The Baylis-Hillman adducts as valuable source for one-pot multi-step synthesis: A facile synthesis of substituted piperidin-2-ones

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Reddy, Raju Jannapu
dc.contributor.author Lenin, Dandamudi V.
dc.date.accessioned 2022-03-27T09:01:32Z
dc.date.available 2022-03-27T09:01:32Z
dc.date.issued 2010-06-01
dc.description.abstract A facile, convenient, and one-pot multi-step synthesis of substituted piperidin-2-ones from the Baylis - Hillman alcohols derived from various aldehydes and acrylonitrile, involving Johnson - Claisen rearrangement, reduction of an α,β-unsaturated nitrile moiety into the saturated amine-skeleton, followed by cyclization, in an operationally simple procedure, is described. © 2010 Verlag Helvetica Chimica Acta AG.
dc.identifier.citation Helvetica Chimica Acta. v.93(6)
dc.identifier.issn 0018019X
dc.identifier.uri 10.1002/hlca.200900352
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/hlca.200900352
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12287
dc.title The Baylis-Hillman adducts as valuable source for one-pot multi-step synthesis: A facile synthesis of substituted piperidin-2-ones
dc.type Journal. Article
dspace.entity.type
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