Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2766
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dc.contributor.authorBankar, S.K.-
dc.contributor.authorShirke, R.P.-
dc.contributor.authorRamasastry, S.S.V.-
dc.date.accessioned2020-12-07T10:33:12Z-
dc.date.available2020-12-07T10:33:12Z-
dc.date.issued2015-
dc.identifier.citationAdvanced Synthesis and Catalysis, 357 (14-15)en_US
dc.identifier.other10.1002/adsc.201500505-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/adsc.201500505-
dc.identifier.urihttp://hdl.handle.net/123456789/2766-
dc.description.abstractAn efficient diversity‐oriented approach for the synthesis of previously unknown di‐, tri‐, tetra‐ and spirocyclic pyrano‐1,4‐dioxinones, pyrano‐1,4‐dithiinones and pyrano‐1,4‐oxathiinones from readily available starting compounds has been described. Cascade Michael addition–cycloacetalisation of acetoxy‐, alkoxy‐, and aryloxypyranones and 1,2‐dinucleophiles under mild Lewis acidic conditions provides a direct access to oxygen and sulfur‐containing complex heterocycles. Mechanistic aspects of the cascade process were elucidated in light of experimental facts. The methodology described herein shows high promise for the synthesis of several bioactive natural products as well as pharmaceutically important compounds.en_US
dc.language.isoen_USen_US
dc.publisherWiley-VCH Verlagen_US
dc.subjectcascade reactionsen_US
dc.subjectheterocyclesen_US
dc.subjectLewis acidsen_US
dc.subjectnatural productsen_US
dc.subjectpyranonesen_US
dc.titleSynthesis of O,S-Containing Polycycles via One-Pot Michael Addition-Cycloacetalisation Cascadeen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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