Title:
DMAP mediated one-pot domino thienannulation: A versatile, regioselective and green mechanochemical route to naphtho[2,3-b]thiophenes

dc.contributor.authorGaurav Shukla
dc.contributor.authorGirijesh Kumar Verma
dc.contributor.authorAnugula Nagaraju
dc.contributor.authorRajiv Kumar Verma
dc.contributor.authorKesha Raghuvanshi
dc.contributor.authorMaya Shankar Singh
dc.date.accessioned2026-02-07T05:40:21Z
dc.date.issued2013
dc.description.abstractSolvent-free mechanochemical route to naphtho[2,3-b]thiophenes via [3 + 2] oxidative heteroannulation of α-enolicdithioesters and β-oxothioamides with 1,4-naphthoquinone has been achieved at room temperature. © 2013 The Royal Society of Chemistry.
dc.identifier.doi10.1039/c3ra41100a
dc.identifier.issn20462069
dc.identifier.urihttps://doi.org/10.1039/c3ra41100a
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/24846
dc.titleDMAP mediated one-pot domino thienannulation: A versatile, regioselective and green mechanochemical route to naphtho[2,3-b]thiophenes
dc.typePublication
dspace.entity.typeArticle

Files

Collections