Preparation of α-damascone
Author:
Affiliation:
1. University of Science and Technology Liaoning , School of Chemical Engineering , Liaoning Anshan , 114051 , P. R. China
2. Jijia Geen Bilding Tchnology co., LTD, Liaoning Anshan , 114051 , P. R. China
Abstract
Publisher
Walter de Gruyter GmbH
Subject
General Chemical Engineering,General Chemistry,Biotechnology
Link
https://www.sciendo.com/pdf/10.2478/pjct-2019-0009
Reference10 articles.
1. 1. Anthony, J.N.B., Stephen, W.P. & John, S.S. (1983) A damascone derivative from Nicotiana tabacum. Phytochemistry. 22(2), 613–614. DOI: 10.1016/0031-9422(83)83068-4.10.1016/0031-9422(83)83068-4
2. 2. Kenji, M. & Masayasu, A. (1993) Synthesis of (S)-α-damascone. Tetrahedron. 49(9), 1871–1878. DOI: 10.1016/S0040-4020(01)80543-3.10.1016/S0040-4020(01)80543-3
3. 3. Werkhoff, P., Bretschneider, W. & Güntert, M., et al. (1991) Chirospecific analysis in flavor and essential oil chemistry Part B. Direct enantiomer resolution of frans-α-ionone and trans-α-damascone by inclusion gas chromatography. Z. Lebensm.--Unters. Forsch. 192(2), 111–115. DOI: 10.1007/BF01202622.10.1007/BF01202622
4. 4. Ohloff, G. & Uhde, G. (2004) Über eine ungewöhnliche Cyclisationsreaktion bei der Umsetzung von (+)-Epoxy-α-dihydrojonon mit Hydrazinhydrat. Helv. Chim. Acta. 53(3): 531–541. DOI: 10.1002/hlca.19700530309.10.1002/hlca.19700530309
5. 5. Stefano, S. & Claudio, F. (2006) Synthesis of the enantiomeric forms of α- and γ-damascone starting from commercial racemic α-ionone. Tetrahedron Asymmetry. 17(10), 1573–1580. DOI: 10.1016/j.tetasy.2006.05.024.10.1016/j.tetasy.2006.05.024
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