乙酰苯胺
醋酸酐
化学
甲醇
碘海索
乙酰化
有机化学
药物化学
核化学
催化作用
生物化学
基因
肾功能
作者
Torfinn Håland,Leiv K. Sydnes
摘要
Acetylation of 1 with acetic anhydride, an important step in the preparation of iohexol, gave the corresponding acetanilide and minor amounts of a few byproducts, whose structures have been elucidated. Among the byproducts were some 1,3-oxazolidines which survived when the reaction was quenched by adding methanol and water under strong acidic conditions.
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