Journal of Heterocyclic Chemistry p. 87 - 92 (1979)
Update date:2022-08-05
Topics:
Elmaleh
Granchelli
Neumeyer
The synthesis of three new racemic aporphine alkaloids [1b, 1c and N-n-propylnorisocorydine] is reported and these alkaloids are fully characterized. The method of synthesis involved either a Bischler-Napieralski-Pschorr sequence or a Reissert alkylation-Pschorr cyclization route. The Pschorr cyclization also gave the morphinandienones with an OH group and also with an OCH3 group, respectively.
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Doi:10.1039/p19960001461
(1996)Doi:10.1021/jo00337a011
(1981)Doi:10.1002/hlca.19790620414
(1979)Doi:10.1055/s-1979-28670
(1979)Doi:10.1002/jhet.5570160429
(1979)Doi:10.1021/jo01156a018
(1949)
