Study of the Cis to Trans Isomerization of 1-Phenyl-2,3-disubstituted Tetrahydro-β-carbolines at C(1). Evidence for the Carbocation-Mediated Mechanism.

MLA

Kumpaty, Hephzibah J., et al. “Study of the Cis to Trans Isomerization of 1-Phenyl-2,3-Disubstituted Tetrahydro-β-Carbolines at C(1). Evidence for the Carbocation-Mediated Mechanism.” Journal of Organic Chemistry, vol. 74, no. 7, Apr. 2009, pp. 2771–79. EBSCOhost, https://doi.org/10.1021/jo8028168.

APA

Kumpaty, H. J., Van Linn, M. L., Kabir, M. S., Forsterling, F. H., Deschamps, J. R., & Cook, J. M. (2009). Study of the Cis to Trans Isomerization of 1-Phenyl-2,3-disubstituted Tetrahydro-β-carbolines at C(1). Evidence for the Carbocation-Mediated Mechanism. Journal of Organic Chemistry, 74(7), 2771–2779. https://doi.org/10.1021/jo8028168

Chicago

Kumpaty, Hephzibah J., Michael L. Van Linn, M. Shahjahan Kabir, F. Holger Forsterling, Jeffrey R. Deschamps, and James M. Cook. 2009. “Study of the Cis to Trans Isomerization of 1-Phenyl-2,3-Disubstituted Tetrahydro-β-Carbolines at C(1). Evidence for the Carbocation-Mediated Mechanism.” Journal of Organic Chemistry 74 (7): 2771–79. doi:10.1021/jo8028168.