An Orchestrated Unsymmetrical Annulation Episode of C(sp < sup > 2 < /sup > )-H Bonds with Alkynes and Quinones: Access to Spiro-isoquinolones

dc.contributor.author Mukherjee, Kallol
dc.contributor.author Shankar, Majji
dc.contributor.author Ghosh, Koushik
dc.contributor.author Sahoo, Akhila K.
dc.date.accessioned 2022-03-27T09:50:38Z
dc.date.available 2022-03-27T09:50:38Z
dc.date.issued 2018-04-06
dc.description.abstract A nontrivial Ru-catalyzed one-pot sequential oxidative coupling of a (hetero)arene/vinylic/chromene system with alkyne and quinone is presented; the methyl phenyl sulfoximine (MPS) directing group is vital. This cyclization forms four (two C-C and two C-N) bonds in a single operation and produces unusual spiro-fused-isoquinolones with a broad scope. The release of phenyl methyl sulfoxide makes the MPS group transformable. A deuterium scrambling study sheds light on the reaction path.
dc.identifier.citation Organic Letters. v.20(7)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/acs.orglett.8b00468
dc.identifier.uri https://pubs.acs.org/doi/10.1021/acs.orglett.8b00468
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13363
dc.title An Orchestrated Unsymmetrical Annulation Episode of C(sp < sup > 2 < /sup > )-H Bonds with Alkynes and Quinones: Access to Spiro-isoquinolones
dc.type Journal. Article
dspace.entity.type
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