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Synthesis and structure of 1,2-O-isopropylidene-α-D-glucofuranose 3,5-phenylcyclophosphonate

✍ Scribed by N. S. Magomedova; A. N. Sobolev; M. P. Koroteev; N. M. Pugashova; V. K. Bel'skii; É. E. Nifant'ev


Publisher
SP MAIK Nauka/Interperiodica
Year
1992
Tongue
English
Weight
418 KB
Volume
32
Category
Article
ISSN
0022-4766

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Specific synthesis and stereochemical as
✍ Karin Åkerfeldt; Paul A. Bartlett 📂 Article 📅 1986 🏛 Elsevier Science 🌐 English ⚖ 515 KB

Pyridinium tosylate-catalyzed a&al exchange between benxaldehyde dimethyl acetal and 6-O-(tert-butyldiphenylsilyl)-l,2-O-isopropylidene-a-D-glucofuranose was investigated as an alternative to the original procedure of Brigl and Grtiner (condensation of a D-glucose trio1 with benxaldehyde under zinc