Abstract
Resolution of racemic 2-isobornyl-4-methylphenol into enantiomers was performed following its transformation into diastereomers by the reaction with (1S)-camphanoyl chloride.
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Dedicated to Academician of the Russian Academy of Sciences I. L. Eremenko on the occasion of his 60th birthday.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1271–1272, June, 2010.
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Buravlev, E.V., Chukicheva, I.Y. & Kutchin, A.V. Resolution of racemic 2-isobornyl-4-methylphenol into enantiomers. Russ Chem Bull 59, 1300–1301 (2010). https://doi.org/10.1007/s11172-010-0237-6
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DOI: https://doi.org/10.1007/s11172-010-0237-6