APA

Callis D. J., Thomas N. F., Pearson D. P. J. & Potter B. V. L. (1996). A Tandem Horner-Emmons Olefination-Conjugate Addition Approach to the Synthesis of 1,5-Disubstituted-6-azabicyclo[3.2.1]octanes Based on the AE Ring Structure of the Norditerpenoid Alkaloid Methyllycaconitine. : The Journal of organic chemistry.

Chicago

Callis David J, Thomas Noel F, Pearson David P J and Potter Barry V L. 1996. A Tandem Horner-Emmons Olefination-Conjugate Addition Approach to the Synthesis of 1,5-Disubstituted-6-azabicyclo[3.2.1]octanes Based on the AE Ring Structure of the Norditerpenoid Alkaloid Methyllycaconitine. : The Journal of organic chemistry.

Harvard

Callis D. J., Thomas N. F., Pearson D. P. J. and Potter B. V. L. (1996). A Tandem Horner-Emmons Olefination-Conjugate Addition Approach to the Synthesis of 1,5-Disubstituted-6-azabicyclo[3.2.1]octanes Based on the AE Ring Structure of the Norditerpenoid Alkaloid Methyllycaconitine. : The Journal of organic chemistry.

MLA

Callis David J, Thomas Noel F, Pearson David P J and Potter Barry V L. A Tandem Horner-Emmons Olefination-Conjugate Addition Approach to the Synthesis of 1,5-Disubstituted-6-azabicyclo[3.2.1]octanes Based on the AE Ring Structure of the Norditerpenoid Alkaloid Methyllycaconitine. : The Journal of organic chemistry. 1996.