Pu, Youge, Smaldone, Anthony M, Adrio, Javier, and Walsh, Patrick J. Sulfenate Anion Catalyzed Enantio- and Diastereoselective Aziridination. Retrieved from https://par.nsf.gov/biblio/10634709. Chemical Science . Web. doi:10.1039/D5SC05077D.

Pu, Youge, Smaldone, Anthony M, Adrio, Javier, & Walsh, Patrick J. Sulfenate Anion Catalyzed Enantio- and Diastereoselective Aziridination. Chemical Science, (). Retrieved from https://par.nsf.gov/biblio/10634709. https://doi.org/10.1039/D5SC05077D

Pu, Youge, Smaldone, Anthony M, Adrio, Javier, and Walsh, Patrick J. "Sulfenate Anion Catalyzed Enantio- and Diastereoselective Aziridination". Chemical Science (). Country unknown/Code not available: RCS. https://doi.org/10.1039/D5SC05077D. https://par.nsf.gov/biblio/10634709.

@article{osti_10634709,
place = {Country unknown/Code not available}, title = {Sulfenate Anion Catalyzed Enantio- and Diastereoselective Aziridination}, url = {https://par.nsf.gov/biblio/10634709}, DOI = {10.1039/D5SC05077D}, abstractNote = {The synthesis of enantioenriched aziridines is important for drug development due to their prevalence in bioactive molecules. Previous methods often use expensive catalysts, activated substrates, or show poor stereoselectivity. Herein,...}, journal = {Chemical Science}, publisher = {RCS}, author = {Pu, Youge and Smaldone, Anthony M and Adrio, Javier and Walsh, Patrick J}, }