Uk. Bandarage et al., Total syntheses of racemic albifloranine and its anti-addictive congeners,including 18-methoxycoronaridine, TETRAHEDRON, 55(31), 1999, pp. 9405-9424
Condensation of methyl 3-benzyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole-5
-carboxylate (12) with 4-(1,3-dioxolan-2-yl)-6-benzylaxyhexanal (11a) provi
ded the tetracyclic intermediates methyl (3aSR,4RS,11bRS)-3-benzyl-2,3,3a,4
,5,7-hexahydro-4-[2-zeta-(1,3-dioxalan-2-yl)-4-benzyloxy)-1-butyl]-1H-pyrro
lo[2,3-d]carbazole-6-carboxylates (14a,15a), which were further elaborated
to afford racemic albifloranine (3). The first total synthesis of albiflora
nine was completed in 13 steps, with an overall 7% yield. Ester and ether d
erivatives of albifloranine were synthesized for evaluation as anti-addicti
ve agents. Among these, 18-methoxycoronaridine (20b) stands out as a nontox
ic agent that significantly reduces demand for morphine, cocaine, nicotine
and alcohol in rats. (C) 1999 Elsevier Science Ltd. All rights reserved.