The Allyl Group for Protection in Carbohydrate Chemistry. Part 20. Synthesis of 1L-1-O-Methyl-myo-inositol by Resolution of (+/-)-1,2,4-Tri-O-benzyl-myo-inositol

DOI: 10.1039/P19870001757

Source and publish data:

Journal of the Chemical Society. Perkin transactions I p. 1757 - 1762 (1987)

Update date:2022-08-02

Topics: Resolution Protection (+/-)-1,2,4-tri-O-benzyl-myo-inositol Allyl group Carbohydrate chemistry

Authors:

Gigg, Jill

Gigg, Roy

Payne, Sheila

Conant, Robert

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Article abstract of DOI:10.1039/P19870001757

Racemic 1,2,4-tri-O-benzyl-myo-inositol was prepared by two new routes from (+/-)-1,4-di-O-benzyl-5,6-O-isopropylidine-myo-inositol, one route involving the crystalline intermediate (+/-)-1-O-allyl-3,6-di-O-benzyl-4,5-O-isopropylidine-myo-inositol.Oxidati

Full text of DOI:10.1039/P19870001757

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