Nucleophile-Mediated Ring Expansion of 5-Acyl-substituted 4-Mesyloxymethyl-1,2,3,4-tetrahydropyrimidin-2-ones in the Synthesis of 7-Membered Analogues of Biginelli Compounds and Related Heterocycles.

MLA

Fesenko, Anastasia A., et al. “Nucleophile-Mediated Ring Expansion of 5-Acyl-Substituted 4-Mesyloxymethyl-1,2,3,4-Tetrahydropyrimidin-2-Ones in the Synthesis of 7-Membered Analogues of Biginelli Compounds and Related Heterocycles.” Journal of Organic Chemistry, vol. 82, no. 15, Aug. 2017, pp. 8085–110. EBSCOhost, https://doi.org/10.1021/acs.joc.7b01348.

APA

Fesenko, A. A., Grigoriev, M. S., & Shutalev, A. D. (2017). Nucleophile-Mediated Ring Expansion of 5-Acyl-substituted 4-Mesyloxymethyl-1,2,3,4-tetrahydropyrimidin-2-ones in the Synthesis of 7-Membered Analogues of Biginelli Compounds and Related Heterocycles. Journal of Organic Chemistry, 82(15), 8085–8110. https://doi.org/10.1021/acs.joc.7b01348

Chicago

Fesenko, Anastasia A., Mikhail S. Grigoriev, and Anatoly D. Shutalev. 2017. “Nucleophile-Mediated Ring Expansion of 5-Acyl-Substituted 4-Mesyloxymethyl-1,2,3,4-Tetrahydropyrimidin-2-Ones in the Synthesis of 7-Membered Analogues of Biginelli Compounds and Related Heterocycles.” Journal of Organic Chemistry 82 (15): 8085–8110. doi:10.1021/acs.joc.7b01348.