Title:
Applications of dithioacetals in ester synthesis

dc.contributor.authorAshish Kumar Tewari
dc.contributor.authorPriyanka Srivastava
dc.date.accessioned2026-02-07T04:54:28Z
dc.date.issued2009
dc.description.abstractThe α-oxoketene dithioacetals are simple synthetic intermediates widely utilized and implicated for the synthesis of a variety of heterocyclic compounds other than alicyclic and aromatic compounds. They act as 1,3-electrophilic three-carbon synthons. The -oxoketene dithioacetal of pyrazolone derivatives can be efficiently converted through a base-catalyzed alcoholysis into the corresponding ester in a single one-step reaction with good yield of pure products. In this article, we summarize recent direct conversion of α-oxoketene dithioacetals to highly desirable esters. The overall process is an example of intramolecular rearrangement of bonds. Characterization and identification of all synthesized compounds were assigned through 1H NMR and mass spectroscopy.
dc.identifier.doi10.1080/00397910802654641
dc.identifier.issn15322432
dc.identifier.urihttps://doi.org/10.1080/00397910802654641
dc.identifier.urihttps://dl.bhu.ac.in/bhuir/handle/123456789/21139
dc.subjectα-oxoketene dithioacetal
dc.subjectAlcoholysis
dc.subjectCyclocondensation
dc.subjectS,O-Acetal
dc.subjectSynthons
dc.subjectThiomethyl
dc.titleApplications of dithioacetals in ester synthesis
dc.typePublication
dspace.entity.typeArticle

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