Expeditious Metal-Free Access to Functionalized Polycyclic Acetals under Mild Aqueous Conditions

dc.contributor.authorKasare, S.
dc.contributor.authorBankar, S.K.
dc.contributor.authorRamasastry, S.S.V.
dc.date.accessioned2020-12-09T06:58:11Z
dc.date.available2020-12-09T06:58:11Z
dc.date.issued2014
dc.description.abstractA facile approach for the synthesis of furopyrans and bicyclic bisacetals under mild aqueous conditions is described. This potentially green, diversity oriented approach involves cascade Michael addition and cycloacetalization of pyranones and 1,3-dicarbonyls. An interesting switch in the product class was observed depending on the type of pyranone employed. Products of type I and II obtained herein are an integral part of several bioactive natural products and medicinally interesting compounds. © 2014 American Chemical Society.en_US
dc.identifier.citationOrganic Letters,16(16), pp.4284-4287.en_US
dc.identifier.otherhttps://doi.org/10.1021/ol501986f
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/ol501986f
dc.identifier.urihttp://hdl.handle.net/123456789/2879
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectSodium dodecyl sulfateen_US
dc.subjectOrganic compoundsen_US
dc.subjectChemical reactionsen_US
dc.subjectPharmaceuticalsen_US
dc.titleExpeditious Metal-Free Access to Functionalized Polycyclic Acetals under Mild Aqueous Conditionsen_US
dc.typeArticleen_US

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