@article {49353,
	title = {Modular synthesis of unsymmetrical indolyl diketones from ynediones via sequential aza-Michael addition/C-H functionalization},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {22},
	year = {2024},
	month = {OCT },
	pages = {8152-8156},
	type = {Article},
	abstract = {<p>
	Herein, we disclose an efficient approach for the synthesis of unsymmetrical indolyl diketones from easily accessible 1,2-alkynediones involving a sequential aza-Michael addition/C-H Functionalization process. The two-step, one-pot strategy involves the aza-Michael addition of an aniline generating the N-aryl enaminones followed by iodine-mediated C-H functionalization.</p>
},
	issn = {1477-0520},
	doi = {10.1039/d4ob00946k},
	author = {Naveed, Abdul and Bag, Debojyoti and Sawant, Sanghapal D.}
}
