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You searched for subject:(Ortho quinone m thyde). Showing records 1 – 30 of 6063 total matches.

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University of New South Wales

1. Hong, Kam. Synthesis of chromene based natural products.

Degree: Chemistry, 2016, University of New South Wales

 The primary aim of this project was to develop total syntheses of natural products kamalachalcone A and rottlerin, as their syntheses have never been reported.… (more)

Subjects/Keywords: Ortho-quinone methide; Rottlerin; Kamalachalcone A

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APA (6th Edition):

Hong, K. (2016). Synthesis of chromene based natural products. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/56351 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40600/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Hong, Kam. “Synthesis of chromene based natural products.” 2016. Doctoral Dissertation, University of New South Wales. Accessed January 27, 2021. http://handle.unsw.edu.au/1959.4/56351 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40600/SOURCE02?view=true.

MLA Handbook (7th Edition):

Hong, Kam. “Synthesis of chromene based natural products.” 2016. Web. 27 Jan 2021.

Vancouver:

Hong K. Synthesis of chromene based natural products. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2021 Jan 27]. Available from: http://handle.unsw.edu.au/1959.4/56351 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40600/SOURCE02?view=true.

Council of Science Editors:

Hong K. Synthesis of chromene based natural products. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/56351 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40600/SOURCE02?view=true


University of Adelaide

2. Spence, Justin Thomas James. Biomimetic synthesis of natural products via reactions of ortho-quinone methides.

Degree: 2016, University of Adelaide

 In recent times, natural product synthesis has become central to many scientific fields; from chemistry, through to biology and pharmacology. As synthetic chemists, natural products… (more)

Subjects/Keywords: natural product synthesis; biomimetic synthesis; ortho-quinone methides

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APA (6th Edition):

Spence, J. T. J. (2016). Biomimetic synthesis of natural products via reactions of ortho-quinone methides. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/102583

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Spence, Justin Thomas James. “Biomimetic synthesis of natural products via reactions of ortho-quinone methides.” 2016. Thesis, University of Adelaide. Accessed January 27, 2021. http://hdl.handle.net/2440/102583.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Spence, Justin Thomas James. “Biomimetic synthesis of natural products via reactions of ortho-quinone methides.” 2016. Web. 27 Jan 2021.

Vancouver:

Spence JTJ. Biomimetic synthesis of natural products via reactions of ortho-quinone methides. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/2440/102583.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Spence JTJ. Biomimetic synthesis of natural products via reactions of ortho-quinone methides. [Thesis]. University of Adelaide; 2016. Available from: http://hdl.handle.net/2440/102583

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

3. Cassagnes, Laure-Estelle. Cycle redox quinone-quinone réductase 2 et conséquences sur la production d'espèces oxygénées réactives dans le contexte cellulaire : Quinone-quinone reductase 2 redox cycle and consequences on the production of reactive oxygen species in the cellular context.

Degree: Docteur es, Chimie, biologie, santé, 2015, Université Toulouse III – Paul Sabatier

La quinone réductase 2 ou QR2 est une enzyme qui, comme son homologue QR1, joue un rôle de détoxification des quinones, molécules fortement réactives, en… (more)

Subjects/Keywords: Quinone réductase 2; Stress oxydant; RPE; Electrochimie; Ortho et para-quinones; Sonde redox; Quinone reductase 2; Oxidative stress; EPR; Electrochemistry; Ortho and para-quinones; Redox probe

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APA (6th Edition):

Cassagnes, L. (2015). Cycle redox quinone-quinone réductase 2 et conséquences sur la production d'espèces oxygénées réactives dans le contexte cellulaire : Quinone-quinone reductase 2 redox cycle and consequences on the production of reactive oxygen species in the cellular context. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2015TOU30148

Chicago Manual of Style (16th Edition):

Cassagnes, Laure-Estelle. “Cycle redox quinone-quinone réductase 2 et conséquences sur la production d'espèces oxygénées réactives dans le contexte cellulaire : Quinone-quinone reductase 2 redox cycle and consequences on the production of reactive oxygen species in the cellular context.” 2015. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed January 27, 2021. http://www.theses.fr/2015TOU30148.

