1245730-40-8Relevant articles and documents
Ruthenium lewis acid catalyzed asymmetric 1,3-dipolar cycloadditions between N -methylnitrones and enals
Badoiu, Andrei,Bernardinelli, Gerald,Kuendig, E. Peter
, p. 2207 - 2212 (2010)
N-Methylisoxazolidines are formed in good yields and high regio-, diastereo- and enantioselectivity via asymmetric 1,3-dipolar cycloaddition of nitrones with enals catalyzed by a chiral ruthenium Lewis acid. Electronic effects in the dipole are the key to activation of these substrates for efficient catalysis. Georg Thieme Verlag Stuttgart - New York.