Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 130, Issue 29, Pages 9214-+Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja803094u
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- NIGMS NIH HHS [R01 GM073855-02, R01 GM073855, GM-073855] Funding Source: Medline
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An efficient approach to cyclohexenyl chalcones employing highly electron rich 2'-hydroxychalcone dienophiles via electron transfer-initiated Diels-Alder cycloaddition is described. Using the methodology, the total synthesis of nicolaiodesin C has been accomplished.
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