Cite
7-Endo-trig Pictet–Spengler type cyclization of 5-alkylidene/arylidene-amino-3H-pyrimidin-4-ones: An efficient and diastereoselective synthesis of pyrimido[4,5-b] [1,4]benzodiazepines.
MLA
Naikoo, Rayees Ahmad, et al. “7-Endo-Trig Pictet–Spengler Type Cyclization of 5-Alkylidene/Arylidene-Amino-3H-Pyrimidin-4-Ones: An Efficient and Diastereoselective Synthesis of Pyrimido[4,5-b] [1,4]Benzodiazepines.” Synthetic Communications, vol. 51, no. 8, Apr. 2021, pp. 1232–41. EBSCOhost, https://doi.org/10.1080/00397911.2021.1878224.
APA
Naikoo, R. A., Kumar, R., Singh, P., & Bhargava, G. (2021). 7-Endo-trig Pictet–Spengler type cyclization of 5-alkylidene/arylidene-amino-3H-pyrimidin-4-ones: An efficient and diastereoselective synthesis of pyrimido[4,5-b] [1,4]benzodiazepines. Synthetic Communications, 51(8), 1232–1241. https://doi.org/10.1080/00397911.2021.1878224
Chicago
Naikoo, Rayees Ahmad, Rupesh Kumar, Parvesh Singh, and Gaurav Bhargava. 2021. “7-Endo-Trig Pictet–Spengler Type Cyclization of 5-Alkylidene/Arylidene-Amino-3H-Pyrimidin-4-Ones: An Efficient and Diastereoselective Synthesis of Pyrimido[4,5-b] [1,4]Benzodiazepines.” Synthetic Communications 51 (8): 1232–41. doi:10.1080/00397911.2021.1878224.