1040531-72-3Relevant articles and documents
Photoassisted diversity-oriented synthesis: Accessing 2,6-epoxyazocane (oxamorphan) cores
Mukhina, Olga A.,Kumar, N. N. Bhuvan,Cowger, Teresa M.,Kutateladze, Andrei G.
, p. 10956 - 10971 (2014)
The modular synthesis of photoprecursors and their photoinduced cyclization into substituted 1-benzazocanes of two distinct topologies is described. The key step producing an extended polyheterocyclic system involves the photogeneration of azaxylylenes and their subsequent intramolecular cycloaddition with furan-containing pendants tethered either via the aniline nitrogen or through the carbonyl group containing arm. The primary photoproducts-secondary or tertiary anilines which are not acylated at the nitrogen atom-undergo facile acid-catalyzed or spontaneous ring-opening-ring-closing rearrangement to yield fused polyheterocyclic structures possessing a 2,6-epoxyazocane (or oxamorphan) core.
