20565-99-5Relevant academic research and scientific papers
N-(trans-1-propenyl)carbazole: An excellent dienophile for cation radical Diels-Alder cycloadditions
Gao,Bauld
, p. 5997 - 6000 (2007/10/03)
The efficient, regiospecific, and periselective Diels-Alder cycloadditions of N-(trans-1-propenyl)carbazole, a highly electron rich dienophile, to both acyclic and cyclic conjugated dienes is found to be induced by tris(4-bromophenyl)aminium hexachloroantimonate. (C) 2000 Elsevier Science Ltd.
