1369963-65-4Relevant academic research and scientific papers
Domino elimination/nucleophilic addition in the synthesis of chiral pyrrolidines
Flores, Marife,Garcia-Garcia, Pilar,Garrido, Narciso M.,Marcos, Isidro S.,Sanz-Gonzalez, Francisca,Diez, David
, p. 7068 - 7075 (2013/08/15)
Polyhydroxylated pyrrolidines have been synthesized in a one-pot procedure by the addition of an organometallic reagent to isoxazolidines obtained by a 1,3-dipolar cycloaddition between nitrones and vinylsulfones. This method highlights sulfone reactivity and provides an easy approach for the preparation of chiral pyrrolidines using cyclic imines as key intermediates.
1,3-Dipolar cycloaddition of nitrones with phenylvinyl sulfone. An experimental and theoretical study
Flores, Marife,Garcia, Pilar,Garrido, Narciso M.,Nieto, Carlos T.,Basabe, Pilar,Marcos, Isidro S.,Sanz-Gonzalez, Francisca,Goodman, Jonathan M.,Diez, David
experimental part, p. 76 - 85 (2012/05/20)
The addition of three nitrones to phenylvinylsulfone, 1, has been studied. The stereochemistry previously established by two-dimensional NMR techniques was confirmed by X-ray crystal structure determination. Theoretical studies made us propose that this r
