@article {49074,
	title = {Electrochemically enabled (3+2) cycloaddition of unbiased alkenes and β-dicarbonyls},
	journal = {Chemical Communications},
	volume = {60},
	year = {2024},
	month = {MAY },
	pages = {5836-5839},
	type = {Article},
	abstract = {<p>
	A (3+2) cycloaddition between unbiased alkenes and 1,3-dicarbonyls is accomplished by judicious choice of electrode material and electrocatalyst to access dihydrofuran derivatives. A fluorinated porous carbon electrode with appropriate thickness governs unprecedented reactivity. This methodology eliminates the necessity for any stabilizing group within the alkene substrate. This is a rare example of the annulation of unbiased internal and terminal alkenes with cyclic and acyclic beta-dicarbonyls.</p>
},
	keywords = {1, 3-DICARBONYL COMPOUNDS, DIHYDROFURANS, FACILE SYNTHESIS},
	issn = {1359-7345},
	doi = {10.1039/d4cc01263a},
	author = {Suryawanshi, Sharad M. and Sahoo, Suman and Shaligram, Parth S. and Manna, Narugopal and Samanta, Ramesh C.}
}
