Recent advances in fluoride-free aryne generation from arene precursors

被引:82
作者
Idiris, Fahima I. M. [1 ]
Jones, Christopher R. [1 ]
机构
[1] Queen Mary Univ London, Sch Biol & Chem Sci, Mile End Rd, London E1 4NS, England
基金
英国工程与自然科学研究理事会;
关键词
DIELS-ALDER REACTION; ONE-POT SYNTHESIS; GRIGNARD-REAGENTS; ORGANIC-SYNTHESIS; ROOM-TEMPERATURE; NATURAL-PRODUCTS; BENZYNE; CHEMISTRY; TRIPHENYLENES; BORYLATION;
D O I
10.1039/c7ob01947e
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Aryne chemistry has experienced a remarkable renaissance in recent years, with a significant increase in the synthetic applications reported for these highly valuable reactive intermediates. This resurgence of interest is in part due to the introduction of ortho-silylaryl triflates as precursors which can be activated under mild conditions using fluoride. Alternative fluoride-free strategies have received interest in the last decade, with a number of precursors to arynes and their activators reported. These approaches offer alternative modes of reactivity which prove, in some cases, to be orthogonal to those of ortho-silylaryl triflates. This review highlights some of the more recent fluoride-free methodologies developed to access aryne intermediates that start from arene-based precursors.
引用
收藏
页码:9044 / 9056
页数:13
相关论文
共 79 条
[1]   ARYLATION OF TETRAZOLIDE WITH DIARYLIODONIUM HALIDES - EVIDENCE FOR INTERMEDIACY OF BENZYNE [J].
AKIYAMA, T ;
IMASAKI, Y ;
KAWANISI, M .
CHEMISTRY LETTERS, 1974, (03) :229-230
[2]  
[Anonymous], SCI SPECTRA
[3]  
Antonio J., 2014, ORG LETT, V16, P2338
[4]   Employing Arynes in Diels-Alder Reactions and Transition-Metal-Free Multicomponent Coupling and Arylation Reactions [J].
Bhojgude, Sachin Suresh ;
Bhunia, Anup ;
Biju, Akkattu T. .
ACCOUNTS OF CHEMICAL RESEARCH, 2016, 49 (09) :1658-1670
[5]   Recent advances in transition-metal-free carbon-carbon and carbon-heteroatom bond-forming reactions using arynes [J].
Bhunia, Anup ;
Yetra, Santhivardhana Reddy ;
Biju, Akkattu T. .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (08) :3140-3152
[6]   High-yielding one-pot synthesis of diaryliodonium triflates from arenes and iodine or aryl iodides [J].
Bielawski, Marcin ;
Olofsson, Berit .
CHEMICAL COMMUNICATIONS, 2007, (24) :2521-2523
[7]   Silyl-directed, iridium-catalyzed ortho-borylation of arenes. A one-pot ortho-borylation of phenols, arylamines, and alkylarenes [J].
Boebel, Timothy A. ;
Hartwig, John. F. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (24) :7534-+
[8]   Thermolysis of 1,3,8-nonatriyne: Evidence for intramolecular [2+4] cycloaromatization to a benzyne intermediate [J].
Bradley, AZ ;
Johnson, RP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (41) :9917-9918
[9]   THE PREPARATION, REACTIONS, AND PROPERTIES OF TRIPHENYLENES [J].
BUESS, CM ;
LAWSON, DD .
CHEMICAL REVIEWS, 1960, 60 (04) :313-330
[10]   REACTIVE INTERMEDIATES .I. SYNTHESIS AND OXIDATION OF 1- AND 2-AMINOBENZOTRIAZOLE [J].
CAMPBELL, CD ;
REES, CW .
JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC, 1969, (05) :742-&