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Keyword:'benzyl alcohol'
Showing 1-30 of 963 results for "benzyl alcohol" within Papers
Derek W Barnett et al.
Journal of labelled compounds & radiopharmaceuticals, 56(1), 6-11 (2013-11-29)
Chirally deuterated benzyl chlorides were prepared using novel, general hexachloroacetone/polymer-supported triphenylphosphine treatment of chirally deuterated benzyl alcohols. Doubly labeled protected tyrosine was obtained in 62% yield with 86% de at the α-carbon and 82% de at the β-carbon. Key in
T J Etelälahti et al.
Pharmacology, biochemistry, and behavior, 124, 81-85 (2014-05-30)
The anabolic steroid nandrolone decanoate has been reported to increase voluntary ethanol intake in Wistar rats. In recent experiments we received opposite results, with decreased voluntary ethanol intake in both high drinking AA and low drinking Wistar rats after nandrolone
Contact allergy to benzyl alcohol and isopropyl palmitate, ingredients of topical corticosteroid.
S Lazzarini
Contact dermatitis, 8(5), 349-350 (1982-09-01)
Epidural administration of methylprednisolone acetate preserved with benzyl alcohol.
C C King et al.
The Annals of pharmacotherapy, 28(1), 59-60 (1994-01-01)
Contact allergy to benzyl alcohol and benzyl paraben.
G Würbach et al.
Contact dermatitis, 28(3), 187-188 (1993-03-01)
A Basu et al.
Applied microbiology and biotechnology, 62(5-6), 579-585 (2003-04-11)
Pseudomonas putida CSV86 metabolizes 1- and 2-methylnaphthalene through distinct catabolic and detoxification pathways. In spite of the similarity in the steps involved in the methylnaphthalene detoxification and the toluene side-chain hydroxylation pathways, the strain failed to utilize toluene or xylenes.
Influence of vehicles on penetration through human epidermis of benzyl alcohol, isoeugenol and methyl isoeugenol.
Y Jimbo et al.
The Journal of dermatology, 10(3), 241-250 (1983-06-01)
G N Menon et al.
Journal of pharmaceutical sciences, 70(6), 697-698 (1981-06-01)
A stability-indicating, high-performance liquid chromatographic method was developed for the simultaneous determination of hydroxyzine hydrochloride and benzyl alcohol in injection solutions. Separation was achieved using a mu Bondapak C18 column and the eluent [60% water, 25% acetonitrile, and 15% methanol
M Testa et al.
Journal of ocular pharmacology, 3(3), 211-225 (1987-01-01)
Substances derived from biotransformation of non-steroid antiinflammatory drugs (NSAID) produced by patients responsive to the biological liquid oxidant activity (BLOA) test, have been shown to have anticataract activity. They are all aromatic alcohols with physico-chemical properties similar to benzyl alcohols
M LeBel et al.
Developmental pharmacology and therapeutics, 11(6), 347-356 (1988-01-01)
Reports on fatal benzyl alcohol poisoning in premature neonates implied that the toxicity may be due to larger doses per kilogram than for adults. It has been postulated that the load of benzoic acid (metabolite of benzyl alcohol) may exceed
Hassan A Kalviri et al.
Chemical communications (Cambridge, England), (34)(34), 5171-5173 (2010-05-08)
Dibenzyl ethers and benzyl chloride can be obtained in moderate to excellent yields through Pd-catalysed reactions in hydrophobic ionic liquids using microwave or conventional heating.
T P Binder et al.
Molecular pharmacology, 33(4), 477-479 (1988-04-01)
Aryl sulfotransferase (AST) IV catalyzes the 3'-phosphoadenosine 5'-phosphosulfate-dependent sulfation of a variety of benzylic alcohols. Several molecular characteristics of benzylic alcohols were investigated for their ability to influence the catalytic efficiency of a homogeneous preparation of rat hepatic AST IV.
A Dasgupta et al.
Journal of forensic sciences, 42(4), 697-700 (1997-07-01)
Benzyl alcohol is commonly used as an antibacterial agent in a variety of pharmaceutical formulations. Several fatalities in neonates have been linked to benzyl alcohol poisoning. Most methods for measuring benzyl alcohol concentrations in serum utilize direct extraction followed by
Hidemasa Hikawa et al.
Organic & biomolecular chemistry, 10(15), 2942-2945 (2012-03-10)
Palladium-catalyzed S-benzylation of unprotected mercaptobenzoic acids with benzyl alcohols gave only S-benzylated mercaptobenzoic acids in good yields. Water may play an important role for the smooth generation of the (η(3)-benzyl)palladium species by activation of the hydroxyl group of the benzyl
Sjoerd A Veldhuis et al.
Inorganic chemistry, 53(24), 13188-13196 (2014-11-26)
Nanocrystalline barium titanate (8-10 nm crystallite size) was prepared at temperatures of 23-78 °C through reaction of a modified titanium alkoxide precursor in benzyl alcohol with barium hydroxide octahydrate. The room temperature formation of a perovskite phase from solution is
Inna Guterman et al.
