Stereoselective sulfenylation of oxindole-derived propargyl alcohols to access sulfenylated-3-alkenyloxindoles

dc.contributor.author Khan, Tabassum
dc.contributor.author Rajesh, Pallava
dc.contributor.author Arun, Doma
dc.contributor.author Yaragorla, Srinivasarao
dc.date.accessioned 2022-03-27T08:48:59Z
dc.date.available 2022-03-27T08:48:59Z
dc.date.issued 2021-12-14
dc.description.abstract A Ca-catalyzed, tetrasubstituted alkenyl-sulfenylation was achieved using readily available aryl/alkyl thiols and easily prepared oxindole-derived propargyl alcohols under solvent-free conditions. The reaction proceeded with hydrogen bonding assisted regioselective α-thiolation and subsequent calcium catalyzed stereoselective alkenylation to yield E-alkenyl thioethers with high diastereoselectivity. This journal is
dc.identifier.citation Organic and Biomolecular Chemistry. v.19(46)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/d1ob01921j
dc.identifier.uri http://xlink.rsc.org/?DOI=D1OB01921J
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11855
dc.title Stereoselective sulfenylation of oxindole-derived propargyl alcohols to access sulfenylated-3-alkenyloxindoles
dc.type Journal. Article
dspace.entity.type
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