6533b860fe1ef96bd12c3a78

RESEARCH PRODUCT

Catalytic Enantioselective Cyclopropylalkynylation of Aldimines Generated In Situ from α-Amido Sulfones

Alicia MonleonGonzalo BlayJosé R. Pedro

subject

Organic ChemistryPharmaceutical ScienceStereoisomerismCatalysisAnalytical ChemistryZinc<i>N</i>-carbamoyl-protected propargylic amines; α-amido sulfones; cyclopropylacetylene; BINOL; zinc complexCatàlisiChemistry (miscellaneous)Drug DiscoveryMolecular MedicineSulfonesAminesPhysical and Theoretical ChemistryQuímica orgànica

description

A convenient procedure of synthesis of N-carbamoyl-protected propargylic amines substituted with a cyclopropyl group from α-amido sulfones and cyclopropylacetylene is described. The reaction is catalyzed by a chiral BINOL-type zinc complex and provides the corresponding products in good yields and enantioselectivities.

10.3390/molecules27123763https://hdl.handle.net/10550/83111