Active Cobalt Catalyst for the Cleavage of Benzyl Ether
Author:
Affiliation:
1. The State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, P. R. China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo2018284
Reference23 articles.
1. Greene, T. W.; Wuts, P. G. M.Greene’s Protective Groups in Organic Synthesis,4th ed.John Wiley & Sons:Hoboken, NJ, 2007; Chapter 2, pp102.
2. Selective hydrogenolysis of benzyl ethers in the presence of benzylidene acetals with Raney nickel
3. Removal of Benzyl Protecting Groups from Solid-Supported Compounds by Hydrogenolysis Using Palladium Nanoparticles
4. Total synthesis of an enantiomeric pair of FR900482. 2. Syntheses of the aromatic and the optically active aliphatic segments
5. On the selectivity of deprotection of benzyl, mpm (4-methoxybenzyl) and dmpm (3,4-dimethoxybenzyl) protecting groups for hydroxy functions
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