[1]Patent:CN109456153,2019,A.Locationinpatent:Paragraph0048-0062;0064
[2]HelveticaChimicaActa,1956,vol.39,p.2041,2046 JustusLiebigsAnnalenderChemie,1957,vol.603,p.129,137
[3]Tetrahedron,Supplement,1966,vol.8,p.1-7
[4]AgriculturalandBiologicalChemistry,1981,vol.45,p.791-794
[5]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.80-84
[1]Synthesis,2013,vol.45,p.615-620
[2]ChemicalCommunications,2015,vol.51,p.5852-5855
[3]Patent:CN105601490,2016,A.Locationinpatent:Paragraph0017;0018
[4]OrganicLetters,2006,vol.8,p.3149-3151
[5]ChemistryLetters,1984,p.2031-2032
[6]ChemischeBerichte,1987,vol.120,p.1133-1150
[7]EuropeanJournalofOrganicChemistry,2015,vol.2015,p.6472-6478
[8]TetrahedronLetters,1988,vol.29,p.765-768
[9]ChemistryLetters,1983,p.1081-1082
[10]ChemistryLetters,1983,p.1081-1082
[11]Chemistry-AEuropeanJournal,2005,vol.11,p.3899-3914
[12]AdvancedSynthesisandCatalysis,2011,vol.353,p.1447-1451
[13]BulletinoftheKoreanChemicalSociety,2012,vol.33,p.459-463
[14]RSCAdvances,2016,vol.6,p.90887-90896
[15]Patent:CN105481671,2016,A.Locationinpatent:Paragraph0008;0009
[16]ChemCatChem,2017,vol.9,p.3821-3826
[17]Patent:CN108911954,2018,A.Locationinpatent:Paragraph0037;0038;0045;0046;0053;0054;0061;0062
[18]Catalysisscienceandtechnology,2019,vol.9,p.1398-1405
[1]TetrahedronAsymmetry,1992,vol.3,p.443-450
[2]OrganicandBiomolecularChemistry,2006,vol.4,p.4186-4192
[1]Strauss,ChristopherR.;Wilson,Bevan;Williams,PatrickJ.[Phytochemistry,1987,vol.26,#7,p.1995-1998]
[1]HelveticaChimicaActa,1989,vol.72,p.365-369
[2]Patent:WO2010/147653,2010,A1.Locationinpatent:Page/Pagecolumn157
Title: Enoate reductases from non conventional yeasts: bioconversion, cloning, and functional expression in Saccharomyces cerevisiae.
Journal: Journal of biotechnology 20111220
Title: Bioreduction of α,β-unsaturated ketones and aldehydes by non-conventional yeast (NCY) whole-cells.
Journal: Bioresource technology 20110301
Title: Asymmetric reduction of activated alkenes using an enoate reductase from Gluconobacter oxydans.
Journal: Applied microbiology and biotechnology 20110101
Title: Volatile compounds in honey: a review on their involvement in aroma, botanical origin determination and potential biomedical activities.
Journal: International journal of molecular sciences 20110101
Title: Composition of sulla (Hedysarum coronarium L.) honey solvent extractives determined by GC/MS: norisoprenoids and other volatile organic compounds.
Journal: Molecules (Basel, Switzerland) 20100909
Title: Volatile composition screening of Salix spp. nectar honey: benzenecarboxylic acids, norisoprenoids, terpenes, and others.
Journal: Chemistry & biodiversity 20100901
Title: Quality and functionality of saffron: quality control, species assortment and affinity of extract and isolated saffron compounds to NMDA and sigma1 (sigma-1) receptors.
Journal: Planta medica 20080601
Title: Ketoisophorone transformation by Marchantia polymorpha and Nicotiana tabacum cultured cells.
Journal: Zeitschrift fur Naturforschung. C, Journal of biosciences 20080101
Title: A variety of volatile compounds as markers in unifloral honey from dalmatian sage (Salvia officinalis L.).
Journal: Chemistry & biodiversity 20061201
Title: Generation of aroma compounds from Ditaxis heterantha by Saccharomyces cerevisiae.
Journal: Applied microbiology and biotechnology 20060801
Title: In situ product recovery (ISPR) by crystallization: basic principles, design, and potential applications in whole-cell biocatalysis.
Journal: Applied microbiology and biotechnology 20060601
Title: Use of SPME-GC-MS in the study of time evolution of the constituents of saffron aroma: modifications of the composition during storage.
Journal: Journal of chromatographic science 20060101
Title: Cloning and overexpression of the old yellow enzyme gene of Candida macedoniensis, and its application to the production of a chiral compound.
Journal: Journal of biotechnology 20041019
Title: Anthropogenic organic contaminants in sediments of the Lippe river, Germany.
Journal: Water research 20040901
Title: In situ product removal using a crystallization loop in asymmetric reduction of 4-oxoisophorone by Saccharomyces cerevisiae.
Journal: Biotechnology and bioengineering 20040630
Title: Molecular markers of anthropogenic activity in sediments of the Havel and Spree Rivers (Germany).
Journal: Water research 20030601
Title: Old Yellow Enzyme from Candida macedoniensis catalyzes the stereospecific reduction of the C=C bond of ketoisophorone.
Journal: Bioscience, biotechnology, and biochemistry 20021201
Title: Chemicals with sweet aroma descriptors found in Portuguese wines from the Douro region: 2,6,6-trimethylcyclohex-2-ene-1,4-dione and diacetyl.
Journal: Journal of agricultural and food chemistry 20010101
Title: Hegazy ME, et al. Ketoisophorone transformation by Marchantia polymorpha and Nicotiana tabacum cultured cells. Z Naturforsch C. 2008 May-Jun;63(5-6):403-8.