Concise total synthesis of cytotoxic natural products (+) and (-)-muricatacin

dc.contributor.author Yaragorla, Srinivasarao
dc.contributor.author Muthyala, Ramaiah
dc.date.accessioned 2022-03-27T08:50:19Z
dc.date.available 2022-03-27T08:50:19Z
dc.date.issued 2010-08-01
dc.description.abstract A short and efficient total synthesis of antitumor natural products (+) and (-)-muricatacin is described in four steps with an overall yield of 47%. The key reactions involved in the synthesis are Ph3P mediated isomerization and asymmetric dihydroxylation. © ARKAT USA, Inc.
dc.identifier.citation Arkivoc. v.2010(10)
dc.identifier.issn 1551-7012
dc.identifier.uri 10.3998/ark.5550190.0011.a15
dc.identifier.uri https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.0011.a15
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11908
dc.subject Butyrolactone
dc.subject Dihydroxylation
dc.subject Muricatacin
dc.subject Natural product
dc.subject Total synthesis
dc.subject Triphenylphosphine mediated isomerization
dc.title Concise total synthesis of cytotoxic natural products (+) and (-)-muricatacin
dc.type Journal. Article
dspace.entity.type
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