Issue 30, 2017

Comment on “An unexpected formation of the novel 7-oxa-2-azabicyclo[2.2.1]hept-5-ene skeleton during the reaction of furfurylamine with maleimides and their bioprospection using a zebrafish embryo model” by C. E. Puerto Galvis and V. V. Kouznetsov, Org. Biomol. Chem., 2013, 11, 407

Abstract

It has been proved that the reaction between furfuryl amines and N-R-maleimides leads to the formation of aza-Michael addition products – 3-(furylmethylamino)-N-R-pyrrolidine-2,5-diones, instead of 7-oxa-2-azabicyclo[2.2.1]hept-5-enes, as this journal reported previously.

Graphical abstract: Comment on “An unexpected formation of the novel 7-oxa-2-azabicyclo[2.2.1]hept-5-ene skeleton during the reaction of furfurylamine with maleimides and their bioprospection using a zebrafish embryo model” by C. E. Puerto Galvis and V. V. Kouznetsov, Org. Biomol. Chem., 2013, 11, 407

Associated articles

Supplementary files

Article information

Article type
Comment
Submitted
17 May 2017
Accepted
10 Jul 2017
First published
10 Jul 2017
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2017,15, 6447-6450

Comment on “An unexpected formation of the novel 7-oxa-2-azabicyclo[2.2.1]hept-5-ene skeleton during the reaction of furfurylamine with maleimides and their bioprospection using a zebrafish embryo model” by C. E. Puerto Galvis and V. V. Kouznetsov, Org. Biomol. Chem., 2013, 11, 407

F. I. Zubkov, E. A. Kvyatkovskaya, E. V. Nikitina, P. N.-A. Amoyaw, V. V. Kouznetsov, V. A. Lazarenko and V. N. Khrustalev, Org. Biomol. Chem., 2017, 15, 6447 DOI: 10.1039/C7OB01207A

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