Cite
Catalyst-free and oxidant-free tandem aza-Mannich/cyclization/aromatization of C,N-cyclic azomethine imines with enamides: facile synthesis of 5,6-dihydropyrazolo[5,1-a]isoquinolines.
MLA
Dong, Hao, et al. “Catalyst-Free and Oxidant-Free Tandem Aza-Mannich/Cyclization/Aromatization of C,N-Cyclic Azomethine Imines with Enamides: Facile Synthesis of 5,6-Dihydropyrazolo[5,1-a]Isoquinolines.” Green Chemistry, vol. 24, no. 14, July 2022, pp. 5508–13. EBSCOhost, https://doi.org/10.1039/d2gc01275h.
APA
Dong, H., Zhang, Y., Tian, X., Pang, R., Ren, W., & Wang, Y. (2022). Catalyst-free and oxidant-free tandem aza-Mannich/cyclization/aromatization of C,N-cyclic azomethine imines with enamides: facile synthesis of 5,6-dihydropyrazolo[5,1-a]isoquinolines. Green Chemistry, 24(14), 5508–5513. https://doi.org/10.1039/d2gc01275h
Chicago
Dong, Hao, Yongxing Zhang, Xiaochen Tian, Ruochen Pang, Weiwu Ren, and Yang Wang. 2022. “Catalyst-Free and Oxidant-Free Tandem Aza-Mannich/Cyclization/Aromatization of C,N-Cyclic Azomethine Imines with Enamides: Facile Synthesis of 5,6-Dihydropyrazolo[5,1-a]Isoquinolines.” Green Chemistry 24 (14): 5508–13. doi:10.1039/d2gc01275h.