Enantioselective Hydrolysis of Some 2-Aryloxyalkanoic Acid Methyl Esters and Isosteric Analogues Using a Penicillin G Acylase-Based HPLC Monolithic Silica Column-Reference-Cited by-同舟云学术

Enantioselective Hydrolysis of Some 2-Aryloxyalkanoic Acid Methyl Esters and Isosteric Analogues Using a Penicillin G Acylase-Based HPLC Monolithic Silica Column

Published:2002-12-21 Issue:3 Volume:75 Page:535-542
ISSN:0003-2700
Container-title:Analytical Chemistry
language:en
Short-container-title:Anal. Chem.

Author:

Massolini Gabriella¹,Calleri Enrica¹,Lavecchia Antonio¹,Loiodice Fulvio¹,Lubda Dieter¹,Temporini Caterina¹,Fracchiolla Giuseppe¹,Tortorella Paolo¹,Novellino Ettore¹,Caccialanza Gabriele¹

Affiliation:

1. Dipartimento di Chimica Farmaceutica, Universita' di Pavia, Via Taramelli 12, I-27100 Pavia, Italy, Dipartimento di Chimica Farmaceutica e Tossicologica, Universita' di Napoli “Federico II”, Via Domenico Montesano, 49, I-80131 Napoli, Italy, Dipartimento Farmaco-Chimico, Via Orabona 4, I-70126 Bari, Italy, LSP R&D MDA, Merck KGaA, Frankfurter Str 250, D-64293 Darmstadt, Germany, and Dipartimento di Scienze del Farmaco, Universita' “G.D'Annunzio”, Via dei Vestini, I-66100 Chieti, Italy

Publisher

American Chemical Society (ACS)

Subject

Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ac0204193

Reference39 articles.

1. Penicillin acylase has a single-amino-acid catalytic centre

2. Enantioselective recognition of the phenacetyl moiety in the Pen G acylase catalysed hydrolysis of phenylacetate esters

3. Reactions of protonated diamino acids in the gas phase

4. Pen G acylase catalyzed resolution of phenylacetate esters of secondary alcohols

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