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Synthesis of 2,2-Dialkyl Chromanes by Intramolecular Ullmann C-O Coupling Reactions toward the Total Synthesis of D-α-Tocopherol.

作者信息

Tsubogo Tetsu, Aoyama Saki, Takeda Rika, Uchiro Hiromi

机构信息

Faculty of Pharmaceutical Sciences, Tokyo University of Science.

Division of Fusion of Regenerative Medicine with DDS, Research Institute for Science and Technology (RIST), Tokyo University of Science.

出版信息

Chem Pharm Bull (Tokyo). 2018;66(9):843-846. doi: 10.1248/cpb.c18-00460.

Abstract

The complete synthesis of D-α-tocopherol was achieved using our developed-Ullmann C-O coupling reaction as a key reaction. The synthesis of the core structure of D-α-tocopherol, which is a chiral chromane, has never been reported using intramolecular Ullmann C-O coupling reactions owing to the low reactivity of electron-rich iodoarenes with tertiary alcohols. Because the developed intramolecular C-O coupling reactions prefer electron-rich iodoarenes with tertiary alcohols, we successfully synthesized the chiral chromane core and achieved the total synthesis of D-α-tocopherol.

摘要

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