Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/3839
Title: Base-enabled Access to Diastereoselective Spirofuran Oxindoles and γ-functionalized Allenoates
Authors: Basavaraja, D
Ajay Krishna, M S
Krishnan, J
Athira, C S
Amrutha, R R
Suresh, E
Sasidhar, B S
Issue Date: 2021
Publisher: Royal Society of Chemistry
Citation: Chemical Communications; 57(14):1746-1749
Abstract: Base assisted divergent reactivity of isatins and allenoates has been achieved, which afforded diastereoselective spirofuran oxindoles and γ-functionalized allenoates. The DBU mediated Morita–Baylis–Hillman (MBH) reaction followed by the cascade annulation through the stabilized β-ammonium enolate intermediate led to the spiro-framework, wherein DABCO furnished the γ-functionalized allenoates. The protocol offers access to biologically relevant functionalized oxindole scaffolds with an excellent substrate scope under mild reaction conditions.
URI: https://pubs.rsc.org/en/content/articlelanding/2021/cc/d0cc07715a#!divAbstract
http://hdl.handle.net/123456789/3839
Appears in Collections:2021

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