Novel Product and Its Derivatives from the Reaction of Lappaconitine with HIO_4
Novel Product and Its Derivatives from the Reaction of Lappaconitine with HIO_4
摘要
Treatment of lappaconitine 1 with HIO4 at room temperature afforded 2 in 41% yield, to which Br2-HOAc solution was added and allowed to stand at room temperature for 2 days to give 3 (13%) and 4(31%).
Treatment of lappaconitine 1 with HIO4 at room temperature afforded 2 in 41% yield, to which Br2-HOAc solution was added and allowed to stand at room temperature for 2 days to give 3 (13%) and 4(31%).
参考文献2
-
1F. N. Dzhakhangirov,M. N. Sultankhodzhaev,B. Tashkhodzhaev,B. T. Salimov.Diterpenoid alkaloids as a new class of antiarrhythmic agents. Structure-activity relationship[J].Chemistry of Natural Compounds.1997(2)
-
2S. W. Pelletter,N. V. Mody,R. S. Sawhney,Can. Journal of Chemistry . 1979
-
1Qiao Hong CHEN,Feng Peng WANG.NaIO_4-Catalyzed Bromination of the Aromatic Ring of Lappaconitine[J].Chinese Chemical Letters,2001,12(5):421-424.
-
2Kai Jun LIAO,Xiao Hua YAN,Dong Yun ZHAO,Xue Yi MA.DSC and NMR Study on the Inclusion Complex of Lappaconitine with b-Cyclodextrin[J].Chinese Chemical Letters,2002,13(3):227-230.
-
3辛蕊华,程富胜,胡振英,倪京满.高乌甲素的研究概况[J].中兽医医药杂志,2009,28(2):74-76. 被引量：12
-
4Liao Kaijun.Study on the Supramolecular Inclusion Complex of[J].Chemical Research in Chinese Universities,2001,17(z1):166-167.
