1062096-76-7Relevant academic research and scientific papers
Chiral azabicyclo-N-oxyls mediated enantioselective electrooxidation of sec-alcohols
Shiigi, Hirofumi,Mori, Hiroyuki,Tanaka, Tomoaki,Demizu, Yosuke,Onomura, Osamu
, p. 5247 - 5251 (2008/12/22)
Enantiomerically pure azabicyclo-N-oxyls were prepared from l-hydroxyproline. They mediated enantioselective electrooxidation of racemic sec-alcohols to afford optically active sec-alcohols with moderate to high s value (up to 21).
