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

Tetsu Tsubogo, Saki Aoyama, Rika Takeda, Hiromi Uchiro

Chemical and Pharmaceutical Bulletin · 2018 · 10 citations · 39 references

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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.

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