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 |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
Base-enabled access to diastereoselective spirofuran oxindoles_BasavarajaD_Chemical Communication.pdf Restricted Access | 3.14 MB | Adobe PDF | View/Open Request a copy |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.