APA (7th ed.) Citation

Campolo, D., Gaudel-Siri, A., Mondal, S., Siri, D., Besson, E., Vanthuyne, N., . . . Bertrand, M. P. (2012). Mechanistic Investigation of Enediyne-Connected Amino Ester Rearrangement. Theoretical Rationale for the Exclusive Preference for 1,6- or 1,5-Hydrogen Atom Transfer Depending on the Substrate. A Potential Route to Chiral Naphthoazepines. Journal of Organic Chemistry, 77(6), 2773. https://doi.org/10.1021/jo202580y

Chicago Style (17th ed.) Citation

Campolo, Damien, Anouk Gaudel-Siri, Shovan Mondal, Didier Siri, Eric Besson, Nicolas Vanthuyne, Malek Nechab, and Michele P. Bertrand. "Mechanistic Investigation of Enediyne-Connected Amino Ester Rearrangement. Theoretical Rationale for the Exclusive Preference for 1,6- or 1,5-Hydrogen Atom Transfer Depending on the Substrate. A Potential Route to Chiral Naphthoazepines." Journal of Organic Chemistry 77, no. 6 (2012): 2773. https://doi.org/10.1021/jo202580y.

MLA (9th ed.) Citation

Campolo, Damien, et al. "Mechanistic Investigation of Enediyne-Connected Amino Ester Rearrangement. Theoretical Rationale for the Exclusive Preference for 1,6- or 1,5-Hydrogen Atom Transfer Depending on the Substrate. A Potential Route to Chiral Naphthoazepines." Journal of Organic Chemistry, vol. 77, no. 6, 2012, p. 2773, https://doi.org/10.1021/jo202580y.