Paquette, L. A., Underiner, T. L., & Gallucci, J. C. (1992). Structural analysis of cis-[n.3.1]bicyclic ketones by x-ray crystallography. Impact of the observed conformational crossover by .pi.-facially diastereoselective nucleophilic additions to this class of ketones and on the stereochemical course of electrophilic reactions involving their methylene analogs. Journal of organic chemistry, 57(1), 86-96. https://doi.org/10.1021/jo00027a018
Chicago Style (17th ed.) CitationPaquette, Leo A., Ted L. Underiner, and Judith C. Gallucci. "Structural Analysis of Cis-[n.3.1]bicyclic Ketones by X-ray Crystallography. Impact of the Observed Conformational Crossover by .pi.-facially Diastereoselective Nucleophilic Additions to This Class of Ketones and on the Stereochemical Course of Electrophilic Reactions Involving Their Methylene Analogs." Journal of Organic Chemistry 57, no. 1 (1992): 86-96. https://doi.org/10.1021/jo00027a018.
MLA (9th ed.) CitationPaquette, Leo A., et al. "Structural Analysis of Cis-[n.3.1]bicyclic Ketones by X-ray Crystallography. Impact of the Observed Conformational Crossover by .pi.-facially Diastereoselective Nucleophilic Additions to This Class of Ketones and on the Stereochemical Course of Electrophilic Reactions Involving Their Methylene Analogs." Journal of Organic Chemistry, vol. 57, no. 1, 1992, pp. 86-96, https://doi.org/10.1021/jo00027a018.