Synthesis of Guaianolide Analogues with a Tunable α-Methylene−γ-lactam Electrophile and Correlating Bioactivity with Thiol Reactivity

MLA

Matthew E. Cuellar, et al. “Synthesis of Guaianolide Analogues with a Tunable α-Methylene−γ-Lactam Electrophile and Correlating Bioactivity with Thiol Reactivity.” Journal of Medicinal Chemistry, vol. 63, Nov. 2020, pp. 14951–78. EBSCOhost, https://doi.org/10.1021/acs.jmedchem.0c01464.

APA

Matthew E. Cuellar, Daniel P Dempe, Kay M. Brummond, Paul A. Jackson, John C. Widen, Katherine F. M. Jones, Michael A. Walters, Henry A M Schares, Francois Grillet, & Daniel A. Harki. (2020). Synthesis of Guaianolide Analogues with a Tunable α-Methylene−γ-lactam Electrophile and Correlating Bioactivity with Thiol Reactivity. Journal of Medicinal Chemistry, 63, 14951–14978. https://doi.org/10.1021/acs.jmedchem.0c01464

Chicago

Matthew E. Cuellar, Daniel P Dempe, Kay M. Brummond, Paul A. Jackson, John C. Widen, Katherine F. M. Jones, Michael A. Walters, Henry A M Schares, Francois Grillet, and Daniel A. Harki. 2020. “Synthesis of Guaianolide Analogues with a Tunable α-Methylene−γ-Lactam Electrophile and Correlating Bioactivity with Thiol Reactivity.” Journal of Medicinal Chemistry 63 (November): 14951–78. doi:10.1021/acs.jmedchem.0c01464.