934016-05-4Relevant academic research and scientific papers
Highly diastereoselective radical cyclisations of chiral sulfinimines
Rochette, Elise M.,Lewis, William,Dossetter, Al G.,Stockman, Robert A.
, p. 9395 - 9397 (2013/10/01)
Chiral amines are formed by the highly diastereoselective intramolecular addition of alkyl and aryl radicals onto chiral mesityl sulfinimines.
Carbocyclization by radical closure onto O-trityl oximes: Dramatic effect of diphenyl diselenide
Clive, Derrick L. J.,Pham, Mai P.,Subedi, Rajendra
, p. 2713 - 2717 (2007/10/03)
O-Trityl oximes of 5- and 6-iodoaldehydes undergo radical cyclization to produce oximes when treated in refluxing tetrahydrofuran (THF) with Bu 3SnH, 1,1′-azobis(cyclohexanecarbonitrile), i-Pr 2NEt, and diphenyl diselenide (PhSeSePh).
