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dc.contributor.authorSirawit Wet-Osoten_US
dc.contributor.authorMookda Pattarawarapanen_US
dc.contributor.authorWong Phakhodeeen_US
dc.date.accessioned2018-09-04T10:07:41Z-
dc.date.available2018-09-04T10:07:41Z-
dc.date.issued2015-12-30en_US
dc.identifier.issn18733581en_US
dc.identifier.issn00404039en_US
dc.identifier.other2-s2.0-84949106013en_US
dc.identifier.other10.1016/j.tetlet.2015.11.038en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84949106013&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/54095-
dc.description.abstract© 2015 Elsevier Ltd. All rights reserved. A convenient one-pot, two-step procedure for the synthesis of ketone cyanohydrin esters in aqueous media is reported using N-acylbenzotriazoles as the acylating agents. In saturated aqueous sodium bicarbonate containing a catalytic amount of tetrabutylammonium bromide, the reaction of ketones with potassium cyanide and N-acylbenzotriazoles proceeded readily at room temperature to provide the corresponding O-acyl cyanohydrin derivatives in good to excellent yields.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA convenient one-pot synthesis of ketone cyanohydrin esters in aqueous mediaen_US
dc.typeJournalen_US
article.title.sourcetitleTetrahedron Lettersen_US
article.volume56en_US
article.stream.affiliationsChiang Mai Universityen_US
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