Relevant bibliographies by topics / Alcohol synthesis

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Alcohol synthesis'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Alcohol synthesis"

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Zhyznevskiy, Vyacheslav, Volodymyr Gumenetskiy, Olena Shyshchak, and Yevhen Fedevych. "The use of isobutyl alcohol for methacrylate synthesis." Chemistry & Chemical Technology 5, no. 3 (September 15, 2011): 277–84. http://dx.doi.org/10.23939/chcht05.03.277.

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Sohilait, Hanoch J., Hardjono Sastrohamidjojo, and Sabirin Matsjeh. "SYNTHESIS OF SECONDARY ALCOHOL COMPOUNDS FROM SAFROLE AND METHYLEUGENOL." Indonesian Journal of Chemistry 3, no. 3 (June 9, 2010): 176–78. http://dx.doi.org/10.22146/ijc.21885.

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Synthesis of secondary alcohols compound from safrole and methyleugenol has been achieved through conversion of allyl group to alcohol.The reaction of safrole and methyleugenol with mercuric acetate in aqueous tetrahydrofuran, followed by in situ reduction of the mercurial intermediate by alkaline sodium borohydride produced secondary alcohol namely safryl alcohol (71.25%) and methyleugenil alcohol (65.56%). The structure elucidation of these products were analyzed by FTIR, 1H-NMR, 13C-NMR and MS. Keywords: Secondary alcohols; safrole; methyleugenol
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Honmute, Sindhu, Arunkumar Lagashetty, and A. Venkataraman A. Venkataraman. "Synthesis and Characterisation of Polyaniline-Polyvinyl Alcohol-NiO Nanocomposite Film." Indian Journal of Applied Research 3, no. 8 (October 1, 2011): 91–93. http://dx.doi.org/10.15373/2249555x/aug2013/29.

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Fediv, V. I. "Synthesis route and optical characterization of CdS:Mn/polyvinyl alcohol nanocomposite." Semiconductor Physics Quantum Electronics and Optoelectronics 15, no. 2 (May 30, 2012): 117–23. http://dx.doi.org/10.15407/spqeo15.02.117.

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Bildi, Özge Ceren, Barış Şimşek, and Osman Nuri Şara. "SYNTHESIS AND CHARACTERIZATION OF POLYVINYL ALCOHOL/CALCIUM CARBONATE COMPOSITE FILM." E-journal of New World Sciences Academy 15, no. 2 (April 30, 2020): 49–53. http://dx.doi.org/10.12739/nwsa.2020.15.2.3a0096.

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Milosavljevic, Milutin, Aleksandar Marinkovic, Jelena Markovic, Danijela Brkovic, and Milan Milosavljevic. "Synthesis of tetraalkyl thiuram disulfides using different oxidants in recycling solvent mixture." Chemical Industry and Chemical Engineering Quarterly 18, no. 1 (2012): 73–81. http://dx.doi.org/10.2298/ciceq110726048m.

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A new optimized laboratory synthesis of tetraalkyl thiuram disulfides, starting from dialkyl amines and carbon disulfide in presence of three oxidants (hydrogen peroxide, potassium peroxodisulfate and sodium hypochlorite) and appropriate reaction medium: two mixtures of isopropyl alcohol - water used in two consecutive syntheses, was presented in this work. First synthesis was performed in a recycled azeotropic mixture of isopropyl alcohol - water 87.7% - 12.3%, and second in a filtrate obtained after first synthesis, which was a mixture of isopropyl alcohol - water 70.4% - 29.6%. After the second synthesis and filtration, recycled azeotropic mixture isopropyl alcohol - water 87.7% - 12.3% was regenerated from the filtrate by rectification. Considering this, the technology for beneficial use of recycling isopropyl alcohol - water mixture as reaction medium for tetraalkyl thiuram disulfides synthesis was developed. Such concept contributes to extraordinary economical benefit of implemented optimal laboratory synthesis at semi-industrial level. High yields of tetraalkyl thiuram disulfides syntheses were obtained at both laboratory and semiindustrial level. Structure and purity of synthesized compounds were confirmed by elemental analysis, as well as FTIR, 1H and 13C NMR, and MS spectral data.
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Dong, Xu, Xiao Hui Zhang, Ming Hui Zhou, Wen Huan Wang, and Jing Chang Wang. "Synthesis of Guerbet Alcohol Acrylate Aided by Microwave." Advanced Materials Research 860-863 (December 2013): 1007–11. http://dx.doi.org/10.4028/www.scientific.net/amr.860-863.1007.

