Issue 45, 2016

Silver-catalyzed nucleophilic substitution of aminals with ethyl diazoacetate: a new pathway to β-amino-α-diazoesters

Abstract

A novel silver-catalyzed nucleophilic substitution of aminals with ethyl diazoacetate producing β-amino-α-diazoesters has been developed. A series of aminals with different amino moieties and substituents were successfully incorporated in this reaction, which delivered a wide range of β-amino-α-diazocarbonyl compounds in the presence of a lower catalyst loading in 2 hours.

Graphical abstract: Silver-catalyzed nucleophilic substitution of aminals with ethyl diazoacetate: a new pathway to β-amino-α-diazoesters

Supplementary files

Article information

Article type
Communication
Submitted
01 Oct 2016
Accepted
20 Oct 2016
First published
20 Oct 2016

Org. Biomol. Chem., 2016,14, 10572-10575

Silver-catalyzed nucleophilic substitution of aminals with ethyl diazoacetate: a new pathway to β-amino-α-diazoesters

J. Li, G. Qin and H. Huang, Org. Biomol. Chem., 2016, 14, 10572 DOI: 10.1039/C6OB02136K

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