1292849-59-2Relevant academic research and scientific papers
Atroposelective formation of dibenz[c,e]azepines via intramolecular direct arylation with centre-axis chirality transfer
Cheetham, Caroline A.,Massey, Richard S.,Pira, Silvain L.,Pritchard, Robin G.,Wallace, Timothy W.
, p. 1831 - 1838 (2011/04/26)
5-Substituted 6,7-dihydrodibenz[c,e]azepines, a class of secondary amine incorporating a centre-axis chirality relay, are accessible from 1-substituted N-(2-bromobenzyl)-1-phenylmethanamines via N-acylation and ring-closing intramolecular direct arylation. The ring closure proceeds with high atropodiastereoselectivity due to strain effects that are induced by trigonalisation of the nitrogen atom, as predicted using molecular mechanics calculations.
