Effects of the preparation method on the performance of the Cu/ZnO/Al2O3 catalyst for the manufacture of l-phenylalaninol with high ee selectivity from l-phenylalanine methyl ester

2014 ◽  
Vol 4 (4) ◽  
pp. 1132-1143 ◽  
Author(s):  
Zhangping Shi ◽  
Xiuzhen Xiao ◽  
Dongsen Mao ◽  
Guanzhong Lu
Keyword(s):  
Methyl Ester ◽  
Catalytic Hydrogenation ◽  
Preparation Method ◽  
Phenylalanine Methyl Ester ◽  
Al2o3 Catalyst

Efficient catalytic hydrogenation of l-phenylalanine methyl ester to l-phenylalaninol over the Cu/ZnO/Al2O3 catalyst with ~100% ee selectivity.

scholarly journals A highly effective and stable CuZn0.3MgxAlOycatalyst for the manufacture of chirall-phenylalaninol: the role of Mg and its hydrotalcite-like precursor

2016 ◽  
Vol 6 (10) ◽  
pp. 3457-3467 ◽  
Author(s):  
Zhangping Shi ◽  
Shuangshuang Zhang ◽  
Xiuzhen Xiao ◽  
Dongsen Mao ◽  
Guanzhong Lu
Keyword(s):  
Methyl Ester ◽  
Catalytic Hydrogenation ◽  
Highly Effective ◽  
Phenylalanine Methyl Ester

A highly effective and stable CuZn0.3Mg0.1AlOycatalyst derived from a Cu-rich hydrotalcite-like precursor was prepared for the catalytic hydrogenation ofl-phenylalanine methyl ester tol-phenylalaninol with ~100% ee selectivity.

scholarly journals 4-fluorobenzylamine and phenylalanine methyl ester conjugates OF 2-nitroimidazole: Evaluation as hypoxic cell radiosensitizers

1992 ◽  
Vol 22 (3) ◽  
pp. 593-596 ◽  
Author(s):  
Pradeep K. Arg ◽  
Sudha Garg ◽  
William G. Degraff ◽  
Michael R. Zalutsky ◽  
James B. Mitchell
Keyword(s):  
Methyl Ester ◽  
Hypoxic Cell ◽  
Phenylalanine Methyl Ester

Synthesis of aspartame via asymmetric hydrogenation of N-protected (Z)-N-.alpha.-L-aspartyl-.DELTA.-phenylalanine methyl ester

1986 ◽  
Vol 51 (7) ◽  
pp. 1126-1128 ◽  
Author(s):  
Claudio Fuganti ◽  
Piero Grasselli ◽  
Luciana Malpezzi ◽  
Paolo Casati
Keyword(s):  
Methyl Ester ◽  
Asymmetric Hydrogenation ◽  
Phenylalanine Methyl Ester

scholarly journals Catalytic hydrogenation of straight vegetable oil using NiMo/ Al2O3 catalyst for biodiesel production

2018 ◽  
Vol 67 ◽  
pp. 02045
Author(s):  
SD Sumbogo Murti ◽  
J. Prasetyo ◽  
G.W. Murti ◽  
Z. D. Hastuti ◽  
F. M. Yanti
Keyword(s):  
Vegetable Oil ◽  
Catalytic Hydrogenation ◽  
Cooling System ◽  
Cetane Number ◽  
Chemical Properties ◽  
Raw Material ◽  
Biodiesel Production ◽  
Operation Condition ◽  
Straight Vegetable Oil ◽  
Al2o3 Catalyst

The attractiveness of biodiesel as an alternative fuel compared to fossil fuels because it has many advantages such as the availability of abundant raw materials, more environmentally friendly, high combustion efficiency, low sulphur content, high cetane number and biodegradability. Making biodiesel from straight vegetable oil (VGO) has been done through the catalytic hydrogenation process. A VGO of callophylum inophyllum oil was treated via degumming and neutralisation to remove all impurities before hydroprocessing. Hydroprocessing was carried out in a 500ml autoclave at 30 – 50 MPa of initial hydrogen pressure, 300 – 400oC of reaction temperature and equipped with stirrer and cooling system. NiMo/Al2O3 catalyst was activated with CS2 mixture at 370oC prior to the reaction. Some physical and chemical properties of the catalytic hydroprocessing product have been investigated in accordance to ASTM standard. The measurement result of product varies according to the operation condition. The result showed that callophyllum inophyllum oil can be used as raw material for biodiesel production over NiMo/Al2O3. Sulfided NiMo/Al2O3 catalysts are preferred due to high diesel yield.

Crystal-to-Crystal Diastereoselective Transformation of 2,4,6-Triisopropyl-4'-(S)-phenylalaninocarbonylbenzophenone Methyl Ester

1998 ◽  
Vol 54 (6) ◽  
pp. 907-911 ◽  
Author(s):  
H. Hosomi ◽  
Y. Ito ◽  
S. Ohba
Keyword(s):  
Crystal Structure ◽  
High Pressure ◽  
Methyl Ester ◽  
Absolute Configuration ◽  
Crystal Structure Analysis ◽  
X Ray Diffraction ◽  
Pass Filter ◽  
X Ray ◽  
Ultra High Pressure ◽  
Phenylalanine Methyl Ester

Dissymmetry of the photoproduct was induced by using a chiral substituent, (S)-methylphenylalanine, in the title compound {N-4-(2,4,6-triisopropylbenzoyl)benzoyl]-(S)-phenylalanine methyl ester (I)}. On irradiation with light from a 250 W ultra-high-pressure Hg lamp for 7 h through a long-pass filter, the photoreaction in a crystal was 100% complete without the loss of crystallinity. The crystal structures (I), before, and (II) {N-[4-(7-hydroxy-3,5-diisopropyl-8,8-dimethylbicyclo[4.2.0]octa-1,3,5-trien-7-yl)benzoyl]-(S)-phenylalanine methyl ester}, after photocyclization, have been determined by X-ray diffraction. For comparison, a crystal structure analysis has also been carried out for the photoproduct (III) of the 3′-COOMe derivative after recrystallization {methyl 3-(7-hydroxy-3,5-diisopropyl-8,8-dimethylbicyclo[4.2.0]octa-1,3,5-trien-7-yl)benzoate}. The dihedral angle between the central carbonyl plane and the triisopropylphenyl ring deviates from 90° by 10 (1)° in (I), which makes an imbalance in the intramolecular O(carbonyl)...H(methine) distances of the isopropyl groups at positions 2 and 6. The crystal structure of (II) indicates that the nearer methine H was predominantly abstracted by the carbonyl O atom in the reaction. The absolute configuration around the asymmetric C atom in the cyclobutenol ring of the product is S.

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