A mild copper catalyzed method for the selective deprotection of aryl allyl ethers
Author:
Funder
GSK/EPSRC
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference36 articles.
1. Greene’s Protective Groups in Organic Synthesis;Wuts,2006
2. Facile and selective cleavage of allyl ethers, amines and esters using polymethylhydrosiloxane–ZnCl 2 /Pd(PPh 3 ) 4
3. Cleavage of allyloxycarbonyl protecting group from oxygen and nitrogen under mild conditions by nickel carbonyl
4. Palladium charcoal-catalyzed deprotection of O-allylphenols
5. A Mild Deprotection Strategy for Allyl-Protecting Groups and Its Implications in Sequence Specific Dendrimer Synthesis
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1. Efficient O-deallylation triggered by cobalt hydride-catalyzed oxidative hydrofunctionalization;Green Synthesis and Catalysis;2023-02
2. Iodine‐DMSO catalyzed chemoselective oxidative aromatization and deallylation, nondeallylation of aryl allyl ether of tetrahydro‐ β ‐carboline;Journal of Heterocyclic Chemistry;2021-04-12
3. Nickel Hydride Catalyzed Cleavage of Allyl Ethers Induced by Isomerization;Synlett;2021-01-22
4. Advances in Deallylation;Chinese Journal of Organic Chemistry;2021
5. A mild and practical method for deprotection of aryl methyl/benzyl/allyl ethers with HPPh2 and tBuOK;Organic & Biomolecular Chemistry;2021
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