The Acidity of a Carbon Nucleophile Dictates Enantioselectivity and Reactivity in Michael Additions to Aromatic and Aliphatic Enals via Iminium Activation

MLA

Inés Alonso, et al. The Acidity of a Carbon Nucleophile Dictates Enantioselectivity and Reactivity in Michael Additions to Aromatic and Aliphatic Enals via Iminium Activation. Jan. 2017. 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.dedup.....ddc7a38c4f2e8dfe6decb5120267eed7&authtype=sso&custid=ns315887.

APA

Inés Alonso, Eduardo Rodrigo, José L. García Ruano, Sara Duce, Ana Poveda, Al Mokhtar Lamsabhi, Pablo Mauleón, Sara Morales, & M. Belén Cid. (2017). The Acidity of a Carbon Nucleophile Dictates Enantioselectivity and Reactivity in Michael Additions to Aromatic and Aliphatic Enals via Iminium Activation.

Chicago

Inés Alonso, Eduardo Rodrigo, José L. García Ruano, Sara Duce, Ana Poveda, Al Mokhtar Lamsabhi, Pablo Mauleón, Sara Morales, and M. Belén Cid. 2017. “The Acidity of a Carbon Nucleophile Dictates Enantioselectivity and Reactivity in Michael Additions to Aromatic and Aliphatic Enals via Iminium Activation,” January. 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.dedup.....ddc7a38c4f2e8dfe6decb5120267eed7&authtype=sso&custid=ns315887.