193977-54-7Relevant academic research and scientific papers
Stereoselective synthesis of the 2,6-disubstituted tetrahydropyran-3-ol of the potent antitumor agent mucocin via an acyl radical cyclization
Evans, P. Andrew,Roseman, Jamie D.
, p. 5249 - 5252 (2007/10/03)
The intramolecular acyl radical cyclization of the acyl selenide 8, using a Z-vinylogous sulfonate to control rotamer population, affords the cis-2,6-disubstituted tetrahydropyran-4-one 9, applicable to the potent antitumor agent mucocin 1 in 81% yield.
