Unimolecular Fragment Coupling: A New Bond-Forming Methodology via the Deletion of Atom(s)

被引:13
作者
Shimazumi, Ryoma [1 ]
Tobisu, Mamoru [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Engn, Dept Appl Chem, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Inst Open & Transdisciplinary Res Initiat ICS OTRI, Innovat Catalysis Sci Div, Suita, Osaka 5650871, Japan
来源
JACS AU | 2024年 / 4卷 / 05期
基金
日本学术振兴会;
关键词
Unimolecular Fragment Coupling; TransitionMetal Catalysis; Decarboxylation; Decarbonylation; Deisocyanation; Deoxygenation; Skeletal Editing; C-C-BOND; CARBON-CARBON BONDS; NICKEL-CATALYZED DECARBONYLATION; ARYL KETONES; CONJUGATED YNONES; NATURAL-PRODUCTS; ACTIVATION; PALLADIUM; CLEAVAGE; RECOMBINATION;
D O I
10.1021/jacsau.3c00827
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Unimolecular fragment coupling (UFC) is defined as a reaction format, wherein atom(s) located in the middle of a molecule are extruded, and the remaining fragments are coupled. UFC is a potentially powerful strategy that is an alternative to transition-metal-catalyzed cross-coupling because the target chemical bond is formed in an intramolecular fashion, which is inherently beneficial for chemoselectivity and stereoselectivity issues. In this Perspective, we will present an overview of the recent advances in UFC reactions, which encompass those proceeding through the elimination of CO2, CO, SO2, isocyanates, N-2, or single atoms primarily via transition metal catalysis.
引用
收藏
页码:1676 / 1695
页数:20
相关论文
共 156 条
[1]   Transition-Metal-Catalyzed Direct Arylation of (Hetero)Arenes by C-H Bond Cleavage [J].
Ackermann, Lutz ;
Vicente, Ruben ;
Kapdi, Anant R. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (52) :9792-9826
[2]  
Acton A.Q., 2012, Sulfur Compounds: Advances in Research and Application
[3]   Aryl-aryl bond formation by transition-metal-catalyzed direct arylation [J].
Alberico, Dino ;
Scott, Mark E. ;
Lautens, Mark .
CHEMICAL REVIEWS, 2007, 107 (01) :174-238
[4]   Direct Use of Carboxylic Acids in the Photocatalytic Hydroacylation of Styrenes To Generate Dialkyl Ketones [J].
Alvarado, Jesus I. Martinez ;
Ertel, Alyssa B. ;
Stegner, Andrea ;
Stache, Erin E. ;
Doyle, Abigail G. .
ORGANIC LETTERS, 2019, 21 (24) :9940-9944
[5]   Carboxylic Acids as Adaptive Functional Groups in Metallaphotoredox Catalysis [J].
Beil, Sebastian B. ;
Chen, Tiffany Q. ;
Intermaggio, Nicholas E. ;
MacMillan, David W. C. .
ACCOUNTS OF CHEMICAL RESEARCH, 2022, 55 (23) :3481-3494
[6]   The modified Julia olefination:: alkene synthesis via the condensation of metallated heteroarylalkylsulfones with carbonyl compounds [J].
Blakemore, PR .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 2002, (23) :2563-2585
[7]   DECARBONYLATION OF AROMATIC CARBONYL COMPOUNDS CATALYZED BY RHODIUM COMPLEXES [J].
BLUM, J ;
OPPENHEIMER, E ;
BERGMANN, ED .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1967, 89 (10) :2338-+
[8]   Solvent cage effects. I. Effect of radical mass and size on radical cage pair recombination efficiency. II. Is geminate recombination of polar radicals sensitive to solvent polarity? [J].
Braden, DA ;
Parrack, EE ;
Tyler, DR .
COORDINATION CHEMISTRY REVIEWS, 2001, 211 :279-294
[9]   Light-driven transition-metal-free direct decarbonylation of unstrained diaryl ketones via a dual C-C bond cleavage [J].
Cao, Dawei ;
Ataya, Mohamad ;
Chen, Zhangpei ;
Zeng, Huiying ;
Peng, Yong ;
Khaliullin, Rustam Z. ;
Li, Chao-Jun .
NATURE COMMUNICATIONS, 2022, 13 (01)
[10]   Rh(I)-Catalyzed Intramolecular Decarbonylation of Thioesters [J].
Cao, Han ;
Liu, Xuejing ;
Bie, Fusheng ;
Shi, Yijun ;
Han, Ying ;
Yan, Peng ;
Szostak, Michal ;
Liu, Chengwei .
JOURNAL OF ORGANIC CHEMISTRY, 2021, 86 (15) :10829-10837