Catalytic Ynone-Amidine Formal [4 + 2]-Cycloaddition for the Regioselective Synthesis of Tricyclic Azepines

dc.contributor.author Reddy, T. Prabhakar
dc.contributor.author Gujral, Jagjeet
dc.contributor.author Roy, Pritam
dc.contributor.author Ramachary, Dhevalapally B.
dc.date.accessioned 2022-03-27T09:36:39Z
dc.date.available 2022-03-27T09:36:39Z
dc.date.issued 2020-12-18
dc.description.abstract A Ca(OTf)2- and self-promoted ynone-amidine atom-economic formal [4 + 2]-cycloaddition of various ynones with amidines is reported for the construction of highly functionalized tricyclic azepines. High reaction rate, ease of operation, and high product selectivity with wide substrate scope are the key advantages of the present annulation protocol.
dc.identifier.citation Organic Letters. v.22(24)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/acs.orglett.0c03711
dc.identifier.uri https://pubs.acs.org/doi/10.1021/acs.orglett.0c03711
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13111
dc.title Catalytic Ynone-Amidine Formal [4 + 2]-Cycloaddition for the Regioselective Synthesis of Tricyclic Azepines
dc.type Journal. Article
dspace.entity.type
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