@article {46686,
	title = {Oxidative rearrangement of stilbenes to 2,2-diaryl-2-hydroxyacetaldehydes},
	journal = {ACS Omega},
	volume = {5},
	year = {2020},
	month = {OCT },
	pages = {25199-25208},
	type = {Article},
	abstract = {<p>A one-pot oxone-mediated/iodine-catalyzed oxidative rearrangement of stilbenes leading to 2,2-diary1-2-hydroxyacetaldehydes is described. Control experiments revealed that a 2,2-diarylacetaldehyde was initially formed that undergoes subsequent alpha-hydroxylation. The resulting alpha-hydroxyaldehydes have been subjected to a one-pot Still Gennari olefination followed by cyclization, leading to S,S-diaryl-y-butenolides.</p>
},
	issn = {2470-1343},
	doi = {10.1021/acsomega.0c03328},
	author = {Kalshetti, Rupali G. and Ramana, V. Chepuri}
}
