Abstract
Synthesis of 5-carbomethoxy-3-formyl-5,6-dihydroindolo-[2,3-a]indolizines (10 and 12) and 6-carbomethoxy-3-hydroxy-6,7-dihydroindolo[2,3-a]quinolizinium sulphates (11 and 13) have been achieved. Interestingly, the compound (5R)-(-)-5-carbomethoxy-3-formyl-5,6-dihydroindolo[2,3-a]indolizine (10) intercalated mannose-grafted microspheres was found to be an effective drug, whereas its optical antipode 12 showed no activity at all, against parasite, Leishmania donovani strain AG83 in hamsters model both in-vitro and in-vivo.
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Jaisankar, P., Pal, B., Manna, R. K., Pradhan, P. K., Medda, S., Basu, M. K., & Giri, V. S. (2003). Synthesis of antileishmanial (5R)-(-)-5-Carbomethoxy-3-formyl-5,6- dihydroindolo-[2,3-a]-indolizine. Arkivoc, 2003(9), 150–157. https://doi.org/10.3998/ark.5550190.0004.918
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