Abstract
The progenitors of damascenone (1), the most intensive C13-norisoprenoid volatile aroma constituent of rose essential oil, were surveyed in the flowers of Rosa damascena Mill. Besides 9-O-β-D-glucopyranosyl-3-hydroxy-7,8-didehydro-β-ionol (4b), a stable progenitor already isolated from the residual water after steam distillation of flowers of R. damascena Mill., two labile progenitors were identified to be (3S, 9R)- and (3S, 9S)-megastigma-6,7-dien-3,5,9-triol 9-O-β-D-glucopyranosides (2b) based on their synthesis and HPLC-MS analytical data. Compound 2b gave damascenone (1), 3-hydroxy-β-damascone (3) and 4b upon heating under acidic conditions. © 2002 by Japan Society for Bioscience, Biotechnology, and Agrochemistry.
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Suzuki, M., Matsumoto, S., Mizoguchi, M., Hirata, S., Takagi, K., Hashimoto, I., … Watanabe, N. (2002). Identification of (3S, 9R)- and (3S, 9S)-Megastigma-6,7-dien-3,5,9-triol 9-O-b-D-glucopyranosides as Damascenone Progenitors in the Flowers of Rosa damascena Mill. Bioscience, Biotechnology and Biochemistry, 66(12), 2692–2697. https://doi.org/10.1271/bbb.66.2692
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