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Forró Enikő
Forró Enikő
University of Szeged, Institute of Pharmaceutical Chemistry
Verified email at pharm.u-szeged.hu - Homepage
Title
Cited by
Cited by
Year
Advanced procedure for the enzymatic ring opening of unsaturated alicyclic β-lactams
E Forró, F Fülöp
Tetrahedron: Asymmetry 15 (18), 2875-2880, 2004
862004
Comparison of the separation efficiencies of Chirobiotic T and TAG columns in the separation of unusual amino acids
A Péter, A Árki, D Tourwé, E Forró, F Fülöp, DW Armstrong
Journal of Chromatography A 1031 (1-2), 159-170, 2004
732004
High-performance liquid chromatographic enantioseparation of β-amino acid stereoisomers on a (+)-(18-crown-6)-2, 3, 11, 12-tetracarboxylic acid-based chiral stationary phase
R Berkecz, A Sztojkov-Ivanov, I Ilisz, E Forró, F Fülöp, MH Hyun, A Péter
Journal of Chromatography A 1125 (1), 138-143, 2006
672006
A new route to enantiopure β‐aryl‐substituted β‐amino acids and 4‐aryl‐substituted β‐lactams through lipase‐catalyzed enantioselective ring cleavage of β‐lactams
E Forró, T Paál, G Tasnádi, F Fülöp
Advanced Synthesis & Catalysis 348 (7‐8), 917-923, 2006
672006
Preparation of (1R, 8S)-and (1S, 8R)-9-azabicyclo [6.2. 0] dec-4-en-10-one: Potential starting compounds for the synthesis of anatoxin-a
E Forró, J Árva, F Fülöp
Tetrahedron: Asymmetry 12 (4), 643-649, 2001
642001
Synthesis of enantiopure 1, 4-ethyl-and 1, 4-ethylene-bridged cispentacin by lipase-catalyzed enantioselective ring opening of β-lactams
E Forró, F Fülöp
Tetrahedron: Asymmetry 15 (4), 573-575, 2004
632004
Molecular Basis for the Enantioselective Ring Opening of β‐Lactams Catalyzed by Candida antarctica Lipase B
S Park, E Forró, H Grewal, F Fülöp, RJ Kazlauskas
Advanced Synthesis & Catalysis 345 (8), 986-995, 2003
632003
Synthesis of orthogonally protected azepane β-amino ester enantiomers
B Kazi, L Kiss, E Forró, F Fülöp
Tetrahedron Letters 51 (1), 82-85, 2010
562010
Stereoselective synthesis of hydroxylated β-aminocyclohexanecarboxylic acids
L Kiss, E Forró, TA Martinek, G Bernáth, N De Kimpe, F Fülöp
Tetrahedron 64 (22), 5036-5043, 2008
562008
Synthesis of 4-aryl-substituted β-lactam enantiomers by enzyme-catalyzed kinetic resolution
E Forró, F Fülöp
Tetrahedron: Asymmetry 12 (16), 2351-2358, 2001
532001
Recent lipase-catalyzed hydrolytic approaches to pharmacologically important β-and γ-amino acids
E Forró, F Fulop
Current medicinal chemistry 19 (36), 6178-6187, 2012
512012
Total synthesis of crispine A enantiomers through a Burkholderia cepacia lipase-catalysed kinetic resolution
E Forró, L Schönstein, F Fülöp
Tetrahedron: Asymmetry 22 (11), 1255-1260, 2011
512011
Enzymatic resolution of alicyclic β-lactams
J Kámán, E Forró, F Fülöp
Tetrahedron: Asymmetry 11 (7), 1593-1600, 2000
512000
Lipase-catalyzed kinetic and dynamic kinetic resolution of 1, 2, 3, 4-tetrahydroisoquinoline-1-carboxylic acid
TA Paál, E Forró, A Liljeblad, LT Kanerva, F Fülöp
Tetrahedron: asymmetry 18 (12), 1428-1433, 2007
502007
Synthesis of novel isoxazoline-fused cyclic β-amino esters by regio-and stereo-selective 1, 3-dipolar cycloaddition
M Nonn, L Kiss, E Forró, Z Mucsi, F Fülöp
Tetrahedron 67 (22), 4079-4085, 2011
492011
Regio-and diastereoselective fluorination of alicyclic β-amino acids
L Kiss, E Forró, S Fustero, F Fülöp
Organic & Biomolecular Chemistry 9 (19), 6528-6534, 2011
492011
Synthesis of novel isoxazoline-fused cispentacin stereoisomers
L Kiss, M Nonn, E Forró, R Sillanpää, F Fülöp
Tetrahedron Letters 50 (21), 2605-2608, 2009
482009
New gas chromatographic method for the enantioseparation of β-amino acids by a rapid double derivatization technique
E Forró
Journal of Chromatography A 1216 (6), 1025-1029, 2009
472009
Vapour-assisted enzymatic hydrolysis of β-lactams in a solvent-free system
E Forró, F Fülöp
Tetrahedron: Asymmetry 19 (8), 1005-1009, 2008
472008
Synthesis and Conformational Study of 1,3,2-Oxazaphosphorino[4,3-a]isoquinolines:  A New Ring System
T Martinek, E Forró, G Günther, R Sillanpää, F Fülöp
The Journal of organic chemistry 65 (2), 316-321, 2000
472000
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