Forró Enikő
Forró Enikő
University of Szeged, Institute of Pharmaceutical Chemistry
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Cited by
Cited by
Advanced procedure for the enzymatic ring opening of unsaturated alicyclic β-lactams
E Forró, F Fülöp
Tetrahedron: Asymmetry 15 (18), 2875-2880, 2004
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
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
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
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
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
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
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
Synthesis of orthogonally protected azepane β-amino ester enantiomers
B Kazi, L Kiss, E Forró, F Fülöp
Tetrahedron Letters 51 (1), 82-85, 2010
Synthesis of 4-aryl-substituted β-lactam enantiomers by enzyme-catalyzed kinetic resolution
E Forró, F Fülöp
Tetrahedron: Asymmetry 12 (16), 2351-2358, 2001
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
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
Enzymatic resolution of alicyclic β-lactams
J Kámán, E Forró, F Fülöp
Tetrahedron: Asymmetry 11 (7), 1593-1600, 2000
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
Synthesis of novel isoxazoline-fused cispentacin stereoisomers
L Kiss, M Nonn, E Forró, R Sillanpää, F Fülöp
Tetrahedron Letters 50 (21), 2605-2608, 2009
An efficient enzymatic synthesis of benzocispentacin and its new six‐and seven‐membered homologues
E Forró, F Fülöp
Chemistry–A European Journal 12 (9), 2587-2592, 2006
An efficient new enzymatic method for the preparation of β-aryl-β-amino acid enantiomers
G Tasnádi, E Forró, F Fülöp
Tetrahedron: Asymmetry 19 (17), 2072-2077, 2008
A new strategy for the preparation of heterocyclic β-amino esters: orthogonally protected β-amino esters with a piperidine skeleton
L Kiss, B Kazi, E Forró, F Fülöp
Tetrahedron Letters 49 (2), 339-342, 2008
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
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
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