A new entry to polycyclic indole derivatives via intramolecular imino Diels-Alder reaction: Observation of unexpected reaction

dc.contributor.author Gaddam, Vikram
dc.contributor.author Nagarajan, Rajagopal
dc.date.accessioned 2022-03-27T08:40:46Z
dc.date.available 2022-03-27T08:40:46Z
dc.date.issued 2007-04-27
dc.description.abstract (Chemical Equation Presented) A new, efficient, and highly diastereoselective synthesis of polycyclic indole derivatives through intramolecular imino Diels - Alder reaction of aminoanthraquinone with N-prenylated indole-2-carboxaldehydes in the presence of 20 mol % of triphenylphosphonium perchlorate (TPPP) is reported with extremely high cis selectivity in good yield. © 2007 American Chemical Society.
dc.identifier.citation Journal of Organic Chemistry. v.72(9)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo062321k
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jo062321k
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11469
dc.title A new entry to polycyclic indole derivatives via intramolecular imino Diels-Alder reaction: Observation of unexpected reaction
dc.type Journal. Article
dspace.entity.type
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