Synthesis of -β-brominated alkenyl isothiocyanates dehydrogenation of alkyl isothiocyanates

This study presents a new dehydrogenative synthesis of alkenyl isothiocyanates, providing compounds with bromo and isothiocyanate groups. These reactive functionalities offer versatility for further transformations. Application in an amine sensor utilizing a coumarin-attached product demonstrates pr...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2024-06, Vol.6 (47), p.615-618
Hauptverfasser: Maeda, Bumpei, Akiyoshi, Ryohei, Tanaka, Daisuke, Sato, Kohei, Murakami, Kei
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Zusammenfassung:This study presents a new dehydrogenative synthesis of alkenyl isothiocyanates, providing compounds with bromo and isothiocyanate groups. These reactive functionalities offer versatility for further transformations. Application in an amine sensor utilizing a coumarin-attached product demonstrates practical utility. This streamlined approach facilitates access to alkenyl isothiocyanates, valuable tools for biological studies. A new dehydrogenative synthesis of alkenyl isothiocyanates has been developed; the reaction provides compounds with bromo and isothiocyanate groups. The products are applicable to various further transformations.
ISSN:1359-7345
1364-548X
DOI:10.1039/d4cc01666a