{"title":"生物活性有机二硫代氨基甲酸酯合成方法的最新进展","authors":"Babli Roy","doi":"10.1080/17415993.2025.2497317","DOIUrl":null,"url":null,"abstract":"<div><div>The chemically and medicinally versatile dithiocarbamates play a significant role in advancing various fields, including agriculture, chemical synthesis, and environmental remediation. However, dithiocarbamates have primarily been utilised as pesticides and fungicides for crop protection since the 1930s. Recently, the revival of dithiocarbamates from agrochemicals to repurposed drugs for treating life-threatening diseases like cancer and microbial infections has stimulated medicinal chemists to reinvestigate their unmet potential. Furthermore, dithiocarbamates containing diversified organic functionalities have shown promising antifungal activity against fungal-resistant phytopathogens, offering a solution to addressing the global threat of fungal resistance. Consequently, the synthesis of multifaceted S and N-functionalized organic dithiocarbamates using diverse organic substrates has resurfaced in synthetic and medicinal chemistry research. There is also a growing trend to develop more convenient synthetic approaches for synthesising organic dithiocarbamates featuring various green chemistry aspects, including alternative or renewable energy resources, green solvents, solvent-free reaction conditions, and cost-effectiveness. These greener approaches are also associated with high efficiency, better selectivity, broad substrate scope, outstanding yields, operational simplicity, and viability. This review provides an in-depth overview of the recent developments in the diverse synthetic routes for preparing novel organic dithiocarbamates, including multi-component approaches involving the reaction of amines, carbon disulfide, and a wide range of organic substrates. The emerging methodologies for directly synthesising S-alkyl and S-aryl dithiocarbamates using commercially available and non-hazardous tetraalkylthiuram disulfides or monosulfides as organic precursors are also comprehensively discussed in this article. This review also highlights recently developed unconventional greener protocols using alternative reactants instead of carbon disulfide or thiuram disulfides.</div></div>","PeriodicalId":17081,"journal":{"name":"Journal of Sulfur Chemistry","volume":"46 5","pages":"Pages 922-974"},"PeriodicalIF":1.6000,"publicationDate":"2025-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Recent advances in synthetic approaches for biologically active organic dithiocarbamates\",\"authors\":\"Babli Roy\",\"doi\":\"10.1080/17415993.2025.2497317\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The chemically and medicinally versatile dithiocarbamates play a significant role in advancing various fields, including agriculture, chemical synthesis, and environmental remediation. However, dithiocarbamates have primarily been utilised as pesticides and fungicides for crop protection since the 1930s. Recently, the revival of dithiocarbamates from agrochemicals to repurposed drugs for treating life-threatening diseases like cancer and microbial infections has stimulated medicinal chemists to reinvestigate their unmet potential. Furthermore, dithiocarbamates containing diversified organic functionalities have shown promising antifungal activity against fungal-resistant phytopathogens, offering a solution to addressing the global threat of fungal resistance. Consequently, the synthesis of multifaceted S and N-functionalized organic dithiocarbamates using diverse organic substrates has resurfaced in synthetic and medicinal chemistry research. There is also a growing trend to develop more convenient synthetic approaches for synthesising organic dithiocarbamates featuring various green chemistry aspects, including alternative or renewable energy resources, green solvents, solvent-free reaction conditions, and cost-effectiveness. These greener approaches are also associated with high efficiency, better selectivity, broad substrate scope, outstanding yields, operational simplicity, and viability. This review provides an in-depth overview of the recent developments in the diverse synthetic routes for preparing novel organic dithiocarbamates, including multi-component approaches involving the reaction of amines, carbon disulfide, and a wide range of organic substrates. The emerging methodologies for directly synthesising S-alkyl and S-aryl dithiocarbamates using commercially available and non-hazardous tetraalkylthiuram disulfides or monosulfides as organic precursors are also comprehensively discussed in this article. This review also highlights recently developed unconventional greener protocols using alternative reactants instead of carbon disulfide or thiuram disulfides.</div></div>\",\"PeriodicalId\":17081,\"journal\":{\"name\":\"Journal of Sulfur Chemistry\",\"volume\":\"46 5\",\"pages\":\"Pages 922-974\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-09-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Sulfur Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1741599325000261\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Sulfur Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1741599325000261","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Recent advances in synthetic approaches for biologically active organic dithiocarbamates
The chemically and medicinally versatile dithiocarbamates play a significant role in advancing various fields, including agriculture, chemical synthesis, and environmental remediation. However, dithiocarbamates have primarily been utilised as pesticides and fungicides for crop protection since the 1930s. Recently, the revival of dithiocarbamates from agrochemicals to repurposed drugs for treating life-threatening diseases like cancer and microbial infections has stimulated medicinal chemists to reinvestigate their unmet potential. Furthermore, dithiocarbamates containing diversified organic functionalities have shown promising antifungal activity against fungal-resistant phytopathogens, offering a solution to addressing the global threat of fungal resistance. Consequently, the synthesis of multifaceted S and N-functionalized organic dithiocarbamates using diverse organic substrates has resurfaced in synthetic and medicinal chemistry research. There is also a growing trend to develop more convenient synthetic approaches for synthesising organic dithiocarbamates featuring various green chemistry aspects, including alternative or renewable energy resources, green solvents, solvent-free reaction conditions, and cost-effectiveness. These greener approaches are also associated with high efficiency, better selectivity, broad substrate scope, outstanding yields, operational simplicity, and viability. This review provides an in-depth overview of the recent developments in the diverse synthetic routes for preparing novel organic dithiocarbamates, including multi-component approaches involving the reaction of amines, carbon disulfide, and a wide range of organic substrates. The emerging methodologies for directly synthesising S-alkyl and S-aryl dithiocarbamates using commercially available and non-hazardous tetraalkylthiuram disulfides or monosulfides as organic precursors are also comprehensively discussed in this article. This review also highlights recently developed unconventional greener protocols using alternative reactants instead of carbon disulfide or thiuram disulfides.
期刊介绍:
The Journal of Sulfur Chemistry is an international journal for the dissemination of scientific results in the rapidly expanding realm of sulfur chemistry. The journal publishes high quality reviews, full papers and communications in the following areas: organic and inorganic chemistry, industrial chemistry, materials and polymer chemistry, biological chemistry and interdisciplinary studies directly related to sulfur science.
Papers outlining theoretical, physical, mechanistic or synthetic studies pertaining to sulfur chemistry are welcome. Hence the target audience is made up of academic and industrial chemists with peripheral or focused interests in sulfur chemistry. Manuscripts that truly define the aims of the journal include, but are not limited to, those that offer: a) innovative use of sulfur reagents; b) new synthetic approaches to sulfur-containing biomolecules, materials or organic and organometallic compounds; c) theoretical and physical studies that facilitate the understanding of sulfur structure, bonding or reactivity; d) catalytic, selective, synthetically useful or noteworthy transformations of sulfur containing molecules; e) industrial applications of sulfur chemistry; f) unique sulfur atom or molecule involvement in interfacial phenomena; g) descriptions of solid phase or combinatorial methods involving sulfur containing substrates. Submissions pertaining to related atoms such as selenium and tellurium are also welcome. Articles offering routine heterocycle formation through established reactions of sulfur containing substrates are outside the scope of the journal.