节点文献
Rodgersinine A和B的全合成(英文)
Total synthesis of rodgersinine A and B
【摘要】 目的合成苯并二氧六环类新木脂素。方法综合使用多种有机合成反应来合成 Rodgersinine A,4-(3-甲基-7-(E)-1-丙烯基-2,3-二氢-1,4-二氧六环)-1,2-苯二酚和Rodgersinine B,4-(3-甲基-7-(1-丙炔基)-2,3-二氢-1,4-二氧六环)-1,2-苯二酚。结果首次合成了目标分子 Rodgersinine A和B。结论本文建立的合成方法可用于苯并二氧六环类新木脂素的合成。
【Abstract】 Aim Syntheses of benzodioxane neolignans. Method The SN2 reaction and Corey-Fuchs reaction was used to synthesize Rodgersinine A, 4-[3-methyl-7-[(E)-1-propenyl-2, 3-dihydro-1, 4-benzodioxin-2-yl]-1, 2-benzenediol (1) and Rodgersinine B, 4- [3-methyl-7-(1-propynyl)-2, 3-dihydro-1, 4-benzodioxin-2-yl]-1, 2-benzenediol (2). Results Total synthesis of Rodgersinine A and B was first completed. Conclusion A useful method for constructing benzodioxane neolignans by the SN2 reaction is achieved.
【关键词】 Corey-Fuchs反应;
酸关环;
SN2亲核取代反应;
炔类官能团;
【Key words】 Corey-Fuchs reaction; Closed ring by acid; SN2 reaction; Acetylenic functionality;
【Key words】 Corey-Fuchs reaction; Closed ring by acid; SN2 reaction; Acetylenic functionality;
【基金】 Program for Changjiang Scholars and Innovative Team in University(985-2-063-112).
- 【文献出处】 Journal of Chinese Pharmaceutical Sciences ,中国药学(英文版) , 编辑部邮箱 ,2007年01期
- 【分类号】O621.3
- 【被引频次】2
- 【下载频次】150