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High Stereoselective Glycosylation of Calix[4]arenes with α-Acetobromoglucopyranoside
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作者 Zhan Jiang LI and Zhi Tang HUANG(Institute of Chedristry, Acgademia Sinica, Bejing 100080) 《Chinese Chemical Letters》 SCIE CAS CSCD 1997年第5期369-372,共4页
Glycosylation of calix[4]arenes with a - acetobromoglucopyanoside 1 inacetonitrile in the presence of potassium carbonate or calcium hydride under mildconditions gave sugar calix[4]arenes 4 and 5 in good yields, and ... Glycosylation of calix[4]arenes with a - acetobromoglucopyanoside 1 inacetonitrile in the presence of potassium carbonate or calcium hydride under mildconditions gave sugar calix[4]arenes 4 and 5 in good yields, and β-anomers were thesole products with high stereoselectivity. Compound 4 or 5 were dealt with anunoniain methyl alcohol to afford the Waer-soluble calix[4]arenes derivatives 6 and 7. 展开更多
关键词 High Stereoselective Glycosylation of arenes with acetobromoglucopyranoside
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