@article {49643,
	title = {Organocatalyzed [4+2] cycloaddition of α,β-unsaturated ketones and isatylidene malononitrile: accessing spiro[3-arylcyclohexanone]oxindole derivatives},
	journal = {RSC Advances},
	volume = {14},
	year = {2024},
	month = {JAN},
	pages = {2873-2877},
	type = {Article},
	abstract = {<p>
	Herein, we developed a series of compounds featuring spiro[3-arylcyclohexanone]oxindoles through Barbas [4 + 2] cycloaddition reactions between isatylidene malononitrile and alpha,beta-unsaturated ketones using l-proline as an organocatalyst. The reported methodology offers many advantages such as mild reaction conditions, diverse substrate scope with high yields, easy reaction setup, and use of easily synthesizable starting materials. An l-proline catalyzed-Barbas-[4 + 2]-cycloaddition reaction is reported for the synthesis of spiro[3-arylcyclohexanone]oxindole derivatives. The method can tolerate a diverse substrate scope with high yields.</p>
},
	doi = {10.1039/d3ra07652k},
	author = {Patil, Baliram R. and Nichinde, Chandrakant B. and Chaudhari, Suryakant S. and Krishna, Gamidi Rama and Kinage, Anil K.}
}
