@article { ISI:000339367300057,
	title = {Transition-metal-free C-S bond formation: a facile access to aryl sulfones from sodium sulfinates via arynes},
	journal = {Organic Letters},
	volume = {16},
	number = {14},
	year = {2014},
	month = {JUL},
	pages = {3836-3839},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>Sulfones have been attractive targets for synthetic organic chemists owing to their immense applications in medicinal, material, and synthetic chemistry. In this context, an efficient transition-metal-free process has been demonstrated, wherein a broad range of alkyl/aryl/heteroaryl sodium sulfinates react with varyingly substituted aryne precursors (o-silyl aryl triflates) under mild reaction conditions to afford structurally diverse sulfones in good to excellent yields.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol5018646},
	author = {Pandya, Virat G. and Mhaske, Santosh B.}
}
@article {44454,
	title = {Divergent synthesis of oxindolylidene acetates and spirooxindolopyrrolidones from arynes},
	journal = {Organic Letters},
	volume = {20},
	year = {2018},
	month = {MAR},
	pages = {1483-1486},
	abstract = {A novel process for the preparation of various (E)-oxindolylidene acetates using arynes and carbamoylpropiolates has been developed. The utility of this protocol is also further extended to the one-pot synthesis of complex spirooxindolopyrrolidones. This method provides a milder and transition-metal-free access to both of the target scaffolds in moderate to good yields.},
	doi = {10.1021/acs.orglett.7b03661},
	author = {Pandya, Virat G. and Mhaske, Santosh B.}
}
@article {48030,
	title = {Construction of tetrahydrobenzo[f]quinoline scaffolds via polar [4+2]-Cycloaddition reaction with arynes as dienophiles},
	journal = {Tetrahedron Letters},
	volume = {101},
	year = {2022},
	month = {JUL},
	pages = {153901},
	type = {Article},
	abstract = {<p>
	A transition-metal-free route has been developed for the direct synthesis of biologically significant tetrahydrobenzo[f]quinoline scaffolds. The reaction features polar [4 + 2] Diels-Alder cycloaddition reaction of arynes with a well-designed diene N-Boc protected vinyl tetrahydropyridine, followed by the isomerisation of the double bond leading to the formation of tetrahydrobenzo[f]quinoline scaffolds in good to moderate yields.</p>
},
	keywords = {Aryne, Diels-Alder, Diene, Tetrahydrobenzo[ f ]quinoline},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2022.153901},
	author = {Pandya, Virat G. and Mhaske, Santosh B.}
}
