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- W3200208081 endingPage "1081" @default.
- W3200208081 startingPage "1081" @default.
- W3200208081 abstract "Isothiocyanates (ITCs) are biologically active molecules found in several natural products and pharmaceutical ingredients. Moreover, due to their high and versatile reactivity, they are widely used as intermediates in organic synthesis. This review considers the best practices for the synthesis of ITCs using elemental sulfur, highlighting recent developments. First, we summarize the in situ generation of thiocarbonyl surrogates followed by their transformation in the presence of primary amines leading to ITCs. Second, carbenes and amines afford isocyanides, and the further reaction of this species with sulfur readily generates ITCs under thermal, catalytic or basic conditions. Additionally, we also reveal that in the catalyst-free reaction of isocyanides and sulfur, two—until this time overlooked and not investigated—different mechanistic pathways exist." @default.
- W3200208081 created "2021-09-27" @default.
- W3200208081 creator A5011278193 @default.
- W3200208081 creator A5077916560 @default.
- W3200208081 date "2021-09-08" @default.
- W3200208081 modified "2023-10-07" @default.
- W3200208081 title "Recent Advances in the Synthesis of Isothiocyanates Using Elemental Sulfur" @default.
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- W3200208081 doi "https://doi.org/10.3390/catal11091081" @default.
- W3200208081 hasPublicationYear "2021" @default.
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