High-Pressure-Promoted and Facially Selective Diels–Alder Reactions of Enzymatically Derived cis-1,2-Dihydrocatechols and Their Acetonide Derivatives: Enantiodivergent Routes to Homochiral and Polyfunctionalized Bicyclo[2.2.2]octenes

MLA

Anthony C. Willis, et al. “High-Pressure-Promoted and Facially Selective Diels–Alder Reactions of Enzymatically Derived Cis-1,2-Dihydrocatechols and Their Acetonide Derivatives: Enantiodivergent Routes to Homochiral and Polyfunctionalized Bicyclo[2.2.2]Octenes.” The Journal of Organic Chemistry, vol. 85, Sept. 2020, pp. 13080–95. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi...........a233250bf505fa7f10c193785e832bd8&authtype=sso&custid=ns315887.

APA

Anthony C. Willis, Yinglai Teng, Roberto Cammi, Li-Juan Yu, Michelle L. Coote, Bo Chen, Scott G. Stewart, Martin G. Banwell, Gwion J. Harfoot, & Kenneth J. McRae. (2020). High-Pressure-Promoted and Facially Selective Diels–Alder Reactions of Enzymatically Derived cis-1,2-Dihydrocatechols and Their Acetonide Derivatives: Enantiodivergent Routes to Homochiral and Polyfunctionalized Bicyclo[2.2.2]octenes. The Journal of Organic Chemistry, 85, 13080–13095.

Chicago

Anthony C. Willis, Yinglai Teng, Roberto Cammi, Li-Juan Yu, Michelle L. Coote, Bo Chen, Scott G. Stewart, Martin G. Banwell, Gwion J. Harfoot, and Kenneth J. McRae. 2020. “High-Pressure-Promoted and Facially Selective Diels–Alder Reactions of Enzymatically Derived Cis-1,2-Dihydrocatechols and Their Acetonide Derivatives: Enantiodivergent Routes to Homochiral and Polyfunctionalized Bicyclo[2.2.2]Octenes.” The Journal of Organic Chemistry 85 (September): 13080–95. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi...........a233250bf505fa7f10c193785e832bd8&authtype=sso&custid=ns315887.