Development of Kinase Inhibitors via Metal-Catalyzed C-H Arylation of 8-Alkyl-thiazolo[5,4-f]-quinazolin-9-ones Designed by Fragment-Growing Studies.

MLA

Couly, Florence, et al. “Development of Kinase Inhibitors via Metal-Catalyzed C-H Arylation of 8-Alkyl-Thiazolo[5,4-f]-Quinazolin-9-Ones Designed by Fragment-Growing Studies.” Molecules, vol. 23, no. 9, Sept. 2018, p. 2181. EBSCOhost, https://doi.org/10.3390/molecules23092181.

APA

Couly, F., Harari, M., Dubouilh-Benard, C., Bailly, L., Petit, E., Diharce, J., Bonnet, P., Meijer, L., Fruit, C., & Besson, T. (2018). Development of Kinase Inhibitors via Metal-Catalyzed C-H Arylation of 8-Alkyl-thiazolo[5,4-f]-quinazolin-9-ones Designed by Fragment-Growing Studies. Molecules, 23(9), 2181. https://doi.org/10.3390/molecules23092181

Chicago

Couly, Florence, Marine Harari, Carole Dubouilh-Benard, Laetitia Bailly, Emilie Petit, Julien Diharce, Pascal Bonnet, Laurent Meijer, Corinne Fruit, and Thierry Besson. 2018. “Development of Kinase Inhibitors via Metal-Catalyzed C-H Arylation of 8-Alkyl-Thiazolo[5,4-f]-Quinazolin-9-Ones Designed by Fragment-Growing Studies.” Molecules 23 (9): 2181. doi:10.3390/molecules23092181.