Plant molecular biology, 60(4), 555-563 (2006-03-10)
Esters are important contributors to the aroma of numerous flowers and fruits. Acetate esters such as geranyl acetate, phenylethyl acetate and benzyl acetate are generated as a result of the action of alcohol acetyltransferases (AATs). Numerous homologous AATs from various
J Scognamiglio et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50 Suppl 2, S140-S160 (2011-11-01)
A toxicologic and dermatologic review of benzyl alcohol when used as a fragrance ingredient is presented. Benzyl alcohol is a member of the fragrance structural group Aryl Alkyl Alcohols and is a primary alcohol. The AAAs are a structurally diverse
Hidemasa Hikawa et al.
The Journal of organic chemistry, 78(23), 12128-12135 (2013-11-22)
A novel and efficient method for the Au(III)/TPPMS-catalyzed direct substitution reaction of benzhydryl and benzylic alcohols with indoles in water is developed. Au(III)/TPPMS is an effective catalyst for the benzylation of the strong π nucleophile 1-methylindole, while common Brønsted or
José Antonio Morales-Serna et al.
Molecules (Basel, Switzerland), 15(11), 8156-8168 (2010-11-13)
Linear oligomerization of 3,5-dimethyl benzyl alcohol is induced by a montmorillonite clay (Tonsil Optimum Extra), producing 1,3,5,7-tetramethyl-9,10-dihydro-anthracene, which, by loss of protons results in the product 1,3,5,7-tetramethylanthracene. It was also found that the compounds 4-(3´,5´-dimethylbenzyl)-1,3,5,7-tetramethyl-9,10-dihydroanthracece and 4-(3´,5´-dimethylbenzyl)-1,3,5,7-tetra-methylanthracene were formed from
José A Rodríguez-Martínez et al.
The Journal of pharmacy and pharmacology, 63(6), 800-805 (2011-05-19)
Addition of the antimicrobial preservative benzyl alcohol to reconstitution buffer promotes the formation of undesirable aggregates in multidose protein formulations. Herein we investigated the efficiency of PEGylation (attachment of poly(ethylene glycol)) to prevent benzyl alcohol-induced aggregation of the model protein
Xi-Sha Zhang et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(50), 16214-16225 (2012-10-20)
We report three transformations: 1) direct transformation from biarylmethanols into biarylmethylamines; 2) direct transformation from one biarylmethanol into another biarylmethanol; 3) direct transformation from allylic alcohols into allylic amines. These transformations are based on pyridyl-directed Rh-catalyzed C-C bond cleavage of secondary alcohols and
Endea J Curry et al.
Dermatitis : contact, atopic, occupational, drug, 16(4), 203-208 (2006-03-16)
Benzyl alcohol is a weak sensitizer found in a wide array of plants and plant products, foods, cosmetics, and medications. Delayed contact dermatitis reactions as well as immediate, urticarial, and systemic reactions have been reported to occur with its use
H Ahumada et al.
The journal of physical chemistry. A, 109(30), 6644-6651 (2006-07-13)
Most drugs have to cross cell membranes to reach their final target. A better understanding of the distribution, interactions, and dynamics of biologically active molecules in model bilayers is of fundamental importance in understanding drug functioning and design. 2H NMR
Tatiana Mitkina et al.
Organic & biomolecular chemistry, 10(17), 3556-3561 (2012-03-27)
The oxidative coupling of sp(3) hybridized carbon atoms by photocatalysis is a valuable synthetic method as stoichiometric oxidation reagents can be avoided and dihydrogen is the only byproduct of the reaction. Cadmium sulfide, a readily available semiconductor, was used as
Rocky J Barney et al.
The Journal of organic chemistry, 76(8), 2875-2879 (2011-03-17)
Benzyl phosphonate esters often serve as reagents in Horner-Wadsworth-Emmons reactions. In most cases, they can be prepared from benzylic alcohols via formation of the corresponding halide followed by an Arbuzov reaction. To identify a more direct synthesis of phosphonate esters
Eric D Nacsa et al.
Journal of the American Chemical Society, 140(9), 3322-3330 (2018-02-06)
Nature routinely engages alcohols as leaving groups, as DNA biosynthesis relies on the removal of water from ribonucleoside diphosphates by a radical-mediated "spin-center shift" (SCS) mechanism. Alcohols, however, remain underused as alkylating agents in synthetic chemistry due to their low
P Cooper et al.
Biochimica et biophysica acta, 1139(1-2), 70-76 (1992-06-09)
Spin labelled (7-, 12- and 16- doxylsteric (DS) acid) erythrocyte (red blood cell) membranes isolated from six malignant hyperthermia susceptible (MHS) and six malignant hyperthermia normal (MHN) volunteer donors were characterized using the order parameter (S) and rotational correlation time
D E Rickert et al.
Biochemical pharmacology, 34(23), 4163-4168 (1985-12-01)
Previous work has suggested that quantitative differences in the in vitro and in vivo metabolism of mononitrotoluene isomers are a result of differences in the hepatic conjugation and oxidation of the first metabolic intermediates, the mononitrobenzyl alcohols. We have determined
Xiang Liu et al.
ChemSusChem, 6(4), 604-608 (2013-03-28)
Clean alcohol-alcohol cross-coupling: A clean and efficient one-pot direct C-C cross-coupling of equimolar amounts of primary and secondary alcohols by a facile hydrogen autotransfer pathway is achieved over a robust and easily recovered hydrotalcite-supported Au-Pd bimetallic catalyst system. A variety
Benzyl alcohol: a covert fragrance.
Sharon E Jacob et al.
Dermatitis : contact, atopic, occupational, drug, 18(4), 232-233 (2007-11-21)
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