MLA Handbook (7th Edition):

Cassagnes, Laure-Estelle. “Cycle redox quinone-quinone réductase 2 et conséquences sur la production d'espèces oxygénées réactives dans le contexte cellulaire : Quinone-quinone reductase 2 redox cycle and consequences on the production of reactive oxygen species in the cellular context.” 2015. Web. 27 Jan 2021.

Vancouver:

Cassagnes L. Cycle redox quinone-quinone réductase 2 et conséquences sur la production d'espèces oxygénées réactives dans le contexte cellulaire : Quinone-quinone reductase 2 redox cycle and consequences on the production of reactive oxygen species in the cellular context. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2015. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2015TOU30148.

Council of Science Editors:

Cassagnes L. Cycle redox quinone-quinone réductase 2 et conséquences sur la production d'espèces oxygénées réactives dans le contexte cellulaire : Quinone-quinone reductase 2 redox cycle and consequences on the production of reactive oxygen species in the cellular context. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2015. Available from: http://www.theses.fr/2015TOU30148

4. Montagut-Romans, Adrien. Réactivité et pharmacomodulation de la 4-hydroxycoumarine : conception, synthèse et évaluation biologique de nouvelles molécules rodonticides éco-compatibles : Reactivity and pharmacomodulation of 4-hydroxycoumarin : design, synthesis and biological evaluation of new eco-friendly rodenticide.

Degree: Docteur es, Chimie, 2014, Université Claude Bernard – Lyon I

L'usage des pesticides au sein de l'Union européenne est de plus en plus réglementé, et les rodonticides actuellement disponibles sur le marché sont responsables de… (more)

Subjects/Keywords: 4-hydroxycoyumarine; Anticoagulant; Rodonticide; Éco-compatible; Ortho-quinone méthyde; Catalyse homogène; Catalyse hétérogène; Pharmacomodulation; 4-hydroxycoumarin; Anticoagulant; Rodonticide; Eco-friendly; Ortho-quinone methyde; Homogeneous catalysis; Heterogeneous catalysis; Pharmacomodulation; 540

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APA (6th Edition):

Montagut-Romans, A. (2014). Réactivité et pharmacomodulation de la 4-hydroxycoumarine : conception, synthèse et évaluation biologique de nouvelles molécules rodonticides éco-compatibles : Reactivity and pharmacomodulation of 4-hydroxycoumarin : design, synthesis and biological evaluation of new eco-friendly rodenticide. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2014LYO10028

Chicago Manual of Style (16th Edition):

Montagut-Romans, Adrien. “Réactivité et pharmacomodulation de la 4-hydroxycoumarine : conception, synthèse et évaluation biologique de nouvelles molécules rodonticides éco-compatibles : Reactivity and pharmacomodulation of 4-hydroxycoumarin : design, synthesis and biological evaluation of new eco-friendly rodenticide.” 2014. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed January 27, 2021. http://www.theses.fr/2014LYO10028.

MLA Handbook (7th Edition):

Montagut-Romans, Adrien. “Réactivité et pharmacomodulation de la 4-hydroxycoumarine : conception, synthèse et évaluation biologique de nouvelles molécules rodonticides éco-compatibles : Reactivity and pharmacomodulation of 4-hydroxycoumarin : design, synthesis and biological evaluation of new eco-friendly rodenticide.” 2014. Web. 27 Jan 2021.

Vancouver:

Montagut-Romans A. Réactivité et pharmacomodulation de la 4-hydroxycoumarine : conception, synthèse et évaluation biologique de nouvelles molécules rodonticides éco-compatibles : Reactivity and pharmacomodulation of 4-hydroxycoumarin : design, synthesis and biological evaluation of new eco-friendly rodenticide. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2014. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2014LYO10028.

