RT Journal Article
T1 Catalytic Enantioselective Cyclopropylalkynylation of Aldimines Generated In Situ from α-Amido Sulfones
A1 Monleón Ventura, Alicia
A1 Blay Llinares, Gonzalo
A1 Pedro, José Ramón
K1 Catàlisi
K1 Química orgànica
AB 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.
YR 2022
FD 2022
LK https://hdl.handle.net/10550/83111
UL https://hdl.handle.net/10550/83111
LA eng
NO 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
DS RODERIC
RD 17 jul 2026