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Chem Pharm Bull (Tokyo) ; 66(9): 843-846, 2018.
Article in English | MEDLINE | ID: mdl-30175739

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.


Subject(s)
Chromans/chemical synthesis , alpha-Tocopherol/chemical synthesis , Alcohols/chemistry , Amides/chemistry , Catalysis , Cyclization , Isomerism , Molecular Structure , Oxidation-Reduction
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