1380499-76-2Relevant academic research and scientific papers
Acid-promoted rearrangement of arylmethyl azides: Applications toward the synthesis of N-arylmethyl arenes and polycyclic heteroaromatic compounds
Tummatorn, Jumreang,Thongsornkleeb, Charnsak,Ruchirawat, Somsak
, p. 4732 - 4739 (2012)
An acid-promoted Aubé-Schmidt's rearrangement of arylmethyl azides provides a useful in situ iminium ion intermediate, which can be efficiently trapped by various nucleophiles. We report here the reaction of this iminium ion with aromatic nucleophiles to
