APA (7th ed.) Citation

L, M., P, Z., T, K., L, H., TP, B., & B, E. (2025). Iodine-promoted oxidative cross-coupling for the synthesis of (E)-2-(3-oxo-3-phenylprop-1-en-1-yl)-3-phenylquinazolin-4(3H)-one via C-H activation: Development of synthetic TLX agonists. Organic & biomolecular chemistry, 23(31), 7298. https://doi.org/10.1039/d5ob00672d

Chicago Style (17th ed.) Citation

L, Maram, Zhao P, Koelblen T, Hegazy L, Burris TP, and Elgendy B. "Iodine-promoted Oxidative Cross-coupling for the Synthesis of (E)-2-(3-oxo-3-phenylprop-1-en-1-yl)-3-phenylquinazolin-4(3H)-one via C-H Activation: Development of Synthetic TLX Agonists." Organic & Biomolecular Chemistry 23, no. 31 (2025): 7298. https://doi.org/10.1039/d5ob00672d.

MLA (9th ed.) Citation

L, Maram, et al. "Iodine-promoted Oxidative Cross-coupling for the Synthesis of (E)-2-(3-oxo-3-phenylprop-1-en-1-yl)-3-phenylquinazolin-4(3H)-one via C-H Activation: Development of Synthetic TLX Agonists." Organic & Biomolecular Chemistry, vol. 23, no. 31, 2025, p. 7298, https://doi.org/10.1039/d5ob00672d.