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Improvement on the Synthesis of Primary Amino Sugar Derivatives <i>via</i><i>N</i>-Benzyl Intermediates
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作者 massimo corsi Marco Bonanni +3 位作者 Giorgio Catelani Felicia D’Andrea Tiziana Gragnani Roberto Bianchini 《International Journal of Organic Chemistry》 2013年第3期41-48,共8页
Primary tosylates 1a-d were converted to the corresponding amino species 3a-d. Benzylamine was proved effective for the substitution of tosylates, using acetonitrile (MeCN) as the solvent of choice and citric acid to ... Primary tosylates 1a-d were converted to the corresponding amino species 3a-d. Benzylamine was proved effective for the substitution of tosylates, using acetonitrile (MeCN) as the solvent of choice and citric acid to remove excess of the reagent from crude products 2a-d. Debenzylation was carried out at circa (ca.) atmospheric pressure of hydrogen gas in the presence of acetic acid (AcOH). The method was also demonstrated in a demo batch experiment for the synthesis of compound 3a on a 50 g scale of 1a. 展开更多
关键词 Amino Sugars NUCLEOPHILIC Substitution BENZYLAMINE PRIMARY TOSYLATES
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