Gas chromatographic enantioseparation of derivatized α-amino acids on chiral stationary phases—Past and present

V Schurig - Journal of Chromatography B, 2011 - Elsevier
The historical development of the enantioseparation of derivatized α-amino acids by high-
resolution capillary gas chromatography on chiral stationary phases derived from α-amino …

Use of derivatized cyclodextrins as chiral selectors for the separation of enantiomers by gas chromatography

V Schurig - Annales Pharmaceutiques Françaises, 2010 - Elsevier
The state-of-the-art of enantioseparations of various chiral compounds on derivatized
cyclodextrins, employed as chiral stationary phases (CSPs) by gas chromatography, is …

A norepinephrine coated magnetic molecularly imprinted polymer for simultaneous multiple chiral recognition

J Chen, RP Liang, XN Wang, JD Qiu - Journal of Chromatography A, 2015 - Elsevier
A newly designed molecularly imprinted polymer (MIP) material was developed and
successfully used as recognition element for enantioselective recognition by microchip …

Recent lipase-catalyzed hydrolytic approaches to pharmacologically important β-and γ-amino acids

E Forró, F Fulop - Current medicinal chemistry, 2012 - ingentaconnect.com
Kinetic and sequential kinetic enzymatic routes for the synthesis of enantiomeric β-and γ-
amino acids through enzymatic ring cleavage of the corresponding lactams in organic …

Synthesis of orthogonally protected azepane β-amino ester enantiomers

B Kazi, L Kiss, E Forró, F Fülöp - Tetrahedron Letters, 2010 - Elsevier
A simple and convenient route is presented for the preparation of regio-and stereoisomers of
novel azepane β-amino esters, starting from bicyclic β-lactam isomers. The synthetic …

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, 2011 - Elsevier
Isoxazoline-fused 2-aminocyclopentanecarboxylate derivatives were regio-and stereo-
selectively synthesized by nitrile oxide 1, 3-dipolar cycloaddition to cis-or trans-ethyl-2 …

[PDF][PDF] A new access route to functionalized cispentacins from norbornene β-amino acids.

L Kiss, M Cherepanova, E Forró, F Fülöp - Chemistry-A European …, 2013 - core.ac.uk
The concept of the synthetic route, represented in the retrosynthetic scheme (Scheme 1),
was the functionalization of the CÀC ring double bond of the di-exo-norbornene βlactam by …

Green Strategies for the Preparation of Enantiomeric 5–8-Membered Carbocyclic β-Amino Acid Derivatives through CALB-Catalyzed Hydrolysis

S Shahmohammadi, T Faragó, M Palkó, E Forró - Molecules, 2022 - mdpi.com
Candida antarctica lipase B-catalyzed hydrolysis of carbocyclic 5–8-membered cis β-amino
esters was carried out in green organic media, under solvent-free and ball-milling …

Enantiomers and their resolution

R Santos, KV Pontes, IBR Nogueira - Encyclopedia, 2022 - mdpi.com
Definition Enantiomers share the same chemical formula but have different chemical
structures, ie, type of isomers. Enantiomers are present in several drugs, perfumes, food …

Burkholderia cepacia lipase is an excellent enzyme for the enantioselective hydrolysis of β-heteroaryl-β-amino esters

G Tasnádi, E Forró, F Fülöp - Tetrahedron: Asymmetry, 2009 - Elsevier
The enantioselective (E> 200) lipase PS-catalysed hydrolysis of β-heteroaryl-β-amino esters
is described. The reactions were performed with H2O (0.5 equiv) in either diisopropyl ether …