Selective demethylation and debenzylation of aryl ethers by magnesium iodide under solvent-free conditions and its application to the total synthesis of natural products.

Kai Bao, Aixue Fan, Yi Dai, Liang Zhang, Weige Zhang, Maosheng Cheng, Xinsheng Yao

Journal: Organic & biomolecular chemistry 2010;7(24):5084-90

PMID: 20024102

Abstract

An efficient selective demethylation and debenzylation method for aryl methyl/benzyl ethers using magnesium iodide under solvent-free conditions has been developed and applied to the synthesis of natural flavone and biphenyl glycosides. A variety of functional groups including glycoside were tolerated under the reaction conditions. Experimental results indicated that the removal of an O-benzyl group was easier than that of an O-methyl group, regardless of wherever they were meta or para to the carbonyl. Thus selective debenzylation can be achieved for substrates bearing both benzyloxy and methoxy groups.

Address: School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang, PR China.

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