263840-07-9Relevant academic research and scientific papers
Radical cyclization of O-trityl oximino esters: A ring closure that preserves the oxime function
Clive, Derrick L. J.,Subedi, Rajendra
, p. 237 - 238 (2007/10/03)
O-Trityl oximino esters 1 undergo stannane-induced radical cyclization to regenerate an oxime function, affording oximino lactones 4; these can be converted into enamides (e.g. 11b), and such a transformation was used to make the natural product 14c.
