Total synthesis of (±)-β-microbiotene, (±)-microbiotol, (±)-cyclocuparanol and (±)-β-cuparenones

dc.contributor.author Srikrishna, A.
dc.contributor.author Ramachary, D. B.
dc.date.accessioned 2022-03-27T09:41:57Z
dc.date.available 2022-03-27T09:41:57Z
dc.date.issued 2007-05-01
dc.description.abstract Total synthesis of (±)-β-microbiotene, (±)-microbiotol, (±)-cyclocuparanol and their epimers along with (±)-β- 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 cyclocuparanes.
dc.identifier.citation Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry. v.46(5)
dc.identifier.issn 03764699
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13210
dc.subject Cuparenes
dc.subject Cyclocuparanes
dc.subject Cyclopropanation
dc.subject Diazo ketones
dc.subject Rearrangement
dc.subject Sesquiterpene synthesis
dc.title Total synthesis of (±)-β-microbiotene, (±)-microbiotol, (±)-cyclocuparanol and (±)-β-cuparenones
dc.type Journal. Article
dspace.entity.type
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