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Guerbet alcohol acrylate was synthesized using acrylic acid and guerbet alcohol alcohols as reactants, p-toluenesulfonic acid as catalyst, hydroquinone as polymerization inhibitor and toluol as solvent by microwave irradiation heating instead of the conventional heating with oil bath. The structure of product was characterized by FT-IR, 1H-NMR, 13C-NMR and the effect of different reaction parameters was discussed in this paper. A procedure for the generation of fairly clean guerbet alcohol acrylate is well developed and the results indicated that under the appropriate reaction conditions the esterification rate of guerbet alcohol acrylate could be achieved above 98%.
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Mishra, Satyendra, and Sejal Patel. "Design, Synthesis, and Anti-bacterial Activity of Novel Deoxycholic Acid- Amino Alcohol Conjugates." Medicinal Chemistry 16, no. 3 (April 17, 2020): 385–91. http://dx.doi.org/10.2174/1573406415666190206231002.

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Background: Numerous synthetic bile acid derivatives have been recognized for their various biological activities. Among these, bile acid amides have emerged as an attractive antibacterial agent. We herein illustrate the synthesis and antibacterial evaluation of deoxycholic acidamino alcohols conjugates. Objective: Design and Synthesis of novel deoxycholic acid-amino alcohol conjugates to investigate their antibacterial activity against E. coli and S. aureus. Methods: Novel deoxycholic acid-amino alcohol conjugates were synthesized, from conjugation of deoxycholic acid-NHS ester with amino alcohols. Various amino alcohols moieties were appended to the C24 position of deoxycholic acid to yield deoxycholic acid-amino alcohol conjugates. All the synthesized compounds were characterized by 1H NMR, 13C NMR, IR and massspectroscopy. The entire synthesized deoxycholic acid-amino alcohol conjugates were evaluated for their antibacterial activity against E. coli and S. aureus using the broth dilution method. Results: The outcome illustrated that some of the novel deoxycholic acid-amino alcohol conjugates exhibited enhanced anti-bacterial activities. Amongst them, deoxycholic acid-amino alcohol conjugate containing (-R)-2-aminocyclohexanol (1) demonstrated promising efficacy against both strains S. aureus ATCC 25923 (MIC 15 μg/mL) and E. coli ATCC 25922 (MIC 45 μg/mL) and was identified as a lead molecule. Conclusion: Numbers of novel deoxycholic acid-amino alcohol conjugates were synthesized and their antimicrobial activities provided useful information that the potency was strongly depending on the structures of deoxycholic acid-amino alcohol conjugates.
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Forzatti, Pio, Enrico Tronconi, and Italo Pasquon. "Higher Alcohol Synthesis." Catalysis Reviews 33, no. 1-2 (February 1991): 109–68. http://dx.doi.org/10.1080/01614949108020298.

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Lang, Charles H., Robert A. Frost, and Thomas C. Vary. "Skeletal muscle protein synthesis and degradation exhibit sexual dimorphism after chronic alcohol consumption but not acute intoxication." American Journal of Physiology-Endocrinology and Metabolism 292, no. 6 (June 2007): E1497—E1506. http://dx.doi.org/10.1152/ajpendo.00603.2006.

