A novel route to synthesize lavendamycin analogues through an A < sup > 3 < /sup > coupling reaction

dc.contributor.author Ramesh, Subburethinam
dc.contributor.author Nagarajan, Rajagopal
dc.date.accessioned 2022-03-27T08:40:06Z
dc.date.available 2022-03-27T08:40:06Z
dc.date.issued 2013-06-17
dc.description.abstract A convergent synthesis of lavendamycin analogues has been accomplished by using A3 coupling reaction between carboline aldehydes, anilines, and phenylacetylenes. Our approach features the use of the ionic liquids as an environmentally benign solvent medium and synthesis of lavendamycin analogues with diverse substitution pattern. Additionally, the formation of α-dihydropyrido-β-carboline was observed during the reaction of α-formyl-β-carboline, aniline, and ethylpropiolate. © 2013 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron. v.69(24)
dc.identifier.issn 00404020
dc.identifier.uri 10.1016/j.tet.2013.04.074
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040402013006121
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11431
dc.subject A coupling 3
dc.subject Ionic liquid Quinoline
dc.subject Lavendamycin
dc.subject MCR
dc.title A novel route to synthesize lavendamycin analogues through an A < sup > 3 < /sup > coupling reaction
dc.type Journal. Article
dspace.entity.type
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