@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.}
}
