A short time isomerisation for the synthesis of 3-ylideneoxindoles from Morita-Baylis-Hillman adduct of isatin derivatives with 1-hexyn-3-ol using FeCl3 and K-10 clay
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference43 articles.
1. Phytoalexins from Thlaspi arvense, a wild crucifer resistant to virulent Leptosphaeria maculans: structures, syntheses and antifungal activity
2. Synthesis and evaluation of 3-ylideneoxindole acetamides as potent anticancer agents
3. Synthesis and biological evaluation of 2-indolinone derivatives as potential antitumor agents
4. Novel Oxindole Based Sensitizers: Synthesis and Application in Dye-Sensitized Solar Cells
5. Part I: Diastereoselective Reactions Involving β-Mono- and β,β′-Disubstituted Alkylidene Oxindoles: Pondering Alkene Geometry
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Eco-friendly K-10 Clay-Mediated [3 + 3] Spiroannulation of Morita–Baylis–Hillman Adduct of Isatin with Anthracene: Synthesis of Green Fluorophore Compounds;ACS Omega;2023-12-20
2. Diastereoselective Construction of Tetrahydro-Dispiro[indolinone-3,2′-pyran-5′,4″-pyrazolone] Scaffolds via an Oxa-Michael Cascade [4 + 2] Annulation Reaction;The Journal of Organic Chemistry;2022-09-16
3. Allylic arylative isomerisation of Morita-Baylis-Hillman adduct of isatin derivatives with arenes using FeCl3 and K-10 clay;Results in Chemistry;2022-01
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