Chang Chi-Fen, Li Chien-Fu, Tsai Chia-Chen, Chuang Ta-Hsien
Department of Anatomy, School of Medicine, China Medical University , Taichung 40402, Taiwan.
School of Pharmacy, China Medical University , Taichung 40402, Taiwan.
Org Lett. 2016 Feb 19;18(4):638-41. doi: 10.1021/acs.orglett.5b03395. Epub 2016 Feb 2.
Phenanthroindolizidines and phenanthroquinolizidines were concisely synthesized by the reductive decyanization of cyano-promoted intramolecular aza-Diels-Alder cycloadducts followed by aryl-aryl coupling. Cyano groups were removed from α-aminoacrylonitriles via treatment with sodium borohydride in 2-propanol in almost quantitative yields; a possible mechanism was proposed and examined using D-labeling experiments. A systematic study of the effects of the phenanthrene substitution pattern on the anticancer activity against three human cancer cell lines was discussed.
通过氰基促进的分子内氮杂-狄尔斯-阿尔德环加成物的还原脱氰,随后进行芳基-芳基偶联,简洁地合成了菲并吲哚里西定和菲并喹诺里西定。通过在2-丙醇中用硼氢化钠处理,几乎以定量产率从α-氨基丙烯腈中除去氰基;提出了一种可能的机理,并通过氘标记实验进行了研究。讨论了菲取代模式对三种人类癌细胞系抗癌活性影响的系统研究。