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Epidemiological evidence suggests alcoholic myopathy is more severe in females than males, but comparable animal studies are lacking that make elucidating the biochemical locus for this defect problematic. The present study determined whether skeletal muscle protein synthesis and markers of degradation exhibit a sexual dimorphic response to either chronic alcohol consumption or acute intoxication. Male and female rats were fed an alcohol-containing diet, pair-fed for 26 wk (chronic), or received an intraperitoneal injection of alcohol (acute). In males, chronic alcohol decreased gastrocnemius protein synthesis by 20%. This reduction was associated with a twofold increase in the inactive eukaryotic initiation factor (eIF) 4E·4E-binding protein 1 (4E-BP1) complex and a 60% reduction in the active eIF4E·eIF4G complex. This redistribution of eIF4E was associated with decreased phosphorylation of both 4E-BP1 and eIF4G (50–55%). The phosphorylation of ribosomal protein S6 was also reduced 60% in alcohol-consuming male rats. In contrast, neither rates of protein synthesis nor indexes of translation initiation in muscle were altered in alcohol-fed female rats despite blood alcohol levels comparable to males. Chronic alcohol ingestion did not alter atrogin-1 or muscle RING finger-1 mRNA content (biomarkers of muscle proteolysis) in males but increased their expression in females 50–100%. Acute alcohol intoxication produced a comparable decrease in muscle protein synthesis and translation initiation in both male and female rats. Our data demonstrate a sexual dimorphism for muscle protein synthesis, translation initiation, and proteolysis in response to chronic, but not acute, alcohol intoxication; however, they do not support evidence indicating females are more sensitive toward the development of alcoholic skeletal muscle myopathy.
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Dissertations / Theses on the topic "Alcohol synthesis"

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Sumer, Burak. "Synthesis Of 1,2-amino Alcohols Having Tertiary Alcohol Moiety." Master's thesis, METU, 2006. http://etd.lib.metu.edu.tr/upload/12607276/index.pdf.

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An applicable method for the racemic synthesis of 1,2-amino alcohols having tertiary alcohol moiety was developed. This method can be used as a general method for the synthesis of various 1,2-amino alcohols with various tertiary alcohol moieties by changing chloroacetone with different monohalo ketones, and with different aryl halides or alkyl halides. The resultant racemic 1,2-aminoe alcohols were tried to resolve by using various hydrolase type enzymes under different conditions by changing the parameters i.e. solvent, temperature and substrate: enzyme ratios. Finally, poorly resolved amino alcohol 20 with 21 % was used as chiral ligand in diethyl zinc reaction to benzaldhyde and afforded (R)-1-phenylpropan-1-ol almost with 21 % e.e..
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Imbault, Alexander Luis. "Alcohol synthesis using metal phosphides." Thesis, University of British Columbia, 2015. http://hdl.handle.net/2429/53655.

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Biofuels make up to 10wt% of gasoline sold in the United States of America and Canada, the largest portion of these biofuel additives is ethanol. Past research working with MoP/SiO₂ using syn gas (H₂:CO 1:1) as a feed have shown how an effective oxygenate catalyst can be promoted with K to become more selective towards ethanol. In this thesis, various metal phosphide catalysts including CoP, Co₂P, RuP and Fe₂P (all supported on SiO₂) are investigated using molecular modelling and activity tests with syn gas to find an effective oxygenate catalyst which can be understood and ultimately converted into an effective ethanol catalyst. Molecular modelling is performed on metal phosphide catalysts to determine the CO adsorption strengths of several metal phosphide catalysts. The correlation between the adsorption energies and oxygenate formation is then examined. Fe₂P is shown to be a catalyst of interest for its ability to create sizable amounts of methanol and other oxygenates, and it has a moderate CO adsorption strength. The second focus of this thesis is on the effects of passivation on two metal phosphide catalysts, MoP/SiO₂ and Ni₂P/SiO₂. This is investigated through measuring H₂ uptake during TPR and CO uptake during CO chemisorption after different passiviiation techniques. The results of these measurements finds that Ni₂P/SiO₂ and MoP/SiO₂ react very differently after being kept out of contact with air, passivated in a low flow of O₂ or being exposed to ambient air after reduction.
Applied Science, Faculty of
Chemical and Biological Engineering, Department of
Graduate
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Nguyen, Thi-Ngoc Dieu. "Allylsilanes in organic synthesis homoallylic alcohol synthesis and electrophilic alkylation." Thesis, McGill University, 1992. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=60726.

