Grupo de síntesis química y catálisis - GIC 21/041
Stony Brook University
Stony Brook, Estados UnidosPublikationen in Zusammenarbeit mit Forschern von Stony Brook University (7)
2014
-
Inexpensive chemical method for preparation of enantiomerically pure phenylalanine
Amino Acids, Vol. 46, Núm. 4, pp. 945-952
-
Synthesis and stereochemical assignments of diastereomeric Ni(II) complexes of glycine Schiff base with (R)-2-(N-{2-[N-alkyl-N-(1-phenylethyl)-amino] acetyl}amino)benzophenone; A case of configurationally stable stereogenic nitrogen
Beilstein Journal of Organic Chemistry, Vol. 10, pp. 442-448
2011
-
Asymmetric synthesis of sterically and electronically demanding linear ω-trifluoromethyl containing amino acids via alkylation of chiral equivalents of nucleophilic glycine and alanine
Journal of Organic Chemistry, Vol. 76, Núm. 2, pp. 684-687
-
Biomimetic transamination - a metal-free alternative to the reductive amination. Application for generalized preparation of fluorine-containing amines and amino acids
Current Organic Synthesis, Vol. 8, Núm. 2, pp. 281-294
-
Reply to the 'comment on "theoretical investigations into the enantiomeric and racemic forms of α-(trifluoromethyl)lactic acid"' by M. A. Suhm and M. Albrecht, Phys. Chem. Chem. Phys., 2011, 13, DOI: 10.1039/c0cp02455d
Physical Chemistry Chemical Physics, Vol. 13, Núm. 9, pp. 4161-4162
-
Self-Disproportionation of enantiomers via sublimation; new an truly green dimension in optical purification
Current Organic Synthesis, Vol. 8, Núm. 2, pp. 310-317
-
Theoretical investigations into the enantiomeric and racemic forms of α-(trifluoromethyl)lactic acid
Physical Chemistry Chemical Physics, Vol. 13, Núm. 3, pp. 811-817