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P-Anisyloxymethyl ethers,

Methoxyphenoxy)methyl Ether (p-AOM-OR), (p-Anisyloxymethyl Ether) ROCH2OC6H4-4 OCH3... [Pg.24]

The p-anisyloxymethyl group520 (abbreviated AOM) played an important role in the synthesis of Calicheamicinone reported by Clive and co-workers.521 Its removal from the sensitive multifunctional substrate 285 1 [Scheme 4.285] was accomplished with CAN in a mixture of pyridine, methanol and water. The excellent yield (89%) attests to the mildness of the conditions. Attempts to apply the same conditions to the deprotection of an AOM group from 286 1 [Scheme 4.286]522 failed but the deprotection was successful if it was conducted in the presence of 2,6-pyridinedicarboxylic acid N-oxide — conditions previously used to convert a phenol methyl ether to a quinone.523 AOM ethers undergo easy reductive cleavage to the corresponding methyl ethers with borane in toluene — a reaction that could have synthetic value when simple O-methylation procedures fail. [Pg.312]


See other pages where P-Anisyloxymethyl ethers, is mentioned: [Pg.234]    [Pg.45]    [Pg.19]    [Pg.234]    [Pg.45]    [Pg.19]    [Pg.38]   


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P- ethers

P-anisyloxymethyl

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