457646-59-2Relevant academic research and scientific papers
Studies in sigmatropic rearrangement: Synthesis of a [6,6]pyranothiopyran ring system by sequential claisen rearrangement and pyridine hydrotribromide mediated regioselective "6-Endo"cyclization
Majumdar,Kundu,Ghosh
, p. 2629 - 2631 (2007/10/03)
(Matrix presented) 4-(4′-Aryloxybut-2′-ynylthio)[1]benzopyran-2-ones are refluxed in chlorobenzene to afford 4-aryloxymethylthiopyrano[3,2-c][1]benzopyran-5(2H)-ones which are subsequently subjected to heating in o-dichlorobenzene in the presence of N,N-d
