“…invent truly new and different glycosylation strategies that will not require a bimolecular reaction to occur between a developing oxocarbonium ion and a sterically hindered lowly nucleophilic alchol…” This challenge by F. Barresi and O. Hindsgaul to all carbohydrate chemists now has a novel reply, which can be described by the sequence in Equation (a)
The Cycloaddition Way to Glycosyl Transfer / G. Capozzi; A. Dios; R. Franck; A. Geer; C. Marzabadi; S. Menichetti; C. Nativi; M. Tamarez. - In: ANGEWANDTE CHEMIE. INTERNATIONAL EDITION IN ENGLISH. - ISSN 0570-0833. - STAMPA. - 35:(1996), pp. 777-779. [10.1002/anie.199607771]
The Cycloaddition Way to Glycosyl Transfer
CAPOZZI, GIUSEPPE;MENICHETTI, STEFANO;NATIVI, CRISTINA;
1996
Abstract
“…invent truly new and different glycosylation strategies that will not require a bimolecular reaction to occur between a developing oxocarbonium ion and a sterically hindered lowly nucleophilic alchol…” This challenge by F. Barresi and O. Hindsgaul to all carbohydrate chemists now has a novel reply, which can be described by the sequence in Equation (a)
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