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The chelating effect on regio- and stereochemical control of the homoallyl alcohol synthesis and electrophilic substitution of allylsilane was studied, using 2,2-dimethyl-1-$ {$1- ((S)-2-(2-methoxyethoxy)methyl) pyrrolidinyl$ }$-2-sila-4-pentene (S1) and 2,2-Dimethyl-1-$ {$1- ((S)-2-hydroxymethyl) pyrrolidinyl$ !$-2-sila-4-pentene (S2), with S1 synthesized from L-Prolinol.
The synthesis of homoallyl alcohol was carried out by allyl transformation from S1 and S2 to a Lewis acid activated aldehyde. Chelation between the allylsilyl ligand and the Lewis acid:aldehyde complex was found to favor the cyclic syn-clinal over the acyclic anti-periplanar transition state, in the asymmetric synthesis of the alcohol 1-dodecen-4-ol (P1). The bulky, remote and weak chelating ligand resulted in only modest selectivity and average chemical yield.
Regio- and stereochemical control of the electrophilic alkylation of allylsilanes S1 were achieved due to chelating effect that favored $ alpha$-alkylation. The chiral chelating ligand also resulted in enhanced stereochemical control electrophilic alkylation. Steric effect, due to a large electrophile, and solvent effect that causes disruption of the chelated complex, decrease $ alpha$-selectivity.
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Lue, Bena-Marie. "Biosynthesis of phenolic lipid models using oleyl alcohol and triolein." Thesis, McGill University, 2004. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=80324.

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The overall objective of this study was the optimization of a model enzymatic system in organic solvent media for the biosynthesis of selected phenolic lipid compounds. The model enzymatic system consisted of cinnamic acid and oleyl alcohol as substrates using commercial immobilized lipase (Novozym 435) from Candida antarctica. The experimental findings showed that an increase in the hydrophobicity of the solvent mixture and a decrease in the aw values of the reaction medium increased the initial enzymatic activity and bioconversion yield; the use of an iso-octane and butanone solvent mixture (85:15, v/v) and an initial aw of 0.05 resulted in an initial enzymatic activity of 192.7 nmol product/g enzyme/min and a corresponding bioconversion yield of 95.3% after a 16-day reaction period.
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Barks, Jenny Marie. "Stereoselective tetrahydrofuran synthesis." Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307740.

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Zaman, Sharif Fakhruz. "An investigation of MoP catalysts for alcohol synthesis." Thesis, University of British Columbia, 2010. http://hdl.handle.net/2429/23165.

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Molecular simulation and experimental methods have been used to assess the catalytic behavior of MoP in the conversion of synthesis gas (CO, CO₂, H₂) to oxygenated hydrocarbons. The potential energy surface of synthesis gas conversion to methane and methanol was investigated on a Mo₆P₃ cluster model of the MoP catalyst. The potential energy surface (PES) for CH₄ formation was determined to be: COad → CHOad → CH₂Oad → CH₂OHad → CH₂.ad+H₂Oad → CH₃.ad+H₂Oad → CH₄+H₂O and for CH₃OH : COad → CHOad → CH₂Oad → CH₂OHad → CH₃OHad. The hydroxymethyl (CH₂OH) species was a common reaction intermediate for both CH₄ and CH₃OH formation and the simulation predicted selective formation of CH₄ rather than CH₃OH from syngas over MoP. The cluster model was modified to investigate the effect of a SiO₂ support and a K promoter. Both SiO₂ and K decreased the activation energy for methanol formation. However, the activation energy for methanol formation remained higher than the activation energy for C-O bond cleavage. The high adsorption energy of methanol and the formation of geminal dicarbonyl species on the K-Mo₆P₃-Si₃O₉ cluster suggested the possibility of the formation of higher oxygenates. The conversion of syngas to alcohols was also investigated on 5, 10, and 15 wt% MoP supported on silica, with 0, 1, and 5 wt% K added as a promoter The major products were acetaldehyde, acetone and ethanol. Low selectivities to methanol (<5 C atom %) and methane (< 10 C atom%) were observed on the 5%K-10%MoP-SiO₂ catalyst. The product distribution obtained over the K-MoP/SiO₂ catalyst was distinct from that reported in the literature over other Mo-based catalysts. Addition of Rh to the K-MoP/SiO₂ catalyst improved the stability of the catalyst. However, the Rh increased the selectivity to hydrocarbon products, especially CH4, while only increasing the selectivity to ethanol marginally. The reaction kinetics of the major products were described by a simple empirical power law. The activation energies of ethanol and acetaldehyde were very similar, suggesting that both originated from the same surface intermediate.
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Loveridge, Tracey. "Chiral chromium complexes in synthesis." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296868.

