Multiple and long-range participation of benzyl groups in intramolecular C-arylation reactions of benzylated glycosides
The intrinsic reactivity of furanosides bearing activated O-benzyl substituents (3-methoxybenzyl), in the presence of bidentate Lewis acids such as tin(IV) chloride, was explored. These glycosides were found to exhibit extremely interesting chemical properties. Thus, with three reactive substituents...
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Veröffentlicht in: | Carbohydrate research 1990-07, Vol.202, p.49-66 |
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