Synthesis of the 1,5-Benzothiazepane Scaffold - Established Methods and New Developments

被引:2
作者
Ronse, Ulrike [1 ]
Magdalenic, Katarina [1 ]
Van Camp, John [2 ]
D'hooghe, Matthias [1 ]
机构
[1] Univ Ghent, Fac Biosci Engn, Dept Green Chem & Technol, SynBioC Res Grp, Coupure Links 653, B-9000 Ghent, Belgium
[2] Univ Ghent, Dept Food Technol Safety & Hlth, Coupure Links 653, B-9000 Ghent, Belgium
关键词
benzothiazepanes; biological activity; heterocycles; sustainable chemistry; synthetic methods; CATALYST-FREE SYNTHESIS; RING-EXPANSION; ENANTIOSELECTIVE SYNTHESIS; REGIOSELECTIVE SYNTHESIS; BIOLOGICAL EVALUATION; DERIVATIVES; NITROGEN; ACCESS; HETEROCYCLES; CONDENSATION;
D O I
10.1002/open.202200262
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The 1,5-benzothiazepane structure is an important heterocyclic moiety present in a variety of commercial drugs and pharmaceuticals. This privileged scaffold exhibits a diversity of biological activities, including antimicrobial, antibacterial, anti-epileptic, anti-HIV, antidepressant, antithrombotic and anticancer properties. Its important pharmacological potential renders research into the development of new and efficient synthetic methods of high relevance. In the first part of this review, an overview of different synthetic approaches toward 1,5-benzothiazepane and its derivatives is provided, ranging from established protocols to recent (enantioselective) methods that promote sustainability. In the second part, several structural characteristics influencing biological activity are briefly explored, providing a few insights into the structure-activity relationships of these compounds.
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页数:18
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