Recent Developments in Copper-Catalyzed Annulations for Synthesis of Spirooxindoles

被引:0
作者
Feng, Jinzan [1 ]
Wang, Yue [1 ]
Li, Er-Qing [2 ]
Loh, Teck-Peng [1 ,3 ]
机构
[1] Henan Univ Technol, Coll Adv Interdisciplinary Sci & Technol CAIST, Zhengzhou 450001, Peoples R China
[2] Zhengzhou Univ, Coll Chem, Zhengzhou 450001, Peoples R China
[3] Nanyang Technol Univ, Sch Chem Chem Engn & Biotechnol, Singapore 637371, Singapore
基金
中国国家自然科学基金;
关键词
copper catalysis; intramolecular cyclization; intermolecular cyclization; synthetic methods; spirooxindoles; ONE-POT; ENANTIOSELECTIVE SYNTHESIS; LINKED 1,2,3-TRIAZOLES; C-H; DERIVATIVES; OXINDOLES; EFFICIENT; METAL; CYCLOADDITION; BIOSYNTHESIS;
D O I
10.1002/tcr.202400126
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Spirooxindoles represent a special scaffold for pharmaceuticals and natural products, and significant advancements have been achieved in their synthesis in recent years. Among these, transition metal catalysis, particularly copper catalysis, has emerged as an efficient and reliable method for the synthesis of spirooxindoles. Based on different reaction types, two distinct substrate types have been summarized and classified by us for constructing spirooxindole scaffolds via intramolecular and intermolecular annulations. This review outlines the latest advancements in copper-catalyzed cyclization reactions for synthesizing spirooxindoles and provides detailed insights into the types of annulation reactions and their possible reaction mechanisms. This review outlines the latest advancements in copper-catalyzed cyclization reactions for synthesizing spirooxindoles and provides detailed insights into the types of annulation reactions and their possible reaction mechanisms. image
引用
收藏
页数:18
相关论文
共 73 条
[1]  
[Anonymous], 2019, ANGEW CHEM INT EDIT, V58, P12190
[2]  
[Anonymous], 2021, ANGEW CHEM INT EDIT, V60, P3268
[3]  
[Anonymous], 2017, ANGEW CHEM INT EDIT, V56, P9577
[4]  
[Anonymous], 2015, ANGEW CHEM INT EDIT, V54, P1595
[5]  
[Anonymous], 2018, ANGEW CHEM INT EDIT, V57, P16852
[6]   Highly enantioselective synthesis and cellular evaluation of spirooxindoles inspired by natural products [J].
Antonchick, Andrey P. ;
Gerding-Reimers, Claas ;
Catarinella, Mario ;
Schuermann, Markus ;
Preut, Hans ;
Ziegler, Slava ;
Rauh, Daniel ;
Waldmann, Herbert .
NATURE CHEMISTRY, 2010, 2 (09) :735-740
[7]  
Arai T., 2015, Angew. Chem. Int. Ed, V127, P1615
[8]   Novel spirooxindole-pyrrolidine compounds: Synthesis, anticancer and molecular docking studies [J].
Arun, Y. ;
Saranraj, K. ;
Balachandran, C. ;
Perumal, P. T. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 74 :50-64
[9]   Lewis base-catalyzed synthesis of highly functionalized spirooxindole-pyranopyrazoles and their in vitro anticancer studies [J].
Asif, Mohd ;
Aqil, Farrukh ;
Alasmary, Fatmah Ali ;
Almalki, Amani Salem ;
Khan, Abdul Rahman ;
Nasibullah, Malik .
MEDICINAL CHEMISTRY RESEARCH, 2023, 32 (05) :1001-1015
[10]   Isatin-based three-component synthesis of new spirooxindoles using magnetic nano-sized copper ferrite [J].
Baghernejad, Mojtaba ;
Khodabakhshi, Saeed ;
Tajik, Sanaz .
NEW JOURNAL OF CHEMISTRY, 2016, 40 (03) :2704-2709