Highly regioselective organocatalyzed synthesis of pyrazoles from diazoacetates and carbonyl compounds
…, J Huang, X Gong, J Wang
Index: Wang, Lei; Huang, Jiayao; Gong, Xiaojie; Wang, Jian Chemistry - A European Journal, 2013 , vol. 19, # 23 p. 7555 - 7560
Full Text: HTML
Citation Number: 1
Abstract
Abstract A general, organocatalytic inverse-electron-demand [3+ 2] cycloaddition reaction between a range of carbonyl compounds and diazoacetates has been developed. This reaction is catalyzed by secondary amines as a “green promoter” to generate substituted pyrazoles with high levels of regioselectivity. It is noteworthy that this [3+ 2] cycloaddition reaction proceeds efficiently at room temperature with a simple and inexpensive catalyst. ...
Related Articles:
[Doyle, Michael P.; Colsman, Mark R.; Dorow, Roberta L. Journal of Heterocyclic Chemistry, 1983 , vol. 20, p. 943 - 946]
[Padwa, Albert; Kulkarni, Yashwant S.; Zhang, Zhijia Journal of Organic Chemistry, 1990 , vol. 55, # 13 p. 4144 - 4153]
[Padwa, Albert; Kulkarni, Yashwant S.; Zhang, Zhijia Journal of Organic Chemistry, 1990 , vol. 55, # 13 p. 4144 - 4153]