A novel type of spiroketalisation on pyranoses

DOI: 10.1016/0008-6215(92)84174-Q

Source and publish data:

Carbohydrate Research p. 375 - 379 (1991)

Update date:2022-07-29

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Authors:

Haudrechy

Sinay Sinay

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Article abstract of DOI:10.1016/0008-6215(92)84174-Q

2,6-Anhydro-3,4,5,7-tetra-O-benzyl-1-deoxy-D-gluco-hept-1-enitol (3) was converted into allyl 3,4,5,7-tetra-O-benzyl-1-deoxy-1-iodo-α-D-gluco-2-heptulopyranoside (4) upon addition of allylic alcohol in the presence of N-iodosuccinimide. Treatment of 4 wit

Full text of DOI:10.1016/0008-6215(92)84174-Q

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Product name:allyl 3,4,5,7-tetra-O-benzyl-1-deoxy-1-iodo-α-D-gluco-2-heptulopyranoside

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