Improvements in the regioselectivity of alkylation reactions of stannylene acetals

Article abstract of DOI:10.1080/07328309608005428

The regioselectivity of benzylation of stannylene acetals of trans-diols on pyranose rings is improved by performing the reaction in benzyl bromide, for instance, for methyl 4,6-O-benzylidene-2,3-O-dibutylstannylene-α-D-glucopyranoside, the ratio of 2-O-b

Full text of DOI:10.1080/07328309608005428

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Journal of Carbohydrate Chemistry
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Improvements in the Regioselectivity
of Alkylation Reactions of Stannylene
Acetals
Huiping Qin a & T. Bruce Grindley a
a Department of Chemistry, Dalhousie University, Halifax, N.S.,
Canada, B3H 4J3
Version of record first published: 22 Aug 2006.
To cite this article: Huiping Qin & T. Bruce Grindley (1996): Improvements in the Regioselectivity of
Alkylation Reactions of Stannylene Acetals, Journal of Carbohydrate Chemistry, 15:1, 95-108
To link to this article: http://dx.doi.org/10.1080/07328309608005428
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