Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/54095
Title: A convenient one-pot synthesis of ketone cyanohydrin esters in aqueous media
Authors: Sirawit Wet-Osot
Mookda Pattarawarapan
Wong Phakhodee
Keywords: Biochemistry, Genetics and Molecular Biology
Chemistry
Pharmacology, Toxicology and Pharmaceutics
Issue Date: 30-Dec-2015
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.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84949106013&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/54095
ISSN: 18733581
00404039
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.