化学
区域选择性
亲核细胞
催化作用
药物化学
有机化学
作者
Leticia Lafuente,María Florencia Rochetti,Rodolfo D. Bravo,Leandro D. Sasiambarrena,Cintia C. Santiago,Agustı́n Ponzinibbio
出处
期刊:Letters in Organic Chemistry
[Bentham Science]
日期:2018-10-22
卷期号:16 (6): 447-453
被引量:11
标识
DOI:10.2174/1570178615666181022145338
摘要
Cu-Fe spinels promoted the Ferrier rearrangement of 2-nitroglycals with several O-nucleophiles. 2,3-Unsaturated carbohydrate derivatives were prepared by the reaction of 3,4,6-tri-Oacetyl- 2-nitroglucal and alcohols in the presence of 5 % of CuFe2O4. After separation of the catalyst with an external magnet, the reaction products were obtained in good yields and high stereo and regioselectivity. Also, S- and heterocyclic C-3 substituted 2-nitro-endo-glycals could be prepared by this method.
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