Radical-Mediated Approaches for the Synthesis of Thiolactones

被引:4
作者
McCourt, Ruairi O. [1 ]
Scanlan, Eoin M. [1 ]
机构
[1] Univ Dublin, Dept Sch Chem, Trinity Biomed Sci Inst TBSI, Dublin 2, Ireland
基金
爱尔兰科学基金会;
关键词
Cyclizations; Hetercycles; Radicals; Thioacids; Thiolactone; HOMOCYSTEINE THIOLACTONE; THIOL-ENE; STAPHYLOCOCCUS-AUREUS; BETA-THIOLACTONES; CHEMISTRY; MECHANISM; CYCLIZATION; SULFUR; ACID; PHOTOCHEMISTRY;
D O I
10.1002/ejoc.202100996
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In this review we discuss the diverse synthetic approaches and methodologies which have been utilized for the preparation of small and medium ring thiolactones via radical-mediated processes. We provide a brief overview of the major current applications and uses of thiolactones in disparate fields of study and outline a selection of representative methods which have been employed for the preparation of compounds containing this structural motif, with a concise consideration of the conditions employed, the key intermediates formed and the mechanism of the transformations, where pertinent. Reaction classification has been broadly divided into two distinct classes: those in which the key bond forming step is an intermolecular radical process, and those in which it is an intramolecular process (radical cyclization). Both of these reaction classes may be further subdivided into processes that proceed via a carbon-centered (C-centered) radical, and those that proceed through a thiyl/sulfur-centered (S-centered) radical.
引用
收藏
页码:5320 / 5334
页数:15
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