Synlett 2014; 25(19): 2717-2720
DOI: 10.1055/s-0034-1379102
cluster
© Georg Thieme Verlag Stuttgart · New York

CAN-Catalyzed Rapid C–O Bond Formation towards α-Aminoxylation of Ketones

Peng Feng
a   State Key Laboratory of Natural and Biomimetic Drugs, Peking University, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191, P. R. of China   Fax: +86(10)82805297   eMail: jiaoning@bjmu.edu.cn
,
Song Song
a   State Key Laboratory of Natural and Biomimetic Drugs, Peking University, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191, P. R. of China   Fax: +86(10)82805297   eMail: jiaoning@bjmu.edu.cn
,
Li-He Zhang
a   State Key Laboratory of Natural and Biomimetic Drugs, Peking University, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191, P. R. of China   Fax: +86(10)82805297   eMail: jiaoning@bjmu.edu.cn
,
Ning Jiao*
a   State Key Laboratory of Natural and Biomimetic Drugs, Peking University, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191, P. R. of China   Fax: +86(10)82805297   eMail: jiaoning@bjmu.edu.cn
b   Shanghai Key Laboratory of Green Chemistry and Chemical Processes, East China Normal University, Shanghai 200062, P. R. of China
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received: 03. Juli 2014

Accepted after revision: 18. August 2014

Publikationsdatum:
02. Oktober 2014 (online)


Abstract

A simple and efficient approach towards α-oxyaminated ketones has been developed through CAN-catalyzed C–O bond formation with 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO). The environmentally friendly transformation is practical due to the use of commercial available catalyst, easy operating procedures, the broad substrate scope, and short reaction time.

Supporting Information