Water Promoted Sulfa-Michael Addition Reaction using Hydrazones as Sulfonyl Transfer Reagent

dc.contributor.authorShagun
dc.contributor.supervisorTyagi, Vikas
dc.date.accessioned2019-09-10T11:01:34Z
dc.date.available2019-09-10T11:01:34Z
dc.date.issued2019-09-10
dc.descriptionM.Sc Thesisen_US
dc.description.abstractA catalyst free, facile and green route has been identified for the synthesis of -keto sulfones through highly efficient water promoted sulfa-Michael addition. Sulfonyl hydrazones have been exploited as magnificent sulfonyl anion surrogate in presence of water with enones and with other α, β unsaturated alkenes for the synthesis of functionalized sulfones. To test the feasibility of the reaction a number of substituent has been screened and to our delight we got good to excellent yield with all substitutions. Further, to check the scalability of the transformation a reaction was set-up with one gm scale of starting materials and the higher yield of product proves that this transformation might be useful at industrial scale.en_US
dc.identifier.urihttp://hdl.handle.net/10266/5757
dc.language.isoenen_US
dc.subjectWateren_US
dc.subjectN-tolge dydrozoneen_US
dc.subjectSulfaMichael Reactionen_US
dc.subjectr-Keto Sulfonesen_US
dc.subjectr-nitrite sulfones computational Studyen_US
dc.titleWater Promoted Sulfa-Michael Addition Reaction using Hydrazones as Sulfonyl Transfer Reagenten_US
dc.typeThesisen_US

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