Cite
Tandem Aza-Michael and Intramolecular Amidic Ring-Opening Reactions of ß-Lactams: A Facile Synthesis of 4-Oxo-4,5-dihydro-1H-pyrroles from ß-Lactam Synthons.
MLA
Sharma, Priyanka, et al. “Tandem Aza-Michael and Intramolecular Amidic Ring-Opening Reactions of ß-Lactams: A Facile Synthesis of 4-Oxo-4,5-Dihydro-1H-Pyrroles from ß-Lactam Synthons.” Synlett, vol. 27, no. 3, Feb. 2016, pp. 422–25. EBSCOhost, https://doi.org/10.1055/s-0035-1560826.
APA
Sharma, P., Mann, M. J. K., Kuila, B., Singh, P., & Bhargava, G. (2016). Tandem Aza-Michael and Intramolecular Amidic Ring-Opening Reactions of ß-Lactams: A Facile Synthesis of 4-Oxo-4,5-dihydro-1H-pyrroles from ß-Lactam Synthons. Synlett, 27(3), 422–425. https://doi.org/10.1055/s-0035-1560826
Chicago
Sharma, Priyanka, Maninder Jeet Kaur Mann, Bilash Kuila, Prabhpreet Singh, and Gaurav Bhargava. 2016. “Tandem Aza-Michael and Intramolecular Amidic Ring-Opening Reactions of ß-Lactams: A Facile Synthesis of 4-Oxo-4,5-Dihydro-1H-Pyrroles from ß-Lactam Synthons.” Synlett 27 (3): 422–25. doi:10.1055/s-0035-1560826.