Intramolecular C-arylation of 2,3,5-tri-O-benzyl- and 2,3,5-tri-O-(3-methylbenzyl)-pentofuranose derivatives.

DOI: 10.1016/S0008-6215(00)90888-7

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Carbohydrate research p. 211 - 222 (1987)

Update date:2022-08-04

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Article abstract of DOI:10.1016/S0008-6215(00)90888-7

Upon treatment with tin(IV) chloride, 1-O-acetyl-2,3,5-tri-O-benzyl- and 1-O-acetyl-2,3,5-tri-O-(3-methylbenzyl)pentofuranose (D-ribo, L-arabino) undergo intramolecular Friedel-Crafts alkylation of the aromatic substituent at O-2 to give unusual internal

Full text of DOI:10.1016/S0008-6215(00)90888-7

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Intramolecular C-arylation of 2,3,5-tri-O-benzyl- and 2,3,5-tri-O-(3-methylbenzyl)-pentofuranose derivatives.

DOI: 10.1016/S0008-6215(00)90888-7

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0008-6215(00)90888-7

Full text of DOI:10.1016/S0008-6215(00)90888-7

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