| Literature DB >> 28375019 |
Robert A Green1, Katherine E Jolley1, Azzam A M Al-Hadedi1, Derek Pletcher1, David C Harrowven1, Oscar De Frutos2, Carlos Mateos2, David J Klauber3, Juan A Rincón2, Richard C D Brown1.
Abstract
Electrochemical deprotection of p-methoxybenzyl (PMB) ethers was performed in an undivided electrochemical flow reactor in MeOH solution, leading to the unmasked alcohol and p-methoxybenzaldehyde dimethyl acetal as a byproduct. The electrochemical method removes the need for chemical oxidants, and added electrolyte (BF4NEt4) can be recovered and reused. The method was applied to 17 substrates with high conversions in a single pass, yields up to 92%, and up to 7.5 g h-1 productivity. The PMB protecting group was also selectively removed in the presence of some other common alcohol protecting groups.Entities:
Year: 2017 PMID: 28375019 DOI: 10.1021/acs.orglett.7b00641
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005