作者:Manfred Schlosser、Dominique Michel、Simon L. Croft
DOI:10.1055/s-1996-4262
日期:1996.5
In a successful attempt to amplify the pharmacological activity of the antimalarial bialamicol, substituents have been introduced in the 2-position of the allyl side chains. 2-Fluoroallyl bromide, a versatile C3F building block, is described for the first time.
为了提高抗疟药比亚拉米醇的药理活性,人们成功地在烯丙基侧链的 2 位引入了取代基。2-Fluoroallyl bromide(2-氟烯丙基溴)是一种多用途的 C3F 构建模块,它是首次被描述。