@article {47625,
	title = {Intermolecular interception of alpha-oxo gold carbenes of nitroalkyne cycloisomerization with 1, 2-benzo[d]isoxazole: synthesis of functionalized quinazoline 1-oxides},
	journal = {Journal of Organic Chemistry},
	volume = {86},
	year = {2021},
	month = {AUG },
	pages = {10874-10882},
	type = {Article},
	abstract = {The known nitrogen-transfer reagent 1,2-benzo[d]isoxazole has been used to trap the postulated a-oxo gold carbene intermediate involved in the [Au]-catalyzed internal redox process of 2-alkynylnitrobenzenes. This process led us to develop a general convergent method for the synthesis of highly functionalized quinazoline 1-oxides.},
	issn = {0022-3263},
	doi = {10.1021/acs.joc.1c01221},
	author = {Dhote, Pawan S. and Pund, Kishor A. and Ramana, V, Chepuri}
}
@article {47407,
	title = {Interrupting the [Au]-catalyzed nitroalkyne cycloisomerization: trapping the putative alpha-oxo gold carbene with benzo[c]isoxazole},
	journal = {Organic Letters},
	volume = {23},
	year = {2021},
	month = {APR },
	pages = {2632-2637},
	type = {Article},
	abstract = {<p>The [Au]-catalyzed nitroalkyne cycloisomerization of 2-alkynylnitrobenzenes leading to anthranils has been interrupted by possible trapping of the postulated intermediate alpha-oxo gold carbene with an external nucleophile such as benzo[c]isoxazole (anthranil). At the outset, this provides a simple synthesis of highly functionalized 3-acyl-(2-formylphenyl)-2H-indazoles with the sequential C-O, C-N, and N-N bond formations. This provides indirect support for the existence of alpha-oxo gold carbenes in the [Au]-catalyzed internal redox processes of nitroalkynes.</p>},
	issn = {1523-7060},
	doi = {10.1021/acs.orglett.1c00539},
	author = {Dhote, Pawan S. and Ramana, V, Chepuri}
}
