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methylphenyl carbinol
Known as:
1-phenylethanol
, alpha-hydroxyethylbenzene
, alpha-methylbenzyl alcohol
National Institutes of Health
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Related topics
Related topics
1 relation
Broader (1)
Benzyl Alcohols
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Synthesis and catalytic activity of Ni°-acid activated montmorillonite nanoparticles
Dipanka Dutta
,
B. J. Borah
,
L. Saikia
,
M. G. Pathak
,
P. Sengupta
,
D. Dutta
2011
Corpus ID: 54176954
Highly Cited
2009
Highly Cited
2009
Kinetic hydrogen/deuterium effects in the direct hydrogenation of ketones catalyzed by a well-defined ruthenium diphosphine diamine complex.
Marco Zimmer-De Iuliis
,
R. Morris
Journal of the American Chemical Society
2009
Corpus ID: 893242
The trans-dihydride complex trans-RuH(2)(NH(2)CMe(2)CMe(2)NH(2))((R)-binap) (1) is an active catalyst for the homogeneous…
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Highly Cited
2008
Highly Cited
2008
Direct observations of the metal-ligand bifunctional addition step in an enantioselective ketone hydrogenation.
R. Hamilton
,
S. Bergens
Journal of the American Chemical Society
2008
Corpus ID: 348694
The catalytic intermediate trans-[Ru((R)-BINAP)(H)2((R,R)-dpen)] (1) reacted on mixing with acetophenone in THF at -80 degrees C…
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Highly Cited
2006
Highly Cited
2006
Steric effects in the uncatalyzed and DMAP-catalyzed acylation of alcohols-quantifying the window of opportunity in kinetic resolution experiments.
C. Fischer
,
Shangjie Xu
,
H. Zipse
Chemistry
2006
Corpus ID: 22752600
The kinetics of the reaction of several alcohols (benzyl alcohol, ethanol, 1-phenylethanol, cyclohexanol, and 1-methyl-1…
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Highly Cited
2005
Highly Cited
2005
A succession of isomers of ruthenium dihydride complexes. Which one is the ketone hydrogenation catalyst?
R. Abbel
,
K. Abdur-Rashid
,
Michael Faatz
,
A. Hadžović
,
A. Lough
,
R. Morris
Journal of the American Chemical Society
2005
Corpus ID: 8157123
Reaction of RuHCl(PPh(3))(2)(diamine) (1a, diamine = (R,R)-1,2-diaminocyclohexane, (R,R)-dach; 1b, diamine = ethylenediamine, en…
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Highly Cited
2004
Highly Cited
2004
Lipase-catalysed kinetic resolution of racemates at temperatures from 40 °C to 160 °C in supercritical CO2
A. Overmeyer
,
S. Schrader-Lippelt
,
V. Kasche
,
G. Brunner
Biotechnology Letters
2004
Corpus ID: 23731054
The reaction rate and selectivity of the enzymatic kinetic resolution of ibuprofen and 1-phenylethanol with supercritical CO2 as…
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Highly Cited
2001
Highly Cited
2001
Novel microbial lipases: catalytic activity in reactions in organic media.
F. Cardenas
,
M. de Castro
,
+4 authors
E. Alvarez
Enzyme and Microbial Technology
2001
Corpus ID: 22314231
Highly Cited
2001
Highly Cited
2001
Creation of an enantioselective hydrolase by engineered substrate-assisted catalysis.
Anders O. Magnusson
,
Karl Hult
,
M. Holmquist
Journal of the American Chemical Society
2001
Corpus ID: 46421991
This thesis describes the use of rational redesign to modify the properties of the enzyme Candida antarctica lipase B. Through…
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1998
1998
Asymmetric Reduction of Acetophenone with Calcium‐Alginate‐Entrapped Baker's Yeast in Organic Solvents
D. Griffin
,
Fangxiao Yang
,
G. Carta
,
J. Gainer
Biotechnology progress (Print)
1998
Corpus ID: 701957
Baker's yeast cells entrapped in alginate beads are shown to catalyze reactions in organic solvents when a cofactor regeneration…
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Highly Cited
1996
Highly Cited
1996
Biotechnological application of Pseudomonas aeruginosa lipase: efficient kinetic resolution of amines and alcohols
K. Jaeger
,
K. Liebeton
,
A. Zonta
,
K. Schimossek
,
M. Reetz
Applied Microbiology and Biotechnology
1996
Corpus ID: 32897763
Abstract Pseudomonas aeruginosa secretes an extracellular lipase (EC 3.1.1.3), which has been isolated from culture media of…
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