Council of Science Editors:

Montagut-Romans A. Réactivité et pharmacomodulation de la 4-hydroxycoumarine : conception, synthèse et évaluation biologique de nouvelles molécules rodonticides éco-compatibles : Reactivity and pharmacomodulation of 4-hydroxycoumarin : design, synthesis and biological evaluation of new eco-friendly rodenticide. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2014. Available from: http://www.theses.fr/2014LYO10028

5. Duncan, Julia Martha. Method Development Towards Catalytic Transformations of Reactive Intermediates.

Degree: 2020, University of Nevada – Reno

 This program focused largely on accessing highly reactive intermediates, including ortho-quinone methides (o-QMs) and benzylic carbocations, from simple and easily accessed starting materials. The primary… (more)

Subjects/Keywords: Carbocations; Lewis Acid Catalysis; Method Development; ortho-Quinone Methides; Piancatelli Rearrangement; Substitution

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APA (6th Edition):

Duncan, J. M. (2020). Method Development Towards Catalytic Transformations of Reactive Intermediates. (Thesis). University of Nevada – Reno. Retrieved from http://hdl.handle.net/11714/7408

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Duncan, Julia Martha. “Method Development Towards Catalytic Transformations of Reactive Intermediates.” 2020. Thesis, University of Nevada – Reno. Accessed January 27, 2021. http://hdl.handle.net/11714/7408.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Duncan, Julia Martha. “Method Development Towards Catalytic Transformations of Reactive Intermediates.” 2020. Web. 27 Jan 2021.

Vancouver:

Duncan JM. Method Development Towards Catalytic Transformations of Reactive Intermediates. [Internet] [Thesis]. University of Nevada – Reno; 2020. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/11714/7408.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Duncan JM. Method Development Towards Catalytic Transformations of Reactive Intermediates. [Thesis]. University of Nevada – Reno; 2020. Available from: http://hdl.handle.net/11714/7408

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Michigan

6. Dax, Scott Louis. New Methodology For The Generation Of Ortho-quinone Methides: Application To The Synthesis Of Cannabinoids.

Degree: PhD, Pure Sciences, 1986, University of Michigan

 Two general approaches for the generation of orthoquinone methides are described. These methods involve oxidations of ortho-substituted phenols and the 1,4-elimination of ortho-hydroxybenzylic alcohol derivatives.… (more)

Subjects/Keywords: Application; Cannabinoids; Generation; Methides; Methodology; New; Ortho; Quinone; Synthesis

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APA (6th Edition):

Dax, S. L. (1986). New Methodology For The Generation Of Ortho-quinone Methides: Application To The Synthesis Of Cannabinoids. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/127903

Chicago Manual of Style (16th Edition):

Dax, Scott Louis. “New Methodology For The Generation Of Ortho-quinone Methides: Application To The Synthesis Of Cannabinoids.” 1986. Doctoral Dissertation, University of Michigan. Accessed January 27, 2021. http://hdl.handle.net/2027.42/127903.

MLA Handbook (7th Edition):

Dax, Scott Louis. “New Methodology For The Generation Of Ortho-quinone Methides: Application To The Synthesis Of Cannabinoids.” 1986. Web. 27 Jan 2021.

Vancouver:

Dax SL. New Methodology For The Generation Of Ortho-quinone Methides: Application To The Synthesis Of Cannabinoids. [Internet] [Doctoral dissertation]. University of Michigan; 1986. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/2027.42/127903.

Council of Science Editors:

Dax SL. New Methodology For The Generation Of Ortho-quinone Methides: Application To The Synthesis Of Cannabinoids. [Doctoral Dissertation]. University of Michigan; 1986. Available from: http://hdl.handle.net/2027.42/127903

7. Boulven, Manon. Conception, synthèse et évaluation biologique de nouveaux composés hétérocycliques anticoagulants à usage rodonticide : Design, synthesis and biological evaluation of new anticoagulant heterocyclic compounds for rodenticide use.

