The preparation and phosphorylation of 2,5- and 1D-2,6-di-O-benzyl-myo-inositol

DOI: 10.1016/S0008-6215(00)90549-4

Source and publish data:

Carbohydrate Research p. 65 - 79 (1992)

Update date:2022-08-03

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Authors:

Desai Desai

Gigg Gigg

Payne Payne

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Article abstract of DOI:10.1016/S0008-6215(00)90549-4

1,3,4,6-Tetra-O-allyl-myo-inositol was converted into the 2,5-di-O-benzyl- and 2,5-di-O-p-methoxybenzyl ethers, and the products were deallylated to give the 2,5-di-O-benzyl (and p-methoxybenzyl) ethers of myo-inositol, which were converted into the mono-

Full text of DOI:10.1016/S0008-6215(00)90549-4

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