Taming Nitrene Reactivity with Silver Catalysts

被引:12
作者
Vine, Logan E. [1 ]
Zerull, Emily E. [1 ]
Schomaker, Jennifer M. [1 ]
机构
[1] Univ Wisconsin, Dept Chem, 1101 Univ Ave, Madison, WI 53706 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
silver; nitrene transfer; C– H functionalization; amination; amines; asymmetric; C-H AMINATION; INTERMOLECULAR AMINATION; CHEMOSELECTIVE AMINATION; COORDINATION CHEMISTRY; HETEROCYCLIC-COMPOUNDS; BOND AMINATION; GAMMA-LACTAMS; ARYL AZIDES; AZIRIDINATION; COMPLEXES;
D O I
10.1055/s-0040-1707197
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Nitrene transfer (NT) is a convenient strategy to directly transform C-H bonds into more valuable C-N bonds and exciting advances have been made to improve selectivity. Our work in silver-based NT has shown the unique ability of this metal to enable tunable chemo-, site-, and stereoselective reactions using simple N-dentate ligand scaffolds. Manipulation of the coordination environment and noncovalent interactions around the silver center furnish unprecedented catalyst control in selective NT and provide insights for further improvements in the field. 1 Introduction 1.1 Strategies for Nitrene Transfer 1.2 Brief Summary of Chemocatalyzed Nitrene Transfer 1.3 Focus of this Account 2 Challenges in Chemocatalyzed Nitrene Transfer 2.1 Reactivity Challenges 2.2 Selectivity Challenges 2.3 Chemoselective Nitrene Transfer 2.4 Site-Selective Nitrene Transfer 2.5 Enantioselective Nitrene Transfer 3 Summary and Perspective 3.1 Future Opportunities and Challenges 3.2 Conclusion
引用
收藏
页码:30 / 44
页数:15
相关论文
共 94 条
[71]   1,3-Amino alcohols and their phenol analogs in heterocyclization reactions [J].
Palchykov, Vitalii A. ;
Gaponov, Alexandr A. .
ADVANCES IN HETEROCYCLIC CHEMISTRY, VOL 131, 2020, 131 :285-350
[72]  
Paradine SM, 2015, NAT CHEM, V7, P987, DOI [10.1038/NCHEM.2366, 10.1038/nchem.2366]
[73]   Iron-Catalyzed Intramolecular Allylic C-H Amination [J].
Paradine, Shauna M. ;
White, M. Christina .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (04) :2036-2039
[74]   Asymmetric formation of γ-lactams via C-H amidation enabled by chiral hydrogen-bond-donor catalysts [J].
Park, Yoonsu ;
Chang, Sukbok .
NATURE CATALYSIS, 2019, 2 (03) :219-227
[75]  
Prier CK, 2017, NAT CHEM, V9, P629, DOI [10.1038/nchem.2783, 10.1038/NCHEM.2783]
[76]   Metal-bis(oxazoline) complexes: From coordination chemistry to asymmetric catalysis [J].
Rasappan, Ramesh ;
Laventine, Dominic ;
Reiser, Oliver .
COORDINATION CHEMISTRY REVIEWS, 2008, 252 (5-7) :702-714
[77]   Tunable, Chemoselective Amination via Silver Catalysis [J].
Rigoli, Jared W. ;
Weatherly, Cale D. ;
Alderson, Juliet M. ;
Vo, Brian T. ;
Schomaker, Jennifer M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (46) :17238-17241
[78]   1,4-Diazaspiro[2.2]pentanes as a Flexible Platform for the Synthesis of Diamine-Bearing Stereotriads [J].
Rigoli, Jared W. ;
Boralsky, Luke A. ;
Hershberger, John C. ;
Marston, Dagmara ;
Meis, Alan R. ;
Guzei, Ilia A. ;
Schomaker, Jennifer M. .
JOURNAL OF ORGANIC CHEMISTRY, 2012, 77 (05) :2446-2455
[79]   Selective Intermolecular Amination of C-H Bonds at Tertiary Carbon Centers [J].
Roizen, Jennifer L. ;
Zalatan, David N. ;
Du Bois, J. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (43) :11343-11346
[80]   Metal-Catalyzed Nitrogen-Atom Transfer Methods for the Oxidation of Aliphatic C-H Bonds [J].
Roizen, Jennifer L. ;
Harvey, Mark Edwin ;
Du Bois, J. .
ACCOUNTS OF CHEMICAL RESEARCH, 2012, 45 (06) :911-922