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Total synthesis of (+)-obtusenyne
Authors:Toshiyuki Uemura  Naohiro Onodera  Takashi Hoshi
Institution:a Graduate School of Science and Technology, Niigata University, 2-nocho, Ikarashi, Niigata 950-2181, Japan
b Faculty of Engineering, Niigata University, 2-nocho, Ikarashi, Niigata 950-2181, Japan
Abstract:The stereoselective total synthesis of (+)-obtusenyne is described. The oxonene skeleton possessing trans-orientated alkyl substituents at the α,α′-positions was stereoselectively constructed via cyclization of the corresponding hydroxy epoxide promoted by Eu(fod)3.
Keywords:(+)-Obtusenyne  Oxonenes  Medium-ring heterocycles  Cyclization  Hydroxy epoxides
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