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Safinski, Tomasz School of Chemical Engineering &amp Industrial Chemistry UNSW. "Catalytic distillation for the synthesis of tertiary butyl alcohol." Awarded by:University of New South Wales. School of Chemical Engineering and Industrial Chemistry, 2005. http://handle.unsw.edu.au/1959.4/23068.

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Catalytic Distillation for the synthesis of tertiary butyl alcohol (TBA) is investigated in this thesis. The solvent, ethylene glycol, is proposed as a means of overcoming challenges, which limit the potential benefits of the application of reactive separation for TBA. The proposed action of the solvent is that of extractive distillation entrainer, thus a new unit operation of Catalytic Extractive Distillation (CED) is suggested. The solubility of isobutylene in water, TBA, and ethylene glycol and their binary and ternary mixtures, at different temperatures, is measured and correlated. The solubility is found to be highly non-linear in solutions containing TBA. The kinetics of isobutylene hydration over Amberlyst 15 is characterised in the presence of ethylene glycol. The solvent is found to promote reaction rate, however it is also found to compete for reaction with isobutylene. Water is found to strongly inhibit the reaction of ethylene glycol and isobutylene. The selectivity ratio of TBA to by products is determined and found to improve with increased temperature and lower solvent concentration. Bale packing is chosen as catalytic distillation hardware for the containment of Amberlyst 15 and its two-phase fluid dynamics characterised for the first time. Raschig rings are used as a benchmark for the study. Bale packing is found to exhibit two ranges of backmixing behaviour in the pre-loading regime. This behaviour is attributed to the three levels of porosity of the hardware and indicative of low rates of catalyst/liquid renewal. The effectiveness of ethylene glycol as extractive distillation entrainer for the separation of the TBA/water azeotrope over Bale packing is investigated and the solvent found to be highly effective. The mass transfer resistances to isobutylene transport are determined for countercurrent fixed bed reactor (CFBR) application of Bale packing. It is found that ethylene glycol improves mass transfer coefficients attainable. Catalytic Extractive Distillation is implemented over Bale packing and the ability of the solvent to improve reaction rates and purity of TBA demonstrated. However, the reaction rates achieved have much scope for improvement through increased isobutylene availability. In response to poor liquid renewal of static packing such as Bale packing and the necessity of improved isobutylene transport a new form of catalytic distillation reactor design is proposed, the Basket Impeller Column (BIC). The BIC combines the mass transfer benefits of a rotating basket reactor with that of a dual flow column. Capacity of the new hardware is determined and correlated. Separation and reactive separation are demonstrated to be feasible. It is found that Damk??hler number can be varied directly using the additional process variable of speed of rotation.
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McLaughlin, M. G. "Highly selective hydrometallations and their application in synthesis." Thesis, Queen's University Belfast, 2014. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.679265.

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Bayir, N. "Modelling of integrated de-novo pathways for amino alcohol synthesis." Thesis, University College London (University of London), 2017. http://discovery.ucl.ac.uk/1561249/.

