Issue 27, 2016

Synthesis of 2-fluoro-2-pyrrolines via tandem reaction of α-trifluoromethyl-α,β-unsaturated carbonyl compounds with N-tosylated 2-aminomalonates

Abstract

A simple base-mediated tandem SN2′/SNV reaction of the readily available α-trifluoromethyl-α,β-unsaturated carbonyl compounds with N-tosylated 2-aminomalonates was developed, which provide an efficient access to functionalized tetrasubstituted 2-fluoro-2-pyrrolines in good to excellent yields. In contrast, simple 1,2-nucleophilic adducts were produced when α-trifluoromethyl styrenes were used.

Graphical abstract: Synthesis of 2-fluoro-2-pyrrolines via tandem reaction of α-trifluoromethyl-α,β-unsaturated carbonyl compounds with N-tosylated 2-aminomalonates

Supplementary files

Article information

Article type
Communication
Submitted
27 Jan 2016
Accepted
07 Mar 2016
First published
07 Mar 2016

Chem. Commun., 2016,52, 4922-4925

Synthesis of 2-fluoro-2-pyrrolines via tandem reaction of α-trifluoromethyl-α,β-unsaturated carbonyl compounds with N-tosylated 2-aminomalonates

J. Yang, X. Zhou, Y. Zeng, C. Huang, Y. Xiao and J. Zhang, Chem. Commun., 2016, 52, 4922 DOI: 10.1039/C6CC00831C

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