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Access to enantiomerically pure intermediates for (−)-geosmin synthesis starting from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methyl-naphthalen-2(3H)-one

Bioscience, Biotechnology and Biochemistry (2002) 66(10) 2267-2272
DOI: 10.1271/bbb.66.2267
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Abstract

Enantiomerically pure key intermediates for the synthesis of the natural enantiomer of geosmin were synthesized from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methylnaphthalen-2(3H)-one. © 1999 by Japan Society for Bioscience, Biotechnology, and Agrochemistry.

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Fuhshuku, K. I., & Sugai, T. (2002). Access to enantiomerically pure intermediates for (−)-geosmin synthesis starting from (4aS,5S)-4,4a,5,6,7,8-hexahydro-5-hydroxy-4a-methyl-naphthalen-2(3H)-one. Bioscience, Biotechnology and Biochemistry, 66(10), 2267–2272. https://doi.org/10.1271/bbb.66.2267

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