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An Oxazoline-Mediated Synthesis of the Pyrrolophenanthridine Alkaloids and Some Novel Derivatives
55
Citations
55
References
1996
Year
N-benzyl-7-bromoindoline 25HeterocyclicIntermediate BiarylBiochemistryOxazoline-mediated SynthesisMedicineOrganic ChemistryPyrrolophenanthridine AlkaloidsSynthetic ChemistryUnsymmetrical BiarylHeterocycle ChemistryPharmacologyNovel DerivativesDrug DiscoveryNatural Product Synthesis
An unsymmetrical biaryl coupling between the Grignard of N-benzyl-7-bromoindoline 25 and the appropriately substituted (o-methoxyaryl)oxazoline 15 leads to an intermediate biaryl which can be elaborated in one step to the 1H-pyrrolo[3,2,1-de]phenanthridine ring system. This simple two-step sequence provides general access to the pyrrolophenanthridine alkaloids 2−6.
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