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3-quinuclidinone and quinuclidines

3-quinuclidinone has been researched along with quinuclidines in 8 studies

*Quinuclidines: A class of organic compounds which contain two rings that share a pair of bridgehead carbon atoms and contains an amine group. [MeSH]

*Quinuclidines: A class of organic compounds which contain two rings that share a pair of bridgehead carbon atoms and contains an amine group. [MeSH]

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (12.50)18.2507
2000's4 (50.00)29.6817
2010's3 (37.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Anderson, VE; Bahnson, BJ; D'Ordine, RL; Tonge, PJ1
Barták, P; Bednár, P; Hlavác, J; Lemr, K; Sevcík, J; Stránský, Z; Stýskala, J; Wiedermannová, I1
Crooks, PA; Freeman, ML; Sasi, S; Sekhar, KR; Sonar, VN; Thirupathi Reddy, Y1
Kataoka, M; Nishimoto, Y; Nomoto, F; Sakoda, A; Shimizu, S; Uzura, A1
Kataoka, M; Miyakawa, T; Miyazono, K; Nagata, K; Shimizu, S; Takeshita, D; Tanokura, M; Uzura, A1
Isotani, K; Itoh, N; Kurokawa, J; Matsuda, M; Negishi, T; Nomoto, S; Suzuki, F1
Huang, L; Pan, J; Xu, GC; Xu, JH; Yu, HL; Zhang, WX1
Hou, F; Kataoka, M; Kumashiro, S; Miyakawa, T; Nagata, K; Shimizu, S; Takeshita, D; Tanokura, M; Urano, N; Uzura, A1

Other Studies

8 other study(ies) available for 3-quinuclidinone and quinuclidines

ArticleYear
Enoyl-coenzyme A hydratase-catalyzed exchange of the alpha-protons of coenzyme A thiol esters: a model for an enolized intermediate in the enzyme-catalyzed elimination?
    Biochemistry, 1994, Dec-13, Volume: 33, Issue:49

    Topics: Acyl Coenzyme A; Animals; Catalysis; Cattle; Enoyl-CoA Hydratase; Esters; Liver; Magnetic Resonance Spectroscopy; Models, Chemical; Protons; Quinuclidines; Rats; Stereoisomerism; Sulfhydryl Compounds

1994
Capillary electrophoresis/mass spectrometry: a promising tool for the control of some physiologically hazardous compounds. I-derivatives of 3-quinuclidinol.
    Journal of mass spectrometry : JMS, 2002, Volume: 37, Issue:12

    Topics: Electrophoresis, Capillary; Fresh Water; Hallucinogens; Mass Spectrometry; Molecular Structure; Quinuclidines; Quinuclidinyl Benzilate; Sensitivity and Specificity; Water Pollutants

2002
Novel substituted (Z)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-one and (Z)-(+/-)-2-(N-benzylindol-3-ylmethylene)quinuclidin-3-ol derivatives as potent thermal sensitizing agents.
    Bioorganic & medicinal chemistry letters, 2007, Dec-15, Volume: 17, Issue:24

    Topics: Cell Line, Tumor; Cell Survival; Humans; Molecular Structure; Quinuclidines; Radiation-Sensitizing Agents; Structure-Activity Relationship; Temperature

2007
Stereoselective synthesis of (R)-3-quinuclidinol through asymmetric reduction of 3-quinuclidinone with 3-quinuclidinone reductase of Rhodotorula rubra.
    Applied microbiology and biotechnology, 2009, Volume: 83, Issue:4

    Topics: Alcohol Oxidoreductases; Amino Acid Sequence; Base Sequence; Biotransformation; Cloning, Molecular; DNA, Fungal; Escherichia coli; Fungal Proteins; Gene Expression; Glucose 1-Dehydrogenase; Molecular Sequence Data; Quinuclidines; Rhodotorula; Sequence Analysis, DNA; Sequence Homology, Amino Acid; Stereoisomerism

2009
Crystallization and preliminary X-ray analysis of the NADPH-dependent 3-quinuclidinone reductase from Rhodotorula rubra.
    Acta crystallographica. Section F, Structural biology and crystallization communications, 2009, Jun-01, Volume: 65, Issue:Pt 6

    Topics: Alcohol Oxidoreductases; Aldehyde Reductase; Aldo-Keto Reductases; Catalysis; Cloning, Molecular; Crystallization; Crystallography, X-Ray; Data Collection; Escherichia coli; Genetic Vectors; Hydrogen-Ion Concentration; Plasmids; Quinuclidines; Rhodotorula; Statistics as Topic; Substrate Specificity; Temperature; Transformation, Bacterial; X-Ray Diffraction

2009
Gene cloning and characterization of two NADH-dependent 3-quinuclidinone reductases from Microbacterium luteolum JCM 9174.
    Applied and environmental microbiology, 2013, Volume: 79, Issue:4

    Topics: Actinomycetales; Amino Acid Sequence; Cloning, Molecular; Coenzymes; DNA, Bacterial; Escherichia coli; Molecular Sequence Data; NAD; Oxidoreductases; Quinuclidines; Recombinant Fusion Proteins; Sequence Alignment; Sequence Analysis, DNA; Substrate Specificity

2013
Highly efficient synthesis of (R)-3-quinuclidinol in a space-time yield of 916 g L(-1) d(-1) using a new bacterial reductase ArQR.
    Organic letters, 2013, Oct-04, Volume: 15, Issue:19

    Topics: 3-Hydroxyacyl-CoA Dehydrogenase; Escherichia coli; Quinuclidines; Stereoisomerism

2013
Structural basis for high substrate-binding affinity and enantioselectivity of 3-quinuclidinone reductase AtQR.
    Biochemical and biophysical research communications, 2014, Apr-18, Volume: 446, Issue:4

    Topics: Agrobacterium tumefaciens; Binding Sites; Crystallography, X-Ray; Models, Molecular; NAD; Oxidoreductases; Protein Conformation; Quinuclidines; Stereoisomerism; Substrate Specificity

2014