| Literature DB >> 21078510 |
Iain A S Smellie1, Andreas Fromm, Stephen A Moggach, R Michael Paton.
Abstract
The first examples of 2-pyranosylperimidines are reported. The β-d-glucopyranosyl nitrile oxide 5, generated by base-induced dehydrochlorination of the hydroximoyl chloride 4, reacted with 1,8-diaminonaphthalene to afford the 2-(β-d-glucopyranosyl)perimidine 8. The d-xylo-, d-galacto-, d-manno- and d-glycero analogues 12, 15, 16 and 19 were prepared similarly. The glycals 9 and 13 were formed as by-products resulting from elimination of acetic acid from the corresponding pyranosylperimidines. The structure of d-glucose-derived perimidine 8 was established by X-ray crystallography. 2010 Elsevier Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 21078510 DOI: 10.1016/j.carres.2010.09.028
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104