@article {49399,
	title = {Manganese-mediated cascade radical oxidative cyclization/1,6-conjugate addition of unsaturated oximes with p-quinone methides: facile access to β,β-diarylmethine substituted isoxazolines},
	journal = {Chemistry-An Asian Journal},
	year = {2024},
	month = {NOV},
	type = {Article; Early Access},
	abstract = {<p>
	A simple and efficient strategy for the synthesis of structurally diverse beta,beta-diarylmethine substituted isoxazoline derivatives have been developed. This approach employs a manganese-promoted oxidative cyclization coupled with a 1,6-conjugate addition of unsaturated oximes to p-quinone methides. The key features of this study include the formation of C-O and C-C bonds through intramolecular and intermolecular interactions, facilitated by in situ generated iminoxyl radicals. beta,beta-diarylmethine substituted isoxazolines, bearing a wide range of functional groups, were isolated in high yields.</p>
},
	keywords = {<italic>p</italic>-Quinone methide, diarylmethine substituted isoxazolines, Iminoxy radical, Manganese catalyzed},
	issn = {1861-4728},
	doi = {10.1002/asia.202401079},
	author = {Vara, Vijay and Thete, Kishor R. and Ghotekar, Ganesh S. and Muthukrishnan, M.}
}
