Baylis-Hillman acetates in organic synthesis: Convenient one-pot synthesis of α-carboline framework - A concise synthesis of neocryptolepine

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Mallikarjuna Reddy, Daggula
dc.date.accessioned 2022-03-27T09:01:19Z
dc.date.available 2022-03-27T09:01:19Z
dc.date.issued 2012-11-28
dc.description.abstract A convenient, facile, and one-pot methodology for the synthesis of α-carbolines from Baylis-Hillman (BH) acetates, involving three steps (reactions), (1) mono alkylation of 2-nitroarylacetonitriles with BH-acetates, (2) reduction of nitro group into amino group using Fe/AcOH and (3) formation of two (five and six membered) rings, is presented. This methodology is successfully applied to the synthesis of bioactive alkaloid neocryptolepine. © 2012 The Royal Society of Chemistry.
dc.identifier.citation Organic and Biomolecular Chemistry. v.10(44)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/c2ob26339d
dc.identifier.uri http://xlink.rsc.org/?DOI=c2ob26339d
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12280
dc.title Baylis-Hillman acetates in organic synthesis: Convenient one-pot synthesis of α-carboline framework - A concise synthesis of neocryptolepine
dc.type Journal. Article
dspace.entity.type
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