Catalytic Enantioselective Cyclopropylalkynylation of Aldimines Generated In Situ from α-Amido Sulfones
NAGIOS: RODERIC FUNCIONANDO

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

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

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Monleón Ventura, Alicia; Blay Llinares, Gonzalo Perfil; Pedro, José Ramón
This document is a artículoDate2022
A convenient procedure of synthesis of N-carbamoyl-protected propargylic amines substituted with a cyclopropyl group from alpha-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.

    Monleón Ventura, Alicia Blay Llinares, Gonzalo Pedro, José Ramón 2022 Catalytic Enantioselective Cyclopropylalkynylation of Aldimines Generated In Situ from α-Amido Sulfones Molecules 27 12 3763
https://doi.org/10.3390/molecules27123763

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