Recent advances in fluoride-free aryne generation from arene precursors

被引:73
|
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
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