The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: A facile synthesis of functionalized tri-/tetracyclic frameworks containing azocine moiety

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Aravindu, Kunche
dc.date.accessioned 2022-03-27T09:01:55Z
dc.date.available 2022-03-27T09:01:55Z
dc.date.issued 2007-06-21
dc.description.abstract The Baylis-Hillman acetates have been conveniently transformed into tri-/tetracyclic heterocyclic frameworks containing an important azocine moiety via one-pot multistep protocol involving alkylation, reduction, and cyclization sequence. © 2007 American Chemical Society.
dc.identifier.citation Organic Letters. v.9(13)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/ol070380u
dc.identifier.uri https://pubs.acs.org/doi/10.1021/ol070380u
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12298
dc.title The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: A facile synthesis of functionalized tri-/tetracyclic frameworks containing azocine moiety
dc.type Journal. Article
dspace.entity.type
Files
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Plain Text
Description: