Morita, N.;                     Yamashita, D.;                     Hashimoto, Y.;                     Tamura, O.    
        An Efficient Stereoselective Synthesis of cis-2,6-Disubstituted Tetrahydropyrans via Gold-Catalyzed Meyer–Schuster Rearrangement/Hydration/oxa-Michael Addition Sequence. Catalysts 2024, 14, 228.
    https://doi.org/10.3390/catal14040228
    AMA Style
    
                                Morita N,                                 Yamashita D,                                 Hashimoto Y,                                 Tamura O.        
                An Efficient Stereoselective Synthesis of cis-2,6-Disubstituted Tetrahydropyrans via Gold-Catalyzed Meyer–Schuster Rearrangement/Hydration/oxa-Michael Addition Sequence. Catalysts. 2024; 14(4):228.
        https://doi.org/10.3390/catal14040228
    
    Chicago/Turabian Style
    
                                Morita, Nobuyoshi,                                 Daichi Yamashita,                                 Yoshimitsu Hashimoto,                                 and Osamu Tamura.        
                2024. "An Efficient Stereoselective Synthesis of cis-2,6-Disubstituted Tetrahydropyrans via Gold-Catalyzed Meyer–Schuster Rearrangement/Hydration/oxa-Michael Addition Sequence" Catalysts 14, no. 4: 228.
        https://doi.org/10.3390/catal14040228
    
    APA Style
    
                                Morita, N.,                                 Yamashita, D.,                                 Hashimoto, Y.,                                 & Tamura, O.        
        
        (2024). An Efficient Stereoselective Synthesis of cis-2,6-Disubstituted Tetrahydropyrans via Gold-Catalyzed Meyer–Schuster Rearrangement/Hydration/oxa-Michael Addition Sequence. Catalysts, 14(4), 228.
        https://doi.org/10.3390/catal14040228