MS, H., OEP, S., CJ, C., & K, H. (2017). N-Alkylation and Aminohydroxylation of 2-Azidobenzenesulfonamide Gives a Pyrrolobenzothiadiazepine Precursor Whereas Attempted N-Alkylation of 2-Azidobenzamide Gives Benzotriazinones and Quinazolinones. ACS omega, 2(3), 1222. https://doi.org/10.1021/acsomega.7b00211
Chicago Style (17th ed.) CitationMS, Hamasharif, Smith OEP, Curran CJ, and Hemming K. "N-Alkylation and Aminohydroxylation of 2-Azidobenzenesulfonamide Gives a Pyrrolobenzothiadiazepine Precursor Whereas Attempted N-Alkylation of 2-Azidobenzamide Gives Benzotriazinones and Quinazolinones." ACS Omega 2, no. 3 (2017): 1222. https://doi.org/10.1021/acsomega.7b00211.
MLA (9th ed.) CitationMS, Hamasharif, et al. "N-Alkylation and Aminohydroxylation of 2-Azidobenzenesulfonamide Gives a Pyrrolobenzothiadiazepine Precursor Whereas Attempted N-Alkylation of 2-Azidobenzamide Gives Benzotriazinones and Quinazolinones." ACS Omega, vol. 2, no. 3, 2017, p. 1222, https://doi.org/10.1021/acsomega.7b00211.