Stereoselective synthesis of sugar fused β-disubstituted γ-butyro-lactones: C-spiro-glycosides from 1,2-cyclopropanecarboxylated sugars

dc.contributor.author Ramu Sridhar, Perali
dc.contributor.author Seshadri, Kalapati
dc.contributor.author Madhusudhan Reddy, Gadi
dc.date.accessioned 2022-03-27T08:37:36Z
dc.date.available 2022-03-27T08:37:36Z
dc.date.issued 2012-12-12
dc.description.abstract A stereoselective methodology was developed for the construction of C-spiro-glycosides in two steps involving bromonium ion activated solvolytic ring opening of sugar derived 1,2-cyclopropanecarboxylates followed by a one-pot dehydrohalogenation, intramolecular hetero-Michael addition (IHMA) and ester hydrolysis. The obtained spirocyclic lactols were further converted to enantiomerically pure spirolactones. © 2012 The Royal Society of Chemistry.
dc.identifier.citation Chemical Communications. v.48(5)
dc.identifier.issn 13597345
dc.identifier.uri 10.1039/c1cc16417a
dc.identifier.uri http://xlink.rsc.org/?DOI=C1CC16417A
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11265
dc.title Stereoselective synthesis of sugar fused β-disubstituted γ-butyro-lactones: C-spiro-glycosides from 1,2-cyclopropanecarboxylated sugars
dc.type Journal. Article
dspace.entity.type
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