Application of Photoamination to Synthesis of Benzylisoquinolines, Aporphins, and Isopavines
摘要:
The preparation of benzylisoquinolines, isopavines, and aporphines was performed by the photoamination of stilbene, p-methoxystilbene, and phenanthrene with amino alcohols, aminoacetal, allylamine in the presence of dicyanobenzene followed by the cyclization with BF3 or CF3SO3H.
The preparation of benzylisoquinolines, isopavines, and aporphines was performed by the photoamination of stilbene, p-methoxystilbene, and phenanthrene with amino alcohols, aminoacetal, allylamine in the presence of dicyanobenzene followed by the cyclization with BF3 or CF3SO3H.
Babayan,A.T. et al., Journal of general chemistry of the USSR, 1963, vol. 33, p. 1727 - 1731