Homogeneous RuCl 2 (PPh 3 ) 3 -catalyzed regioselective liquid-phase transfer hydrogenation of carbon-carbon double bond in chlorobenzylidene ketones with ethylene glycol as hydrogen donor

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Standard

Homogeneous RuCl 2 (PPh 3 ) 3 -catalyzed regioselective liquid-phase transfer hydrogenation of carbon-carbon double bond in chlorobenzylidene ketones with ethylene glycol as hydrogen donor. / Mukhopadhyay, Sudip; Yaghmur, Anan; Benichou, Axel; Sasson, Yoel.

I: Organic Process Research and Development, Bind 4, Nr. 6, 01.11.2000, s. 571-574.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Mukhopadhyay, S, Yaghmur, A, Benichou, A & Sasson, Y 2000, 'Homogeneous RuCl 2 (PPh 3 ) 3 -catalyzed regioselective liquid-phase transfer hydrogenation of carbon-carbon double bond in chlorobenzylidene ketones with ethylene glycol as hydrogen donor', Organic Process Research and Development, bind 4, nr. 6, s. 571-574.

APA

Mukhopadhyay, S., Yaghmur, A., Benichou, A., & Sasson, Y. (2000). Homogeneous RuCl 2 (PPh 3 ) 3 -catalyzed regioselective liquid-phase transfer hydrogenation of carbon-carbon double bond in chlorobenzylidene ketones with ethylene glycol as hydrogen donor. Organic Process Research and Development, 4(6), 571-574.

Vancouver

Mukhopadhyay S, Yaghmur A, Benichou A, Sasson Y. Homogeneous RuCl 2 (PPh 3 ) 3 -catalyzed regioselective liquid-phase transfer hydrogenation of carbon-carbon double bond in chlorobenzylidene ketones with ethylene glycol as hydrogen donor. Organic Process Research and Development. 2000 nov. 1;4(6):571-574.

Author

Mukhopadhyay, Sudip ; Yaghmur, Anan ; Benichou, Axel ; Sasson, Yoel. / Homogeneous RuCl 2 (PPh 3 ) 3 -catalyzed regioselective liquid-phase transfer hydrogenation of carbon-carbon double bond in chlorobenzylidene ketones with ethylene glycol as hydrogen donor. I: Organic Process Research and Development. 2000 ; Bind 4, Nr. 6. s. 571-574.

Bibtex

@article{75006febe8314a06bd74261901226f0d,
title = "Homogeneous RuCl 2 (PPh 3 ) 3 -catalyzed regioselective liquid-phase transfer hydrogenation of carbon-carbon double bond in chlorobenzylidene ketones with ethylene glycol as hydrogen donor",
abstract = "The regioselective transfer hydrogenation of a carbon-carbon double bond of different chlorobenzylidene ketones is effectuated in ethylene glycol with a very high selectivity in the presence of homogeneous, tris(triphenylphosphine)ruthenium-(II) chloride catalyst. Different important process parameters such as temperature, catalyst loading, and reaction period are studied. The reaction follows a first-order kinetics, and the energy of activation was found to be 52 kJ/mol.",
author = "Sudip Mukhopadhyay and Anan Yaghmur and Axel Benichou and Yoel Sasson",
year = "2000",
month = nov,
day = "1",
language = "English",
volume = "4",
pages = "571--574",
journal = "Organic Process Research and Development",
issn = "1083-6160",
publisher = "American Chemical Society",
number = "6",

}

RIS

TY - JOUR

T1 - Homogeneous RuCl 2 (PPh 3 ) 3 -catalyzed regioselective liquid-phase transfer hydrogenation of carbon-carbon double bond in chlorobenzylidene ketones with ethylene glycol as hydrogen donor

AU - Mukhopadhyay, Sudip

AU - Yaghmur, Anan

AU - Benichou, Axel

AU - Sasson, Yoel

PY - 2000/11/1

Y1 - 2000/11/1

N2 - The regioselective transfer hydrogenation of a carbon-carbon double bond of different chlorobenzylidene ketones is effectuated in ethylene glycol with a very high selectivity in the presence of homogeneous, tris(triphenylphosphine)ruthenium-(II) chloride catalyst. Different important process parameters such as temperature, catalyst loading, and reaction period are studied. The reaction follows a first-order kinetics, and the energy of activation was found to be 52 kJ/mol.

AB - The regioselective transfer hydrogenation of a carbon-carbon double bond of different chlorobenzylidene ketones is effectuated in ethylene glycol with a very high selectivity in the presence of homogeneous, tris(triphenylphosphine)ruthenium-(II) chloride catalyst. Different important process parameters such as temperature, catalyst loading, and reaction period are studied. The reaction follows a first-order kinetics, and the energy of activation was found to be 52 kJ/mol.

UR - http://www.scopus.com/inward/record.url?scp=0034345920&partnerID=8YFLogxK

M3 - Journal article

AN - SCOPUS:0034345920

VL - 4

SP - 571

EP - 574

JO - Organic Process Research and Development

JF - Organic Process Research and Development

SN - 1083-6160

IS - 6

ER -

ID: 221830117