Publication:
Iodine/persulfate-promoted site-selective direct thiolation of quinolones and uracils

dc.contributor.authorDanupat Beukeawen_US
dc.contributor.authorMedena Noikhamen_US
dc.contributor.authorSirilata Yotphanen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2020-01-27T07:38:18Z
dc.date.available2020-01-27T07:38:18Z
dc.date.issued2019-09-27en_US
dc.description.abstract© 2019 Elsevier Ltd A simple and general method for direct thiolation of 4-quinolones with disulfides or thiols under I2/K2S2O8 system has been developed. Under the optimal conditions, the C–S bond coupling can take place effectively with good to decent yields and excellent regioselectivity of the S-linked products. The established metal-free site-selective approach was also applicable to transform a range of uracil substrates to the thio-substituted products under mild conditions. Further transformation to the sulfone derivatives can be conveniently performed in one-pot. These easy-to-handle protocols represent a useful and interesting synthetic alternative with good substrate scope and functional group compatibility.en_US
dc.identifier.citationTetrahedron. Vol.75, No.39 (2019)en_US
dc.identifier.doi10.1016/j.tet.2019.130537en_US
dc.identifier.issn14645416en_US
dc.identifier.issn00404020en_US
dc.identifier.other2-s2.0-85071389193en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/50071
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85071389193&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.titleIodine/persulfate-promoted site-selective direct thiolation of quinolones and uracilsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85071389193&origin=inwarden_US

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