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박철민

Park, Cheol-Min
Synthetic and Medicinal Chemistry Lab.
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Synthesis of dithioacetals via gold-catalysed hydrothiolation of vinyl sulfides

Author(s)
Murugesh, VenkateshRyou, BokyeongPark, Cheol-Min
Issued Date
2023-01
DOI
10.1039/d2ob01737g
URI
https://scholarworks.unist.ac.kr/handle/201301/61594
Citation
ORGANIC & BIOMOLECULAR CHEMISTRY, v.21, no.3, pp.585 - 589
Abstract
The synthesis of unsymmetrical dithioacetals based on gold catalysis is described. Although many approaches to the preparation of symmetrical dithioacetals have been developed, the methods to access unsymmetrical ones remain limited. In this regard, we report a mild synthetic method with a broad substrate scope. Screening of various gold catalysts identified a catalyst, which allows the hydrothiolation of both activated and unactivated vinyl sulfides with high efficiency. Moreover, the reaction displays broad compatibility for both aryl and aliphatic thiols.
Publisher
ROYAL SOC CHEMISTRY
ISSN
1477-0520
Keyword
SULFENYLATED CARBONYL-COMPOUNDSPROPARGYLIC ALCOHOLSBOND FORMATIONC-SMETALTHIOLSALKYNESALKENES1,3-DITHIANESDERIVATIVES

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