Publication | Closed Access
Telescoped Synthesis of Stereodefined Pyrrolidines
55
Citations
32
References
2013
Year
High EnantioselectivityAvailable TetramisoleTelescoped SynthesisLewis BaseOrganic ChemistryStereoselective SynthesisChemistryHeterocycle ChemistryPharmacologySynthetic ChemistryEnantioselective Synthesis
Telescoped and one-pot olefination/asymmetric functionalization approaches to disubstituted pyrrolidines (dr up to 99:1, up to 99% ee) have been developed using commercially available tetramisole (0.1 to 5 mol %). Using OTMS-quinidine as the Lewis base gives preferential access to an anti-configured pyrrolidine in high enantioselectivity.
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