Nucleophilic and electrophilic double aroylation of chalcones with benzils promoted by the dimsyl anion as a route to all carbon tetrasubstituted olefins.

MLA

Ragno, Daniele, et al. “Nucleophilic and Electrophilic Double Aroylation of Chalcones with Benzils Promoted by the Dimsyl Anion as a Route to All Carbon Tetrasubstituted Olefins.” The Journal of Organic Chemistry, vol. 80, no. 3, Feb. 2015, pp. 1937–45. EBSCOhost, https://doi.org/10.1021/jo502582e.

APA

Ragno, D., Bortolini, O., Fantin, G., Fogagnolo, M., Giovannini, P. P., & Massi, A. (2015). Nucleophilic and electrophilic double aroylation of chalcones with benzils promoted by the dimsyl anion as a route to all carbon tetrasubstituted olefins. The Journal of Organic Chemistry, 80(3), 1937–1945. https://doi.org/10.1021/jo502582e

Chicago

Ragno, Daniele, Olga Bortolini, Giancarlo Fantin, Marco Fogagnolo, Pier Paolo Giovannini, and Alessandro Massi. 2015. “Nucleophilic and Electrophilic Double Aroylation of Chalcones with Benzils Promoted by the Dimsyl Anion as a Route to All Carbon Tetrasubstituted Olefins.” The Journal of Organic Chemistry 80 (3): 1937–45. doi:10.1021/jo502582e.