Author:
Kazakova O. B.,Yamansarov E. Yu.,Kukovinets O. S.,Medvedeva N. I.,Kazakov D. V.,Kornilov O. K.,Suponitskii K. Yu.
Publisher
Springer Science and Business Media LLC
Subject
Plant Science,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Reference10 articles.
1. K. Griesbaum, Trends Org. Chem., 6, 145 (1997).
2. K. Griesbaum, X. Liu, A. Kassiaris, and M. Scherer, Liebigs Ann., 1381 (1997).
3. G.-J. Ten Brink, I. W. C. E. Arends, and R. A. Sheldon, Chem. Rev., 104, 4105 (2004).
4. R. T. Aplin, R. P. K. Chan, and T. G. Halsall, J. Chem. Soc. C, 2322 (1969).
5. P. S. Bailey, Chem. Rev., 58, 925 (1958).
Cited by
10 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Oxidation of 3β-Acetoxy-21β-acetyl-20β,28-epoxy-18α,19βH-ursane into Novel gem-Chloronitro- and 1,2,4,5-tetraoxane derivatives;Natural Product Communications;2018-03
2. Synthesis and antimalarial activity of 3′-trifluoromethylated 1,2,4-trioxolanes and 1,2,4,5-tetraoxane based on deoxycholic acid;Steroids;2018-01
3. Synthesis of triterpenoid-based ring-A azepanone and gem-3-nitro-3-chloro- derivatives by ozonolysis of 3-oximino-28-oxoallobetulin under normal and acidic solvolysis conditions;Tetrahedron;2017-07
4. Inhibition of Alpha-Glucosidase by Synthetic Derivatives of Lupane, Oleanane, Ursane and Dammarane Triterpenoids;Natural Product Communications;2016-01
5. Molecular structure of 3-OXO-URS-12-EN-28-OIC acid anhydride;Journal of Structural Chemistry;2015-09