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Synthesis of α-tocopherol and naphthotocopherol analogs with a carboxyl group in the side chain

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Abstract

On the basis of ozonolysis of short-chain α-tocopherol and naphthotocopherol analogs with a terminal isopropylidene group in the side chain, a general approach to the synthesis of 6-hydroxy-2,5,7,8-tetrtamethylchroman-2-yl-and 6-hydroxy-2,5-dimethyl-3,4-dihydro-2H-naphtho[1,2-b]pyran-2-ylpropionic and-acetic acid derivatives, which are hydrophilic tocopherol analogs, was proposed.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 2, pp. 299—304, February, 2006.

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Spivak, A.Y., Knyshenko, O.V., Mallyabaeva, M.I. et al. Synthesis of α-tocopherol and naphthotocopherol analogs with a carboxyl group in the side chain. Russ Chem Bull 55, 306–311 (2006). https://doi.org/10.1007/s11172-006-0253-8

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  • DOI: https://doi.org/10.1007/s11172-006-0253-8

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