Recent advancement in the synthesis of isothiocyanates

被引:5
|
作者
Maeda, Bumpei [1 ]
Murakami, Kei [1 ,2 ]
机构
[1] Kwansei Gakuin Univ, Sch Sci, Dept Chem, Sanda, Hyogo 6691330, Japan
[2] Japanese Sci & Technol Agcy JST PRESTO, Tokyo 1020076, Japan
基金
日本科学技术振兴机构;
关键词
H BOND FUNCTIONALIZATION; EFFICIENT SYNTHESIS; MEDIATED DESULFURIZATION; DIETARY ISOTHIOCYANATES; UNSYMMETRICAL THIOUREAS; ARYL ISOTHIOCYANATES; PRIMARY AMINES; REAGENT; CHEMISTRY; CANCER;
D O I
10.1039/d3cc06118c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Isothiocyanates exhibit various biological characteristics, including antimicrobial, anti-inflammatory, and anticancer properties. Their significance extends to synthetic chemistry, where they serve as valuable platforms for versatile transformations. Consequently, they have attracted the attention of biologists and chemists. This review summarizes recent advancements in the synthesis of isothiocyanates. Access to a variety of starting materials is important to prepare isothiocyanates with diverse structures. This review categorizes synthetic methods into three types based on the starting materials and functional groups: (i) type A, derived from primary amines; (ii) type B, derived from other nitrogen functional groups; and (iii) type C, derived from non-nitrogen groups. Recent trends in synthetic methods have revealed the prevalence of type-A reactions derived from primary amines. However, type B reactions have rarely been reported. Notably, over the past four years, there has been a notable increase in type C reactions, indicating a growing interest in non-nitrogen-derived isothiocyanates. Overall, this review not only outlines the advancements in the synthesis of isothiocyanates but also highlights trends in the methodology. Isothiocyanates exhibit diverse bioactivities and reactivities. This review describes a comprehensive summary of recent advances in isothiocyanate synthesis with a focus on substrate categorization.
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页码:2839 / 2864
页数:26
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