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Chiral amino alcohols are industrially valuable intermediates used in the synthesis of many pharmaceuticals and fine chemicals. Transamination (TAm) is not only one of the most interesting industrial enzymatic reactions on its own nowadays but also the second enzymatic step of the de novo pathway studied by our research group (Bioconversion-Chemistry and Engineering Interface Programme-BiCE) for the synthesis of chiral amino alcohols. In this thesis, firstly a study on the kinetic modelling of TAm reactions was presented. Kinetic behaviour of two ω-TAm reactions employing different amino acceptors but the same amino donor was investigated. Using a Genetic Algorithm, kinetic models could be determined with only 10-12 progress curves for both reaction schemes without having any experimental data for the reverse reaction. Also, a sensitivity analysis on the kinetic parameters of both reactions was carried out. Having gained enough insight into the kinetic modelling of TAm reactions, two different sequential enzyme reactions leading to the synthesis of 2-amino-1,3,4- butanetriol (ABT) were studied. The first one involved three different enzymes, namely TAm (pQR977), Transketolase (TK) and TAm (pQR801). 100% conversion was proven possible with both experimental and simulation results in a 28 hour-long fed-batch reaction. Although, the concentrations tested in the experiments were low, this three-step sequential enzyme reaction showed great promise for further being optimized for industrial applications. The second one was a recycling sequential enzyme reaction involving three different enzymatic reactions taking place simultaneously. Two of the reactions were catalyzed by TAm (pQR1021) and one of them was catalyzed by TK. With the help of second TAm reaction not only desired product was synthesized but also one of the intermediary precursors was recycled within the system. The long term goal of this project was the integration of de novo pathways leading to the synthesis of chiral amino alcohols into host cell metabolism. Thus, the recycling sequential enzyme reaction employing only two different enzymes and two different substrates was found promising for achieving this goal. With both experimental and simulation results the favorability of this reaction was demonstrated and low amounts of ABT (~6 mM) was synthesized in a 8-hour long reaction using purified enzymes. One of the precursors in both sequential enzyme reactions was serine. In the final results chapter, a metabolic modelling methodology was used for identifying optimal metabolic engineering strategies, namely enzyme knock-outs and enzyme expression level modulations, for the overproduction of serine by employing a partial mechanistic model of central carbon metabolism of Escherichia coli. Simulation results showed 89% increase in serine synthesis in the case of doubling the expression level of SerSynth, a hypothetical enzyme for the synthesis of serine from 3-phosphoglycerate.
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Books on the topic "Alcohol synthesis"

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Cardona, C. A. Process synthesis for fuel ethanol production. Boca Raton: Taylor & Francis, 2010.

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J, Sanchez O., and Gutierrez L. F, eds. Process synthesis for fuel ethanol production. Boca Raton: Taylor & Francis, 2010.

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Cardona, C. A. Process synthesis for fuel ethanol production. Boca Raton: Taylor & Francis, 2010.

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Wang, Yaquan. New routes to Rh (and CeO2-Promoted) Rh/SiO2 catalysts for alcohol synthesis. Uxbridge: Brunel University, 1994.

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Psychodynamics of alcoholism: A current synthesis. Springfield, Ill., U.S.A: Thomas, 1986.

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International Conference on Global Impacts of Applied Microbiology (7th 1985 Helsinki, Finland). GIAM VII symposia, alcohol fermentation, plant cell culture: Proceedings of seventh International Conference on Global Impacts of Applied Microbiology : symposia on alcohol fermentation and plant cell culture, August 14-15, 1985, Helsinki, Finland. Helsinki, Finland: Foundation for Biotechnical and Industrial Fermentation Research, 1986.

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Toivari, Mervi. Engineering the pentose phosphate pathway of Saccharomyces cerevisiae for production of ethanol and xylitol. [Espoo, Finland]: VTT Technical Research Centre of Finland, 2007.

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1947-, Russell Inge, and Stewart Graham G. 1942-, eds. Thermophilic microbes in ethanol production. Boca Raton, Fla: CRC Press, 1987.

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Palmer, Matthew Jon. The stereoselective synthesis of alcohols. [s.l.]: typescript, 1997.

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Francis, Stephen R. Staff report: Initial statement of reason for rulemaking : public hearing to consider adoption of specifications for alternative fuels for motor vehicles. [Sacramento]: State of California, Air Resources Board, Stationary Source Divison, 1991.

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Book chapters on the topic "Alcohol synthesis"

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Vary, Thomas C., and Charles H. Lang. "Assessing Effects of Alcohol Consumption on Protein Synthesis in Striated Muscles." In Alcohol, 343–55. Totowa, NJ: Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-242-7_22.

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Rothschild, M. A., M. Oratz, and S. S. Schreiber. "Alcohol Effects on Albumin Synthesis." In Alcohol Related Diseases in Gastroenterology, 96–105. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70048-4_5.

