Total synthesis of (±)-grimaldone, epigrimaldone and α-cuparenones

dc.contributor.author Srikrishna, A.
dc.contributor.author Ramachary, D. B.
dc.date.accessioned 2022-03-27T09:42:17Z
dc.date.available 2022-03-27T09:42:17Z
dc.date.issued 2006-05-01
dc.description.abstract Total synthesis of (±)-grimaldone, epigrimaldone and α-cuparenone has been described. A combination of orthoester Claisen rearrangement, an acid catalysed rearrangement of a diazoketone for the generation of bicyclo[4.2.1]nonanedione, a retro-Claisen condensation and an intramolecular diazoketone cyclopropanation reaction have been employed for the construction of three contiguous quaternary atoms present in grimaldone and epigrimaldones.
dc.identifier.citation Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. v.45(5)
dc.identifier.issn 03764699
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13216
dc.subject α-cuparenone
dc.subject Claisen rearrangement
dc.subject Cyclopropanation reaction
dc.subject Diazoketone
dc.subject Epigrimaldone
dc.subject Grimaldone
dc.subject Retro-Claisen condensation
dc.title Total synthesis of (±)-grimaldone, epigrimaldone and α-cuparenones
dc.type Journal. Article
dspace.entity.type
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