A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Highly Enantioselective Kinetic Resolution of Michael Adducts through N-Heterocyclic Carbene Catalysis: An Efficient Asymmetric Route to Cyclohexenes
Tekijät: Chen XY, Li S, Liu Q, Kumar M, Peuronen A, Rissanen K, Enders D
Kustantaja: WILEY-V C H VERLAG GMBH
Julkaisuvuosi: 2018
Lehti:Chemistry - A European Journal
Tietokannassa oleva lehden nimiCHEMISTRY-A EUROPEAN JOURNAL
Lehden akronyymi: CHEM-EUR J
Vuosikerta: 24
Numero: 39
Aloitussivu: 9735
Lopetussivu: 9738
Sivujen määrä: 4
ISSN: 0947-6539
eISSN: 1521-3765
DOI: https://doi.org/10.1002/chem.201802420
Tiivistelmä
A highly efficient strategy for the kinetic resolution of Michael adducts was realized using a chiral N-heterocyclic carbene catalyst. The kinetic resolution provides a new convenient route to single diastereomers of cyclohexenes and Michael adducts in good yields with high enantiomeric excesses (up to 99% ee with a selectivity factor of up to 458). This "two flies with one swat" concept allows the synthesis of these two synthetically valuable compound classes at the same time by a single transformation.
A highly efficient strategy for the kinetic resolution of Michael adducts was realized using a chiral N-heterocyclic carbene catalyst. The kinetic resolution provides a new convenient route to single diastereomers of cyclohexenes and Michael adducts in good yields with high enantiomeric excesses (up to 99% ee with a selectivity factor of up to 458). This "two flies with one swat" concept allows the synthesis of these two synthetically valuable compound classes at the same time by a single transformation.
Turun yliopiston Tutkimustietojärjestelmän portaali