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Lin, Teng-nan, and Grace Y. Sun. "Synthesis of Fatty Acid Ethyl Esters by Brain Membranes." In Molecular Mechanisms of Alcohol, 107–18. Totowa, NJ: Humana Press, 1989. http://dx.doi.org/10.1007/978-1-4612-4514-8_9.

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Duester, Gregg. "Involvement of Alcohol-Metabolizing Enzymes in Retinoic Acid Synthesis and Inhibition by Ethanol." In Alcohol and Hormones, 75–95. Totowa, NJ: Humana Press, 1995. http://dx.doi.org/10.1007/978-1-4612-0243-1_4.

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Geerlof, A., J. B. A. Tol, J. A. Jongejan, and J. A. Duine. "Microbial Alcohol/Aldehyde Oxidoreductases in Enantioselective Conversions." In Microbial Reagents in Organic Synthesis, 411–20. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2444-7_33.

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Han, Feng, Wei Sun, Chungu Xia, and Chao Liu. "Alcohol as a Reagent in Homogeneous Catalysis." In Solvents as Reagents in Organic Synthesis, 403–47. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527805624.ch10.

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Brückner, Christian. "Nitroxide-Catalyzed Alcohol Oxidations in Organic Synthesis." In Stable Radicals, 433–60. Chichester, UK: John Wiley & Sons, Ltd, 2010. http://dx.doi.org/10.1002/9780470666975.ch12.

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Hummel, Werner. "New alcohol dehydrogenases for the synthesis of chiral compounds." In New Enzymes for Organic Synthesis, 145–84. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/bfb0103304.

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Kuwabata, Susumu, Ruo Yuan, Shozo Watanabe, and Hiroshi Yoneyama. "Electroorganic Synthesis of Optically Active Alcohols from Ketone and Aldehyde Derivatives Using Alcohol Dehydrogenase as an Electrocatalyst." In Novel Trends in Electroorganic Synthesis, 205–8. Tokyo: Springer Japan, 1998. http://dx.doi.org/10.1007/978-4-431-65924-2_62.

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Lemière, G. L. "Alcohol Dehydrogenase Catalysed Oxidoreduction Reactions in Organic Chemistry." In Enzymes as Catalysts in Organic Synthesis, 19–34. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4686-6_2.

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Conference papers on the topic "Alcohol synthesis"

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Jiang, Xiaofei, Ying Zhang, Yunzheng Li, Qingshan Zhang, and Hongquan Yin. "Synthesis of Prenyl Alcohol from Isoprene." In 2015 International Symposium on Energy Science and Chemical Engineering. Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/isesce-15.2015.22.

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Rai, Sumit Kumar, and Piyali Basak. "Synthesis and characterization of polyvinyl alcohol hydrogel." In 2010 International Conference on Systems in Medicine and Biology (ICSMB). IEEE, 2010. http://dx.doi.org/10.1109/icsmb.2010.5735404.

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Khanduri, Priya, Varij Panwar, Alankrita Joshi, and Lokesh Singh Panwar. "Synthesis and characterization of poly-vinyl alcohol membrane." In SECOND INTERNATIONAL CONFERENCE ON MATERIAL SCIENCE, SMART STRUCTURES AND APPLICATIONS: ICMSS-2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5141440.

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Mahendia, Suman, A. K. Tomar, Rishi Pal Chahal, Shyam Kumar, Alka B. Garg, R. Mittal, and R. Mukhopadhyay. "Synthesis and Characterization of Silver-Poly(vinyl alcohol) Nanocomposites." In SOLID STATE PHYSICS, PROCEEDINGS OF THE 55TH DAE SOLID STATE PHYSICS SYMPOSIUM 2010. AIP, 2011. http://dx.doi.org/10.1063/1.3605873.

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Yuan Haoran, Zhao Dandan, Xiong Zuhong, Chen Yong, and Ma Longlong. "Thermodynamic and Experimental Study on Alcohol Made by Synthesis Gas." In Environment (ICMREE). IEEE, 2011. http://dx.doi.org/10.1109/icmree.2011.5930535.

