منابع مشابه
Photo-Oxygenation of Trans Anethole
Photo-oxygenation of trans anethole (1), the main constituent of anise essential oil, using tetraphenylporphyrine (TPP) as a singlet oxygen sensitizer in chloroform gave 4-methoxybenzaldehyde (p-anisaldhyde) (2), 2-(4-methoxyphenyl)propan-2-ol (3) as well as erythro and threo 1-(4-methoxyphenyl)propane-1,2-diol (4a, 4b). The structures of the photo-oxygenation products were elucidated by spectr...
متن کاملA New Sulfated α-Ionone Glycoside from Sonchus erzincanicus Matthews
Sonchus erzincanicus (Asteraceae) is an endemic species in Turkey, where six Sonchus species grow. In this study, a phytochemical study was performed on the aerial parts of the plant. The study describes the isolation and structure elucidation of five flavonoids and two α-ionone glycosides from S. erzincanicus. The compounds were isolated using several and repeated chromatographic techniques fr...
متن کاملBiosynthesis of α- and β-ionone, prominent scent compounds, in flowers of Osmanthus fragrans.
Carotenoid derived volatiles are important fragrance compounds, which contribute to the scents of flowers from diverse taxa. A famous example is represented by the flowers of Osmanthus fragrans where apocarotenoids account for more than 20% of all volatiles. In the recent years, bio-degradation of carotenoids has been shown to be an important route for apocarotenoids formation. Here, we report ...
متن کاملHighly selective and asymmetric reductive biotransformation of α-ionone by Epicoccum purpurascens.
The biotransformation of terpenoid C13 norisoprenoid (±)-α-ionone (1) using the plant pathogenic fungus Epicoccum purpurascens as a biocatalyst was investigated for the production of useful novel organic compounds. There are no reported biotransformations using E. purpurascens. The biotransformation of compound 1 via reduction of the C-9 ketone position yielded α-ionol (2) as the major metaboli...
متن کاملA Practical Chemo-enzymatic Approach to Highly Enantio-Enriched 10-Ethyl-7,8-dihydro-γ-ionone Isomers: A Method for the Synthesis of 4,5-Didehydro-α-Ionone
An efficient and convenient strategy for the enantioselective synthesis of enantiomerically enriched 10-ethyl-7,8-dihydro-γ-ionone isomers (R)-(+)-7, and (S)-(-)-7 are described utilizing a lipase mediated resolution protocol, and reductive elimination of the secondary allylic alcohol as the key step. The enantioselective and diastereoselective lipase kinetic acetylation of 4-hydroxy-γ-ionone d...
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ژورنال
عنوان ژورنال: Agricultural and Biological Chemistry
سال: 1972
ISSN: 0002-1369,1881-1280
DOI: 10.1271/bbb1961.36.1091