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Antitumor Agents 274. A New Synthetic Strategy for E-ring SAR Study of Antofine and Cryptopleurine Analogs

[Image: see text] A new versatile synthetic methodology for the synthesis of enantiomerically pure natural phenanthroindolizidines and phenanthroquinolizidines has been established and described. Natural products R-antofine and R-cryptopleurine, as well as a novel E-ring expanded analog 13c (E7), 12...

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Библиографические подробности
Главные авторы: Yang, Xiaoming, Shi, Qian, Bastow, Kenneth F., Lee, Kuo-Hsiung
Формат: Artigo
Язык:Inglês
Опубликовано: 2010
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2849728/
https://ncbi.nlm.nih.gov/pubmed/20196574
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/ol902819j
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