Papulacandins and chaetiacandin: a stereoselective route to their basic skeleton by a palladium-mediated arylation of 4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-1-tributylstannyl-D-glucal

DOI: 10.1016/0008-6215(92)80014-R

Source and publish data:

Carbohydrate Research p. 157 - 168 (1992)

Update date:2022-08-04

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Authors:

Dubois, Eric

Beau, Jean-Marie

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Article abstract of DOI:10.1016/0008-6215(92)80014-R

Palladium(0)-catalysed coupling of 1,5-anhydro-4,6-O-benzylidene-3-O-tert-butyldimethylsilyl-2-deoxy-1-tributylstannyl-D-arabino-hex-1-enitol (7) with 3,5-dibenzyloxy-2-bromobenzyl alcohol gave 1,1²-anhydro-4,6-O-benzylidene-3-O-tert-butyldimet

Full text of DOI:10.1016/0008-6215(92)80014-R

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