Cite
Deacylative alkylation (DaA) of N-methyl-3-acetyl-2-oxindole for the synthesis of symmetrically 3,3-disubstituted 2-oxindoles. An access gate to anticancer agents and natural products
MLA
Universidad de Alicante. Departamento de Química Orgánica, et al. Deacylative Alkylation (DaA) of N-Methyl-3-Acetyl-2-Oxindole for the Synthesis of Symmetrically 3,3-Disubstituted 2-Oxindoles. An Access Gate to Anticancer Agents and Natural Products. 2018. 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=edsoai&AN=edsoai.on1049561626&authtype=sso&custid=ns315887.
APA
Universidad de Alicante. Departamento de Química Orgánica, Universidad de Alicante. Instituto Universitario de Síntesis Orgánica, Moreno-Cabrerizo, C., Ortega-Martínez, A., Molina, C., Nájera, C., & Sansano, J. M. (2018). Deacylative alkylation (DaA) of N-methyl-3-acetyl-2-oxindole for the synthesis of symmetrically 3,3-disubstituted 2-oxindoles. An access gate to anticancer agents and natural products.
Chicago
Universidad de Alicante. Departamento de Química Orgánica, Universidad de Alicante. Instituto Universitario de Síntesis Orgánica, Cristina Moreno-Cabrerizo, Aitor Ortega-Martínez, Cynthia Molina, Carmen Nájera, and Jose M. Sansano. 2018. “Deacylative Alkylation (DaA) of N-Methyl-3-Acetyl-2-Oxindole for the Synthesis of Symmetrically 3,3-Disubstituted 2-Oxindoles. An Access Gate to Anticancer Agents and Natural Products.” 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=edsoai&AN=edsoai.on1049561626&authtype=sso&custid=ns315887.