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Nasir, Muhamad, Juliandri, and Rizky Ahsan Ansharullah. "Synthesis of copper acetate/polyvinyl alcohol nanofiber composite by electrospinning." In 2017 IEEE 7th International Conference "Nanomaterials: Application & Properties" (NAP). IEEE, 2017. http://dx.doi.org/10.1109/nap.2017.8190263.

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Maruyama, S., Y. Miyauchi, Y. Murakami, and S. Chiashi. "CONTROLLED CVD SYNTHESIS OF SINGLE-WALLED CARBON NANOTUBES FROM ALCOHOL." In Annals of the Assembly for International Heat Transfer Conference 13. Begell House Inc., 2006. http://dx.doi.org/10.1615/ihtc13.p8.250.

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Mizoguchi, M., C. Sakai, A. Nakamura, and J. Temmyo. "Direct Synthesis of Graphene films via Alcohol CVD for Transparent Electrode." In 2013 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2013. http://dx.doi.org/10.7567/ssdm.2013.p-5-4l.

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Naydenova, Vessela, Vasil Iliev, Maria Kaneva, Georgi Kostov, Petia Koprinkova-Hristova, and Silviya Popova. "Modeling Of Alcohol Fermentation In Brewing – Carbonyl Compounds Synthesis And Reduction." In 28th Conference on Modelling and Simulation. ECMS, 2014. http://dx.doi.org/10.7148/2014-0279.

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Ozcan, Arif, and Emine Arman Kandirmaz. "POLY[(VINYL ALCOHOL) - (STEARIC ACID)] SYNTHESIS AND USE IN LAVENDER OIL CAPSULATION." In 9th International Symposium on Graphic Engineering and Design. Faculty of Technical Sciences, 2018. http://dx.doi.org/10.24867/grid-2018-p23.

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Reports on the topic "Alcohol synthesis"

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Gerber, Mark A., James F. White, and Don J. Stevens. Mixed Alcohol Synthesis Catalyst Screening. Office of Scientific and Technical Information (OSTI), September 2007. http://dx.doi.org/10.2172/926119.

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Blackmond, D. G., I. Wender, R. Oukaci, and J. Wang. Probe molecule studies: Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), July 1992. http://dx.doi.org/10.2172/7154553.

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Blackmond, D. G., I. Wender, R. Oukaci, and J. Wang. Probe molecule studies: Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/6758736.

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Ms. Xiaolei Sun and Professor George W. Roberts. PROMOTED ZINC CHROMITE CATALYSTS FOR HIGHER ALCOHOL SYNTHESIS. Office of Scientific and Technical Information (OSTI), December 2000. http://dx.doi.org/10.2172/783704.

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Ms. Xiaolei Sun and Professor George W. Roberts. PROMOTED ZINC CHROMITE CATALYSTS FOR HIGHER ALCOHOL SYNTHESIS. Office of Scientific and Technical Information (OSTI), June 2000. http://dx.doi.org/10.2172/781794.

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Ms. Xiaolei Sun and Professor George W. Roberts. PROMOTED ZINC CHROMITE CATALYSTS FOR HIGHER ALCOHOL SYNTHESIS. Office of Scientific and Technical Information (OSTI), August 2000. http://dx.doi.org/10.2172/781795.

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Blackmond, D. G. Probe molecule studies: Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), April 1992. http://dx.doi.org/10.2172/5100318.

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Gerber, Mark A., J. F. White, Michel J. Gray, and Don J. Stevens. Mixed Alcohol Synthesis Catalyst Screening 2007 Progress Report. Office of Scientific and Technical Information (OSTI), November 2007. http://dx.doi.org/10.2172/926120.

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Blackmond, D. G., I. Wender, R. Oukaci, and J. Wang. Probe molecule studies: Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), October 1992. http://dx.doi.org/10.2172/6873487.

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Blackmond, D. G., and I. Wender. Probe molecule studies: Active species in alcohol synthesis. Office of Scientific and Technical Information (OSTI), September 1991. http://dx.doi.org/10.2172/6128128.

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You might also be interested in the extended bibliographies on the topic 'Alcohol synthesis' for particular source types:
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