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Recent advances in the synthesis of naturally occurring pyrrolidines, pyrrolizidines and indolizidine alkaloids using proline as a unique chiral synthon
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Citations
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References
2013
Year
Enantioselective SynthesisEngineeringBiochemistryUnique Chiral SynthonViable Synthetic PrecursorWide SpectrumOrganic ChemistryNatural ProductsSynthetic ChemistryStereoselective SynthesisPharmacologyRecent AdvancesIndolizidine AlkaloidsBiomolecular EngineeringNatural Product Synthesis
The present article describes the synthesis of a wide spectrum of natural products of the class pyrrolidines, pyrrolizidines and indolizidines using proline as a viable synthetic precursor. The review emphasizes the versatility of the basic unit of proline as a useful chiral synthon confined for the synthesis of only natural products of the above mentioned families. The vast coverage of the synthesis of these natural products is presented for a period from 1990 onwards. The synthesis of all ranges of alkaloids from simple to complex molecules is presented under the groups of alkaloids.
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