6052-18-2Relevant articles and documents
The intramolecular Diels-Alder vinylfuran (IMDAV) reaction: a short approach to aza-analogues of pinguisane-type sesquiterpenes
Horak, Yuriy I.,Lytvyn, Roman Z.,Homza, Yuriy V.,Zaytsev, Vladimir P.,Mertsalov, Dmitriy F.,Babkina, Maria N.,Nikitina, Eugenia V.,Lis, Tadeusz,Kinzhybalo, Vasyl,Matiychuk, Vasyl S.,Zubkov, Fedor I.,Varlamov, Alexey V.,Obushak, Mykola D.
, p. 4499 - 4501 (2015)
Abstract The reaction of readily accessible (3-furyl)allylamines with maleic anhydride, followed by a domino sequence involving acylation/cycloaddition/proton shift steps, led to the formation of furo[2,3-f]isoindoles - the aza-analogs of pinguisane-type
Easy construction of furo[2,3-f]isoindole core by the IMDAV reaction between 3-(furyl)allylamines and α,β-unsaturated acid anhydrides
Zubkov, Fedor I.,Zaytsev, Vladimir P.,Mertsalov, Dmitriy F.,Nikitina, Eugenia V.,Horak, Yuriy I.,Lytvyn, Roman Z.,Homza, Yuriy V.,Obushak, Mykola D.,Dorovatovskii, Pavel V.,Khrustalev, Victor N.,Varlamov, Alexey V.
, p. 2239 - 2253 (2016/04/19)
The vinylogues of furfurylamines, easily available in two steps from furylacroleins (3-(furyl)allylamines), were studied in a tandem N-acylation/intramolecular [4+2] cycloaddition with maleic, pyrocinchonic, and citraconic anhydrides, as well as furylacry
Synthesis of Schiff's bases from furylacroleins and aminopyridines in the presence of molecular sieves
Iovel,Golomba,Popelis,Gaukhman,Lukevics
, p. 264 - 274 (2007/10/03)
We have studied the reactions of (hetero)aromatic aldehydes with 2-aminopyridines. The results obtained suggest that molecular sieves play a role in these processes not only as a dehydrating agent but also as an acid catalyst. We have synthesized a series of novel heterocyclic azomethines.
