Construction of Bicyclo[3.2.1]octanes with Four Stereogenic Centers by Organocatalytic Domino Michael/Aldol Reaction

Autor: Ludovic Gremaud, Alice Lefranc, Alexandre Alexakis
Jazyk: angličtina
Rok vydání: 2014
Předmět:
Zdroj: Organic Letters, Vol. 16, No 20 (2014) pp. 5242-5245
ISSN: 1523-7060
Popis: An enantio- and diastereoselective organocatalytic domino Michael/Aldol reaction for the direct preparation of synthetically and medicinally relevant bicyclo[3.2.1]octane derivatives with four stereogenic centers, including two quaternary carbons, has been described. The reaction tolerates a large variety of substituents on β,γ-unsaturated 1,2-ketoesters and cyclic 1,3-ketoesters. It allows for the formation of various bicyclo[3.2.1]octanes in good yields (53-98%), diastereoselectivities (1:1 to 5:1 dr), and enantioselectivities (up to 95:5 ee).
Databáze: OpenAIRE