Degree: Docteur es, Chimie organique, 2016, Lyon

A ce jour, les anticoagulants commerciaux souffrent de deux inconvénients majeurs : leur rémanence avec, pour certains d’entre eux, une demi-vie hépatique proche des 300… (more)

Subjects/Keywords: Chimie organique; Synthèse chimique; Anticoagulant; Lutte contre les rongeurs; Hétérocycle; 4-Hydroxycoumarine; Anti-Vitamine K; Ortho-Quinone méthide; Organic chemistry; Chemical synthesis; Anticoagulant; Rodent control; Heterocycle; 4-Hydroxycoumarin; Anti-Vitamin K; Ortho-Quinone methide; 547.507 2

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APA (6th Edition):

Boulven, M. (2016). Conception, synthèse et évaluation biologique de nouveaux composés hétérocycliques anticoagulants à usage rodonticide : Design, synthesis and biological evaluation of new anticoagulant heterocyclic compounds for rodenticide use. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2016LYSEI106

Chicago Manual of Style (16th Edition):

Boulven, Manon. “Conception, synthèse et évaluation biologique de nouveaux composés hétérocycliques anticoagulants à usage rodonticide : Design, synthesis and biological evaluation of new anticoagulant heterocyclic compounds for rodenticide use.” 2016. Doctoral Dissertation, Lyon. Accessed January 27, 2021. http://www.theses.fr/2016LYSEI106.

MLA Handbook (7th Edition):

Boulven, Manon. “Conception, synthèse et évaluation biologique de nouveaux composés hétérocycliques anticoagulants à usage rodonticide : Design, synthesis and biological evaluation of new anticoagulant heterocyclic compounds for rodenticide use.” 2016. Web. 27 Jan 2021.

Vancouver:

Boulven M. Conception, synthèse et évaluation biologique de nouveaux composés hétérocycliques anticoagulants à usage rodonticide : Design, synthesis and biological evaluation of new anticoagulant heterocyclic compounds for rodenticide use. [Internet] [Doctoral dissertation]. Lyon; 2016. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2016LYSEI106.

Council of Science Editors:

Boulven M. Conception, synthèse et évaluation biologique de nouveaux composés hétérocycliques anticoagulants à usage rodonticide : Design, synthesis and biological evaluation of new anticoagulant heterocyclic compounds for rodenticide use. [Doctoral Dissertation]. Lyon; 2016. Available from: http://www.theses.fr/2016LYSEI106

8. Karabaeva, Kanykey E. Photochemistry of Masked Pyrene-4,5-Dione.

Degree: MS, Chemistry, 2013, Bowling Green State University

 The photochemistry of 1,2-dipyridinium dihydrodioxin, 1,1-di(2-pyridyl) dihydrodioxin, 1,1-di(2-pyridyl) dihydrodioxin-Cu2+, pyrene-4,5-dione, and their complexes with DNA were studied. Also, quantum yields of pyrene-4,5-dione release from 1,2-dipyridinium… (more)

Subjects/Keywords: Chemistry; photochemistry; dihydrodioxin; ortho-quinone; caged molecule; DNA cutting agent; ultrafast

…22 2 Ortho-quinone Release from DHD… …good DNA cleaving agents. The ortho-quinone family is a big class of DNA-cutting agents… …Ortho-quinone reactivity is significant which makes their delivery to a targeted cell… …difficult, but masking the ortho-quinone with photosensitive masking group makes their delivery to… …of ortho-quinone by the mechanism outlined in Scheme 6. Scheme 5. Mechanism of electron… 

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APA (6th Edition):

Karabaeva, K. E. (2013). Photochemistry of Masked Pyrene-4,5-Dione. (Masters Thesis). Bowling Green State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1371083757

Chicago Manual of Style (16th Edition):

Karabaeva, Kanykey E. “Photochemistry of Masked Pyrene-4,5-Dione.” 2013. Masters Thesis, Bowling Green State University. Accessed January 27, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1371083757.

MLA Handbook (7th Edition):

Karabaeva, Kanykey E. “Photochemistry of Masked Pyrene-4,5-Dione.” 2013. Web. 27 Jan 2021.

Vancouver:

Karabaeva KE. Photochemistry of Masked Pyrene-4,5-Dione. [Internet] [Masters thesis]. Bowling Green State University; 2013. [cited 2021 Jan 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1371083757.

Council of Science Editors:

Karabaeva KE. Photochemistry of Masked Pyrene-4,5-Dione. [Masters Thesis]. Bowling Green State University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1371083757


Oregon State University

9. