Publication | Closed Access
A Facile and Efficient Synthesis of 3,3-Dimethyl Isopropylidene Proline From (+)-3-Carene
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Citations
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References
2010
Year
Combinatorial ChemistryMedicinal ChemistryEngineeringMultigram ScaleNatural SciencesContinuous StereocentersPractical RouteOrganic ChemistryEfficient SynthesisChemistryStereoselective SynthesisPharmacologySynthetic ChemistryEnantioselective SynthesisBiomolecular EngineeringNatural Product Synthesis
A highly efficient and practical route to 3,4-isopropylidene proline I, starting from (+)-3-carene, was developed. The three continuous stereocenters were constructed using the inherent chirality of the starting natural product 2. The overall yield for the 12-step synthesis is 34%. The optimized sequence leading to 1 has been successfully applied on a multigram scale, thereby establishing the practicality of this route.
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