784191-96-4Relevant academic research and scientific papers
An efficient diastereoselective route to differentially protected anti-4-amino-1-alken-3-ols
Lombardo, Marco,Mosconi, Elisa,Pasi, Filippo,Petrini, Marino,Trombini, Claudio
, p. 1834 - 1837 (2007)
Zinc-promoted hydroxyallylation of α-amidoalkyl arylsulfones 4 using 3-bromo-propenyl methyl carbonate 5 proceeds smoothly in DMF at room temperature to afford high yields of differentially protected anti-1,2-amino alcohols 6.
Reactivity of chiral α-amidoalkylphenyl sulfones with stabilized carbanions. Stereoselective synthesis of optically active 1-aminopyrrolizidine
Giri, Nicola,Petrini, Marino,Profeta, Roberto
, p. 7303 - 7308 (2007/10/03)
Metal enolates and functionalized allylzinc reagents react with optically active α-amidoalkylphenyl sulfones to give N-carbamoylamino derivatives with variable levels of anti diastereoselectivity. Zinc enolates provide comparable results with respect to l
