中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Oxidation of the norditerpenoid alkaloids isotalatizidine and 6-epiforsticine

文献类型:期刊论文

作者Li, ZB ; Chen, QH ; Wang, FP ; Li, BG
刊名CHINESE CHEMICAL LETTERS
出版日期2000
卷号11期号:5页码:421_424
关键词norditerpenoid alkaloid oxidation isotalatizidine 6-epiforsticine Curvularia lunata
ISSN号1001-8417
产权排序2
中文摘要Oxidation of 1 with KMnO4 in acetone-H2O (1:1) for 1h gave nevadenine 2 (38%). But. 3 was Formed in 98% yield when prolonging time and raising temperature (40 degrees C). Reaction of 1 and 10 with Conforth reagent afforded the ketones 11 (55%), 12 (30%), and 13 (13%), 14 (20%), respectively. While oxidation of 7 and 15 with a variety of the oxidizing agents gave 17 only in low 20% of yield besides the minor 16. In addition, 1 was converted to 2 by the fungi Curvularia lunata.
学科主题Chemistry, Multidisciplinary
收录类别SCI
语种英语
WOS记录号WOS:000087193800018
公开日期2011-07-08
源URL[http://210.75.237.14/handle/351003/17131]  
专题成都生物研究所_天然产物研究
推荐引用方式
GB/T 7714
Li, ZB,Chen, QH,Wang, FP,et al. Oxidation of the norditerpenoid alkaloids isotalatizidine and 6-epiforsticine[J]. CHINESE CHEMICAL LETTERS,2000,11(5):421_424.
APA Li, ZB,Chen, QH,Wang, FP,&Li, BG.(2000).Oxidation of the norditerpenoid alkaloids isotalatizidine and 6-epiforsticine.CHINESE CHEMICAL LETTERS,11(5),421_424.
MLA Li, ZB,et al."Oxidation of the norditerpenoid alkaloids isotalatizidine and 6-epiforsticine".CHINESE CHEMICAL LETTERS 11.5(2000):421_424.

入库方式: OAI收割

来源:成都生物研究所

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