Alternative Mild Route to the Synthesis of 4-Methylenecyclohex-2-enone, a Key Moiety of the Anticancer Compounds Ottelione A and B
Author:
Affiliation:
1. a University College Dublin , Dublin , Ireland
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2011.607936
Reference12 articles.
1. Otteliones A and B: Potently Cytotoxic 4-Methylene-2-cyclohexenones from Ottelia alismoides
2. A revision of the genus Ottelia (hydrocharicaea) I. Generic considerations
3. Enantioselective total syntheses of (+)- and (−)-ottelione A and (+)- and (−)-ottelione B. Absolute configuration of the novel, biologically active natural products
4. Natural, semisynthetic and synthetic microtubule inhibitors for cancer therapy
Cited by 4 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. Unconventional exo selectivity in thermal normal-electron-demand Diels–Alder reactions;Scientific Reports;2016-10-12
2. The synthesis and biological testing of bacilysin analogues;Amino Acids;2013-08-06
3. Enantioselective Total Synthesis of Otteliones A and B, Novel and Powerful Antitumor Agents from the Freshwater Plant Ottelia alismoides;Natural Product Communications;2013-07
4. ChemInform Abstract: Alternative Mild Route to the Synthesis of 4-Methylenecyclohex-2-enone, a Key Moiety of the Anticancer Compounds Ottelione A and B.;ChemInform;2012-08-23
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