78073-03-7Relevant academic research and scientific papers
Furan ring opening-pyrrole ring closure. A simple route to 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-3-ones
Trushkov, Igor V.,Nevolina, Tatyana A.,Shcherbinin, Vitaly A.,Sorotskaya, Lyudmila N.,Butin, Alexander V.
, p. 3974 - 3976 (2013/07/25)
We report here an application of a furan ring opening-Paal-Knorr pyrrole synthesis sequence for the transformation of furfurylamines into 1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazin-3-ones.
Europium(III) triflate-catalyzed Trofimov synthesis of polyfunctionalized pyrroles
Madabhushi, Sridhar,Vangipuram, Venkata Sairam,Mallu, Kishore Kumar Reddy,Chinthala, Narsaiah,Beeram, China Ramanaiah
supporting information; body text, p. 1413 - 1416 (2012/07/13)
The synthesis of polyfunctionalized pyrroles by reaction of a ketoxime with dimethyl acetylenedicarboxylate using europium(III) triflate as the catalyst is described. Copyright
FURAN AND PYRROLE CONTAINING LIPOXYGENASE INHIBITING COMPOUNDS
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, (2008/06/13)
Substituted furan and pyrrole compounds which are useful in inhibiting lipoxygenase enzymes, particularly 5-lipoxygenase.
Substituted furan compounds which are useful in inhibiting lipoxygenase enzymes, particularly 5-lipoxygenase
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, (2008/06/13)
Substituted furan and pyrrole compounds of formula (I) which are useful in inhibiting lipoxygenase enzymes, particuarly 5-lipoxygenase.
gem-DIALKOXYLATION OF 2-ACETYLTHIOPHENES AND 2-ACETYLFURANS
Gordeeva, G. N.,Kalashnikov, S. M.,Popov, Yu. N.,Kruglov, E. A.,Imashev, U. B.
, p. 638 - 641 (2007/10/02)
Reaction of 2-acetyl-substituted thiophenes and furans with alkyl nitrites in the presence of the corresponding aliphatic alcohols and hydrochloric acid leads to the formation of linear acetals of thienyl- and furylglyoxals, whose structure was established by IR, UV, NMR spectroscopy, and mass spectrometry methods.The main paths of the dissociation of the molecules under electron impact were established.
