1553422-66-4Relevant academic research and scientific papers
Intermolecular (4+3) cycloadditions of aziridinyl enolsilanes
Lam, Sze Kui,Lam, Sarah,Wong, Wing-Tak,Chiu, Pauline
, p. 1738 - 1741 (2014/02/14)
Upon activation by strong Bronsted acids, aziridinyl enolsilanes undergo (4+3) cycloadditions with dienes to afford aminoalkylated cycloheptenones as products. The use of a highly polar medium such as nitroalkane facilitates high cycloaddition yields of up to 99%. Optically pure aziridinyl enolsilanes react to yield (4+3) cycloadducts with up to 99% ee.
