Recent advances in reactions between arynes and organosulfur compounds

被引:70
|
作者
Matsuzawa, Tsubasa [1 ]
Yoshida, Suguru [1 ]
Hosoya, Takamitsu [1 ]
机构
[1] TMDU, Inst Biomat & Bioengn, Lab Chem Biosci, Chiyoda Ku, 2-3-10 Kanda Surugadai, Tokyo 1010062, Japan
关键词
Aryne intermediates; Organosulfurs; Addition reactions; Rearrangement; Diversity-oriented synthesis; C-H ACTIVATION; BOND FORMATION; FACILE ACCESS; TRIARYLSULFONIUM SALTS; STEVENS REARRANGEMENT; EFFICIENT GENERATION; DIRECT THIOAMINATION; MODULAR SYNTHESIS; ARYL TRIFLONES; INSERTION;
D O I
10.1016/j.tetlet.2018.10.031
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The recent progress made on transformations involving the reactions between aryne intermediates and organosulfur compounds has been reviewed. A wide variety of aromatic organosulfurs are now synthesizable by generating arynes in the presence of organosulfur compounds. Organosulfurs have distinctive reactivities with arynes, which depend on the sulfur atom's valence state, that is, S(II), S(IV), and S(VI), as well as the presence or absence of other intra- or intermolecular reactive moieties. These novel transformations have enabled the diversity-oriented synthesis of unique aromatic organosulfurs that were once difficult to prepare by the conventional methods, paving the way for the development of molecules that are beneficial across numerous disciplines, including pharmaceutical science and materials science. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4197 / 4208
页数:12
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