Cyclobutenones and Benzocyclobutenones: Versatile Synthons in Organic Synthesis

被引:110
作者
Chen, Peng-hao [1 ]
Dong, Guangbin [1 ,2 ]
机构
[1] Univ Texas Austin, Dept Chem, 100 East 24th St, Austin, TX 78712 USA
[2] Univ Chicago, Dept Chem, 5735 S Ellis Ave, Chicago, IL 60637 USA
关键词
cycloaddition; electrocyclic reactions; enones; homogeneous catalysis; strained molecules; C-C BOND; RH-CATALYZED CARBOACYLATION; SMALL-RING COMPOUNDS; HIGHLY-SUBSTITUTED AROMATICS; CARBON-CARBON BOND; REGIOSPECIFIC SYNTHESIS; THERMAL REARRANGEMENT; REGIOCONTROLLED CONSTRUCTION; STEREOCHEMICAL SELECTIVITIES; ELECTROCYCLIC REACTIONS;
D O I
10.1002/chem.201603382
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyclobutenones, four-membered ketones bearing an unsaturated carbon-carbon double bond, and their structural sibling benzocyclobutenones, possess unique reactivity. Owing to their inherent high ring strain, such structures readily undergo ring opening under a variety of conditions, including thermolysis, photolysis, and transition metal catalysis, to afford reactive intermediates that can be trapped with nucleophiles, dienophiles, and unsaturated bonds. Their electron-deficient enone moieties are good electrophiles for facile nucleophilic addition. Such properties render cyclobutenones versatile synthons, serving as excellent coupling partners in a vast array of synthetically valuable transformations.
引用
收藏
页码:18290 / 18315
页数:26
相关论文
共 143 条
[1]   A NOVEL SYNTHESIS OF BENZOCYCLOBUTENONES [J].
AIDHEN, IS ;
AHUJA, JR .
TETRAHEDRON LETTERS, 1992, 33 (37) :5431-5432
[2]   Pd-Catalyzed Intramolecular Acylation of Aryl Bromides via C-H Functionalization: A Highly Efficient Synthesis of Benzocyclobutenones [J].
Alvarez-Bercedo, Paula ;
Flores-Gaspar, Areli ;
Correa, Arkaitz ;
Martin, Ruben .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (02) :466-+
[3]  
[Anonymous], 2014, ANGEW CHEM, V126, P1922
[4]  
[Anonymous], 2019, ANGEW CHEM, V131, P7884
[5]  
[Anonymous], 1999, ANGEW CHEM, V111, P918
[6]  
[Anonymous], 2014, ANGEW CHEM, V126, P1700
[7]  
[Anonymous], 2015, ANGEW CHEM, V127, P9673
[8]  
[Anonymous], 2005, ANGEW CHEM, V117, P1247
[9]  
[Anonymous], 1969, ANGEW CHEM, V81, P33
[10]  
[Anonymous], 2011, ANGEW CHEM, V123, P2821