIVES; BENZIL; GREEN; IMIDAZOHETEROCYCLES;
D O I
10.1039/d4ob01278j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
1,2-Dicarbonyl compounds are privileged functionalities found in natural products, pharmaceuticals, bioactive molecules, and food items, and are important precursors in catalysis, asymmetric synthesis, polymer chemistry and synthesizing functionalized heterocycles. Herein, this comprehensive review focuses on various approaches for synthesizing 1,2-dicarbonylated aryls and heteroaryls in both intermolecular and intramolecular fashion, covering the dicarbonylation of indoles, imidazoheterocycles, indolizines, aminopyrazoles, pyrroloisoquinolines, coumarins, furan, anilines, phenols, anthranils, and benzil synthesis over the last decade (since 2015). Also, the present review highlights the scope and future perspectives of the approach. The regioselective 1,2-dicarbonylation of aryls and heteroaryls offers access to functionalized dicarbonylated aryls and heteroaryls, which opens access to pharmaceuticals and bioactive molecules with diverse synthetic utility.
引用
收藏
页码:8209 / 8248
页数:40
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