Abstract
Ultraviolet irradiation of
(+)-glaucine methiodide in methanol gave the elimination product 1-[2'-(N,N-dimethylaminoethyl)]-3,4,6,7-
tetramethoxyphenanthrene in good yield. Analogous
products were obtained from the ethiodide and benzylbromide salts of this
aporphine alkaloid, and from quaternary salts of (+)-boldine and (-)-O,O'-dimethylapomorphine.
This photoelimination reaction was also applied to the hydrochloride salts of
(+)-glaucine and (+)-boldine.
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