A Need for Caution in the Preparation and Application of Synthetically Versatile Aryl Diazonium Tetrafluoroborate Salts

被引:100
作者
Firth, James D.
Fairlamb, Ian J. S.
机构
[1] Department of Chemistry, University of York, York, Heslington
基金
英国工程与自然科学研究理事会;
关键词
METAL-FREE; ARYLATION; ROUTE; GREEN;
D O I
10.1021/acs.orglett.0c02685
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:7057 / 7059
页数:3
相关论文
共 34 条
[1]  
[Anonymous], 1967, CHEM ENG NEWS, V45, P44
[2]   Merck's Reaction Review Policy: An Exercise in Process Safety [J].
Bassan, Ephraim ;
Ruck, Rebecca T. ;
Dienemann, Erik ;
Emerson, Khateeta M. ;
Humphrey, Guy R. ;
Raheem, Izzat T. ;
Tschaen, David M. ;
Vickery, Thomas P. ;
Wood, Harold B. ;
Yasuda, Nobuyoshi .
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2013, 17 (12) :1611-1616
[3]   Pd(NHC)PEPPSI-diazonium salts: an efficient blend for the decarboxylative Sonogashira cross coupling reaction [J].
Bhojane, Jeevan Manohar ;
Jadhav, Vitas Gangadhar ;
Nagarkar, Jayashree Milind .
NEW JOURNAL OF CHEMISTRY, 2017, 41 (14) :6775-6780
[4]   Aryl Diazonium versus Iodonium Salts: Preparation, Applications and Mechanisms for the Suzuki-Miyaura Cross-Coupling Reaction [J].
Bonin, Helene ;
Fouquet, Eric ;
Felpin, Francois-Xavier .
ADVANCED SYNTHESIS & CATALYSIS, 2011, 353 (17) :3063-3084
[5]   Aryldiazonium Tetrafluoroborate Salts as Green and Efficient Coupling Partners for the Suzuki-Miyaura Reaction: From Optimisation to Mole Scale [J].
Colleville, Aymeric P. ;
Horan, Richard A. J. ;
Tornkinson, Nicholas C. O. .
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2014, 18 (09) :1128-1136
[6]  
DOAK GO, 1967, CHEM ENG NEWS, V45, P8
[7]   How the Structural Elucidation of the Natural Product Stephanosporin Led to New Developments in Aryl Radical and Medicinal Chemistry [J].
Fehler, Stefanie K. ;
Heinrich, Markus R. .
SYNLETT, 2015, 26 (05) :580-603
[8]   Biaryl synthesis with arenediazonium salts: cross-coupling, CH-arylation and annulation reactions [J].
Felpin, Francois-Xavier ;
Sengupta, Saumitra .
CHEMICAL SOCIETY REVIEWS, 2019, 48 (04) :1150-1193
[9]  
Griefs P., 1858, ANN CHEM PHARM, V106, P123, DOI DOI 10.1002/(ISSN)1099-0690
[10]   THE SANDMEYER REACTION [J].
HODGSON, HH .
CHEMICAL REVIEWS, 1947, 40 (02) :251-277