Transformable Sulfoximine Assisted One-Pot Double Annulation of Vinylic C-H Bonds with Unactivated Alkynes

dc.contributor.author Shankar, Majji
dc.contributor.author Guntreddi, Tirumaleswararao
dc.contributor.author Ramesh, E.
dc.contributor.author Sahoo, Akhila K.
dc.date.accessioned 2022-03-27T09:52:38Z
dc.date.available 2022-03-27T09:52:38Z
dc.date.issued 2017-10-20
dc.description.abstract The methylphenyl sulfoximine (MPS) directing group (DG) successfully promotes the one-pot double annulation of acrylic acids with alkynes under Ru catalysis, which is unprecedented. Diverse arrays of pyrido-fused-isoquinolinone skeletons are fabricated from acrylamides, creating two C-C and two C-N bonds in a single operation. The unsymmetrical annulation with two distinct alkynes is presented. The recovery of methylphenyl sulfoxide, a precursor of MPS, validates the synthetic adaptability of transformable-DG (TfDG) in C-H activation.
dc.identifier.citation Organic Letters. v.19(20)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/acs.orglett.7b02824
dc.identifier.uri https://pubs.acs.org/doi/10.1021/acs.orglett.7b02824
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13396
dc.title Transformable Sulfoximine Assisted One-Pot Double Annulation of Vinylic C-H Bonds with Unactivated Alkynes
dc.type Journal. Article
dspace.entity.type
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