Journal
ORGANIC LETTERS
Volume 14, Issue 18, Pages 4878-4881Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol302205w
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Funding
- National Science of Foundation of China [21102081, 21133002]
- China's 985 project [411307141]
- New Teachers' Fund for Doctor Stations, Ministry of Education [20110002120011]
- Shenzhen Peacock program
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A concise biomimetic total synthesis of incarvilleatone and incarviditone is achieved in one pot via the highly stereoselective hetero- and homodimerization of (+/-)-rengyolone, respectively. The structure of incarviditone is revised on the basis of spectroscopic and computational evidence.
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