Synlett 2016; 27(10): 1592-1596
DOI: 10.1055/s-0035-1561582
letter
© Georg Thieme Verlag Stuttgart · New York

Iodine-Mediated Oxidative Dehydrogenation of β-Acylamino Ketones for the Highly Stereoselective Synthesis of (Z)-β-Keto­enamides

Hong-Hong Chang
a   College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, P. R. of China   Email: gaowenchao@tyut.edu.cn
,
Fei Hu
a   College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, P. R. of China   Email: gaowenchao@tyut.edu.cn
,
Wen-Chao Gao*
a   College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, P. R. of China   Email: gaowenchao@tyut.edu.cn
,
Tao Liu
a   College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, P. R. of China   Email: gaowenchao@tyut.edu.cn
,
Xing Li
a   College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, P. R. of China   Email: gaowenchao@tyut.edu.cn
,
Wen-Long Wei
a   College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024, P. R. of China   Email: gaowenchao@tyut.edu.cn
,
Yan Qiao*
b   State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, P. R. of China   Email: qiaoy@sxicc.ac.cn
› Author Affiliations
Further Information

Publication History

Received: 14 January 2016

Accepted after revision: 26 February 2016

Publication Date:
14 March 2016 (online)


Preview

Abstract

An iodine-mediated oxidative dehydrogenation of β-acylamino ketones has been developed for the synthesis of β-ketoenamides in moderate to good yields. Only Z-isomers are accessed due to the intramolecular H-bonding interaction in the HI-elimination step.

Supporting Information