1041024-78-5Relevant academic research and scientific papers
Enantio- and diastereoselective catalytic alkylation reactions with aziridines
Moss, Thomas A.,Fenwick, David R.,Dixon, Darren J.
, p. 10076 - 10077 (2008)
The first asymmetric phase transfer catalyzed alkylation reaction of a range of carbon acids with N-sulfonyl aziridines is reported. When 10 mol % of a cinchona derived quaternary ammonium salt was employed as the catalyst under mildly basic conditions, N
Organocatalytic Michael addition of indanone carboxylates to vinyl selenone for the asymmetric synthesis of polycyclic pyrrolidines
Sternativo, Silvia,Walczak, Ola,Battistelli, Benedetta,Testaferri, Lorenzo,Marini, Francesca
, p. 10536 - 10541,6 (2012/12/12)
A Michael addition of racemic indanone carboxylates to vinyl selenone catalyzed by C6′hydroxyl cinchona derivatives is the key step of a synthetic sequence for a practical access to highly enantioenriched (up to 98% ee) polycyclic pyrrolidines bearing contiguous tertiary and quaternary stereocenters.
Organocatalytic Michael addition of indanone carboxylates to vinyl selenone for the asymmetric synthesis of polycyclic pyrrolidines
Sternativo, Silvia,Walczak, Ola,Battistelli, Benedetta,Testaferri, Lorenzo,Marini, Francesca
, p. 10536 - 10541 (2013/01/15)
A Michael addition of racemic indanone carboxylates to vinyl selenone catalyzed by C6′hydroxyl cinchona derivatives is the key step of a synthetic sequence for a practical access to highly enantioenriched (up to 98% ee) polycyclic pyrrolidines bearing contiguous tertiary and quaternary stereocenters.
