
doi: 10.1271/bbb.90242
pmid: 19809189
The first total syntheses of benzophenone glucopyranosides reported from Phaleria macrocarpa and related benzophenone glucopyranosides were successfully carried out. The alkoxy groups present ortho to the carbonyl group in polyalkoxybenzophenones were selectively deprotected by AlCl(3)-PhNMe(2) in high yields, leaving other alkoxy groups unaffected. It was concluded in the current synthetic study that all the reported benzophenone glucopyranosides possessed the same structure as 2,4',6-trihydroxy-4-methoxybenzophenone 2-O-beta-D-glucopyranoside.
Benzophenones, Structure-Activity Relationship, Magnetic Resonance Spectroscopy, AlCl<SUB>3</SUB>–PhNMe<SUB>2</SUB>, Thymelaeaceae, selective dealkylation, Glycosides, benzophenone glucopyranoside, <I>Phaleria macrocarpa</I>
Benzophenones, Structure-Activity Relationship, Magnetic Resonance Spectroscopy, AlCl<SUB>3</SUB>–PhNMe<SUB>2</SUB>, Thymelaeaceae, selective dealkylation, Glycosides, benzophenone glucopyranoside, <I>Phaleria macrocarpa</I>
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