Phosphine- and water-promoted pentannulative aldol reaction†

dc.contributor.authorSatpathi, B.
dc.contributor.authorDutta, L.
dc.contributor.authorRamasastry, S.S.V.
dc.date.accessioned2020-11-27T10:51:33Z
dc.date.available2020-11-27T10:51:33Z
dc.date.issued2019
dc.description.abstractHerein, an efficient metal-free intramolecular aldol reaction for the synthesis of an unusual class of cyclopentanoids is described. The reaction of α-substituted dienones tethered with ketones in the presence of tributylphosphine and water provided aldols. The role of water was realised to be crucial for this transformation. Furthermore, isotopic labeling experiments provided vital information about the reaction mechanism.en_US
dc.identifier.citationOrganic and Biomolecular Chemistry, 17(6),pp.1547-1551.en_US
dc.identifier.otherhttps://doi.org/10.1039/C8OB03106A
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2019/ob/c8ob03106a#!divAbstract
dc.identifier.urihttp://hdl.handle.net/123456789/2346
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectMetal-freeen_US
dc.subjectReactionen_US
dc.subjectEfficienten_US
dc.titlePhosphine- and water-promoted pentannulative aldol reaction†en_US
dc.typeArticleen_US

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