Recent Advances on Benzofuranones: Synthesis and Transformation via C-H Functionalization

被引:5
|
作者
Tang, Zhi [1 ,2 ]
Tong, Zhou [1 ]
Qiu, Renhua [1 ]
Yin, Shuang-Feng [1 ]
Kambe, Nobuaki [1 ,3 ]
机构
[1] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Minist Educ,Adv Catalyt Engn Res Ctr, Changsha 410082, Peoples R China
[2] Hainan Univ, Minist Educ Adv Mat Trop Isl Resources, Key Lab, Hainan Prov Key Lab Fine Chem, Haikou 570228, Hainan, Peoples R China
[3] Osaka Univ, Inst Sci & Ind Res, 8-1 Mihogaoka, Ibaraki, Osaka 5670047, Japan
来源
SYNTHESIS-STUTTGART | 2021年 / 53卷 / 18期
关键词
benzofuranone; C-H bond functionalization; transitionmetal catalysis; cross coupling; ENANTIOSELECTIVE MICHAEL ADDITION; CATALYZED CARBONYLATIVE SYNTHESIS; ASYMMETRIC ALLYLIC ALKYLATION; 3-SUBSTITUTED BENZOFURAN-2(3H)-ONES; 3-ARYL BENZOFURAN-2(3H)-ONES; SPIROCYCLIC BENZOFURANONES; FRIES REARRANGEMENT; MANDELIC-ACIDS; FORMIC-ACID; HOPEAHAINOL;
D O I
10.1055/a-1405-5761
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The benzofuranone structure is important in many fields, such as natural products, pharmaceuticals, building blocks, antioxidants, and dyes. The efficient synthesis and transformation of benzofuranones have attracted great attention in organic synthesis. They can be synthesized by the Friedel-Crafts reaction and intramolecular dehydration ring-closing and transition-metal-catalyzed reactions, among others. Their direct utilization in the preparation of other functional molecules further enhance their application. Due to their low pk, value and easy enolization, the transformation of benzofuranones via C(3)-H bond functionalization has been a hot issue since 2010. Herein, we highlight advances in the synthesis of benzofuranones and their transformation via C-H functionalization. Other transformations related to benzofuranones are also discussed.
引用
收藏
页码:3193 / 3210
页数:18
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