نتایج جستجو برای: racemic phenylalanine methyl ester

تعداد نتایج: 147397  

2008
Åsmund Kaupang Marianne Bolsønes Thywill Gamadeku Tore Hansen Martin Johanson Hennum Carl Henrik Görbitz

In the racemic hydro-chloride salt of the title ester, C(19)H(22)Cl(2)NO(2) (+)·Cl(-), the penta-noic acid chain shows a mixture of trans and gauche orientations to give an overall helical conformation. The dihedral angle between the two aromatic rings is 26.11 (10)°. The charged secondary amine function participates in two N-H⋯Cl hydrogen bonds.

Journal: :Chemical communications 2012
Mu-Wang Chen Qing-An Chen Ying Duan Zhi-Shi Ye Yong-Gui Zhou

Asymmetric hydrogenolysis of racemic tertiary alcohols, 3-substituted 3-hydroxyisoindolin-1-ones, was developed using chiral phosphoric acid as catalyst and a Hantzsch ester as the hydrogen source with up to 95% ee. The reaction process of this asymmetric transfer hydrogenation may occur directly through the acyliminium ion intermediate.

2011
Victor A. Vasin Irina Yu. Bolusheva Vyacheslav A. Neverov Nikolai V. Somov

The title compound, C(13)H(13)NO(4)S, is a racemic mixture of enanti-omers. Short intra-molecular contacts between sulfonyl O and ester carbonyl C atoms are observed [C⋯O = 2.881 (1), 2.882 (1) and 2.686 (1) Å], indicating the possibility of donor-acceptor inter-actions between these groups. The dihedral angle between the phenyl and cyclopropyl rings is 79.3 (1)°.

Journal: :The Journal of biological chemistry 1988
F P Guengerich L A Peterson R H Böcker

Cytochrome P-450 (P-450)-catalyzed oxidation of 2,6-dimethyl-4-phenyl-3,5-pyridinedicarboxylic acid diethyl ester gives rise to 2,6-dimethyl-4-phenyl-3,5-pyridinedicarboxylic acid monoethyl ester and to 2-hydroxymethyl-6-methyl-4-phenyl-3,5-pyridinedicarboxylic acid diethyl ester, identified in this work. A pyridine hydroxymethyl diester of the sort of the latter compound is novel; under acidic...

Journal: :The Journal of biological chemistry 1952
D S ROBINSON J P GREENSTEIN

Hydroxy-L-proline was first isolated by Fischer in 1902 from a hydrolysate of gelatin (l).l The synthesis and determination of the structure were reported by Leuchs and coworkers (5--g), and, in 1919, the separation of the two racemic stereoisomers and the resolution of each racemate through mixtures of quinine with the corresponding N-phenylisocyanate derivatives were accomplished (5). In the ...

Two modified methods for assaying sodium diclofenac were developed by GC and HPLC. Diclofenac was converted into methyl ester derivative by methyl iodide in acetone. The ester was extract and subjected to GLC with flame ionization detector. %5 SE-30/chrom W-HP (80-100 mesh) was used as a column in GC. For reversed phase HPLC, the mobile phase was methanol and water (55-45). The separation was p...

Journal: :Journal of medicinal chemistry 2002
Sybille Wittich Hans Scherf Changping Xie Gerald Brosch Peter Loidl Clarissa Gerhäuser Manfred Jung

Inhibitors of histone deacetylases (HDACs) are a new class of anticancer agents that affect gene regulation. We had previously reported the first simple synthetic HDAC inhibitors with in vitro activity at submicromolar concentrations. Here, we present structure-activity data on modifications of a phenylalanine-containing lead compound including amino acid amides as well as variations of the ami...

2017
Chiung-Yao Huang Jui-Hsin Su Chih-Chuang Liaw Ping-Jyun Sung Pei-Lun Chiang Tsong-Long Hwang Chang-Feng Dai Jyh-Horng Sheu

A continuing chemical investigation of the ethyl acetate (EtOAc) extract of a reef soft coral Sinularia brassica, which was cultured in a tank, afforded four new steroids with methyl ester groups, sinubrasones A-D (1-4) for the first time. In particular, 1 possesses a β-D-xylopyranose. The structures of the new compounds were elucidated on the basis of spectroscopic analyses. The cytotoxicities...

Journal: :The Journal of biological chemistry 1948
J E SNOKE G W SCHWERT H NEURATH

It was recently found that the proteolytic enzymes trypsin (19 and chymotrypsin (2) possess specific esterase activity. In addition to catalyzing the hydrolysis of specific peptides (3-7), these enzymes also catalyze the hydrolysis of those esters which possess the structural environment of the specific peptides. In order to substantiate further the suggestion of Schwert et al. (1) that the spe...

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