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- Towards the synthesis of calotropin and related cardenolides from 3-epiandrosterone: A-ring related modifications. Vanessa Koch, Martin Nieger, Stefan Bräse
, Org. Chem. Front.
, 2020
, 7
, 2670
- Cardenolide glycosides with 5,6-unsaturation from Asclepias vestita. H. T. Andrew Cheung, Carolyn J. Nelson
, J. Chem. Soc., Perkin Trans. 1
, 1989
, 1563
- 405. Cardenolides. Part VI. Uscharidin, calotropin, and calotoxin. D. H. G. Crout, C. H. Hassall, T. L. Jones
, J. Chem. Soc.
, 1964
, 2187
- A review on phytochemical constituents and pharmacological potential of Calotropis procera. Barkha Darra Wadhwani, Deepak Mali, Pooja Vyas, Rashmy Nair, Poonam Khandelwal
, RSC Adv.
, 2021
, 11
, 35854
- New glucoside conjugates and other cardenolide glycosides from the monarch butterfly reared on Asclepias fruticosa L.. H. T. Andrew Cheung, Carolyn J. Nelson, Thomas R. Watson
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 1851
- Cardenolide glycosides of the asclepiadaceae. New glycosides from asclepias fruticosa and the stereochemistry of uscharin, voruscharin and calotoxin. H. T. Andrew Cheung, Francis C. K. Chiu, Thomas R. Watson, Robert J. Wells
, J. Chem. Soc., Perkin Trans. 1
, 1983
, 2827
- Stereochemistry of the hexosulose in cardenolide glycosides of the asclepiadaceae. H. T. Andrew Cheung, Thomas R. Watson
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 2162
- Structures, chemotaxonomic significance, cytotoxic and Na+,K+-ATPase inhibitory activities of new cardenolides from Asclepias curassavica. Rong-Rong Zhang, Hai-Yan Tian, Ya-Fang Tan, Tse-Yu Chung, Xiao-Hui Sun, Xue Xia, Wen-Cai Ye, David A. Middleton, Natalya Fedosova, Mikael Esmann, Jason T. C. Tzen, Ren-Wang Jiang
, Org. Biomol. Chem.
, 2014
, 12
, 8919
- Twenty-five years of chemical ecology. Jeffrey B. Harborne
, Nat. Prod. Rep.
, 2001
, 18
, 361
- Stereoselective semisynthesis of uzarigenin and allo-uzarigenin. Sarah Al Muthafer, Christoph Schissler, Vanessa Koch, Hannes Kühner, Martin Nieger, Stefan Bräse
, Org. Chem. Front.
, 2023
, 10
, 1435