Total chemical synthesis and antitumor evaluation of 4-demethoxy-10,10-dimethyldaunomycin
摘要:
The novel anthracycline analogue 4-demethoxy-10,10-dimethyldaunomycin was prepared in nine chemical steps from 5,8-dimethoxy-2-tetralone. It proved to be inactive as an antitumor agent in the mouse P388 lymphocytic leukemia model.
Total chemical synthesis and antitumor evaluation of 4-demethoxy-10,10-dimethyldaunomycin
作者:Jose Alexander、Ish Khanna、Daniel Lednicer、Lester A. Mitscher、Tarik Veysoglu、Zbigniew Wielogorski、Richard L. Wolgemuth
DOI:10.1021/jm00376a021
日期:1984.10
The novel anthracycline analogue 4-demethoxy-10,10-dimethyldaunomycin was prepared in nine chemical steps from 5,8-dimethoxy-2-tetralone. It proved to be inactive as an antitumor agent in the mouse P388 lymphocytic leukemia model.