Baylis-Hillman bromides as a source of 1,3-dipoles: Sterically directed synthesis of oxindole-fused spirooxirane and spirodihydrofuran frameworks

dc.contributor.author Basavaiah, Deevi
dc.contributor.author Badsara, Satpal Singh
dc.contributor.author Sahu, Bharat Chandra
dc.date.accessioned 2022-03-27T09:01:10Z
dc.date.available 2022-03-27T09:01:10Z
dc.date.issued 2013-02-25
dc.description.abstract Poles apart: The sterically directed [3+2] cycloaddition reactions of dipoles that were generated from Baylis-Hillman bromides with isatin dipolarophiles provided a facile synthetic route to spirodihydrofuran oxindoles and spiroepoxy oxindoles (see scheme). a)-c) Me2S, Cs 2CO3, DMF, 15-20 °C, N2, 8 h. EWG: a) CO2Me (Z), b) CO2Me, and c) CN (E). Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.identifier.citation Chemistry - A European Journal. v.19(9)
dc.identifier.issn 09476539
dc.identifier.uri 10.1002/chem.201203756
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/chem.201203756
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12276
dc.subject cycloaddition
dc.subject dipoles
dc.subject fused-ring systems
dc.subject heterocycles
dc.subject spiro compounds
dc.title Baylis-Hillman bromides as a source of 1,3-dipoles: Sterically directed synthesis of oxindole-fused spirooxirane and spirodihydrofuran frameworks
dc.type Journal. Article
dspace.entity.type
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