Lewis acid-catalysed nucleophilic opening of a bicyclic hemiaminal followed by ring contraction: Access to functionalized L-idonojirimycin derivatives.

MLA

Auberger, N., et al. “Lewis Acid-Catalysed Nucleophilic Opening of a Bicyclic Hemiaminal Followed by Ring Contraction: Access to Functionalized L-Idonojirimycin Derivatives.” Carbohydrate Research, vol. 472, Jan. 2019, pp. 65–71. EBSCOhost, https://doi.org/10.1016/j.carres.2018.11.008.

APA

Auberger, N., Onfroy, B., Fontelle, N., Foucart, Q., & Blériot, Y. (2019). Lewis acid-catalysed nucleophilic opening of a bicyclic hemiaminal followed by ring contraction: Access to functionalized L-idonojirimycin derivatives. Carbohydrate Research, 472, 65–71. https://doi.org/10.1016/j.carres.2018.11.008

Chicago

Auberger, N., B. Onfroy, N. Fontelle, Q. Foucart, and Y. Blériot. 2019. “Lewis Acid-Catalysed Nucleophilic Opening of a Bicyclic Hemiaminal Followed by Ring Contraction: Access to Functionalized L-Idonojirimycin Derivatives.” Carbohydrate Research 472 (January): 65–71. doi:10.1016/j.carres.2018.11.008.