Title:
l-Proline catalyzed condensation of salicylaldehydes with ethyl nitroacetate: an efficient access to 3-nitrocoumarins

dc.contributor.authorRajesh Kumar Sharma
dc.contributor.authorPriyanka
dc.contributor.authorDiksha Katiyar
dc.date.accessioned2026-02-07T08:15:25Z
dc.date.issued2016
dc.description.abstractAbstract: l-Proline catalyzed condensation of salicylaldehydes and ethyl nitroacetate afforded 3-nitrocoumarins in good to high yields under mild conditions. This organocatalyzed process offers a much improved yield of 3-nitrocoumarins and well tolerates both electron-donating and electron-withdrawing substituents on the phenyl ring. Graphical abstract: [Figure not available: see fulltext.] © 2016, Springer-Verlag Wien.
dc.identifier.doi10.1007/s00706-016-1736-4
dc.identifier.issn269247
dc.identifier.urihttps://doi.org/10.1007/s00706-016-1736-4
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/28602
dc.publisherSpringer-Verlag Wien
dc.subject3-Nitrocoumarins
dc.subjectCoumarins
dc.subjectl-Proline
dc.subjectOrganocatalysis
dc.subjectSalicylaldehyde
dc.titlel-Proline catalyzed condensation of salicylaldehydes with ethyl nitroacetate: an efficient access to 3-nitrocoumarins
dc.typePublication
dspace.entity.typeArticle

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