phosphoric acid and 1,2,3,4-tetrahydroquinoline

phosphoric acid has been researched along with 1,2,3,4-tetrahydroquinoline in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's5 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dagousset, G; Masson, G; Zhu, J1
Bernardi, L; Caruana, L; Fochi, M; Mazzanti, A; Ranieri, S1
Huang, Y; Luo, C1
Cai, XF; Chen, MW; Chen, ZP; Shi, L; Zhou, YG1
Akiyama, T; Miyashita, H; Saito, K1

Other Studies

5 other study(ies) available for phosphoric acid and 1,2,3,4-tetrahydroquinoline

ArticleYear
Chiral phosphoric acid-catalyzed enantioselective three-component Povarov reaction using enecarbamates as dienophiles: highly diastereo- and enantioselective synthesis of substituted 4-aminotetrahydroquinolines.
    Journal of the American Chemical Society, 2011, Sep-21, Volume: 133, Issue:37

    Topics: Carbamates; Catalysis; Phosphoric Acids; Quinolines; Stereoisomerism

2011
Catalytic highly enantioselective vinylogous Povarov reaction.
    Chemical communications (Cambridge, England), 2013, Jan-30, Volume: 49, Issue:9

    Topics: Butadienes; Catalysis; Phosphoric Acids; Quinolines; Stereoisomerism

2013
A highly diastereo- and enantioselective synthesis of tetrahydroquinolines: quaternary stereogenic center inversion and functionalization.
    Journal of the American Chemical Society, 2013, Jun-05, Volume: 135, Issue:22

    Topics: Catalysis; Cyclization; Molecular Structure; Phosphoric Acids; Quinolines; Stereoisomerism

2013
Facile construction of three contiguous stereogenic centers via dynamic kinetic resolution in asymmetric transfer hydrogenation of quinolines.
    Chemical communications (Cambridge, England), 2014, Oct-25, Volume: 50, Issue:83

    Topics: Catalysis; Crystallography, X-Ray; Hydrogen; Hydrogenation; Kinetics; Models, Molecular; Phosphoric Acids; Quinolines; Stereoisomerism

2014
Chiral phosphoric acid catalyzed oxidative kinetic resolution of cyclic secondary amine derivatives including tetrahydroquinolines by hydrogen transfer to imines.
    Chemical communications (Cambridge, England), 2015, Dec-04, Volume: 51, Issue:93

    Topics: Amines; Catalysis; Hydrogen; Imines; Kinetics; Molecular Structure; Oxidation-Reduction; Phosphoric Acids; Quinolines

2015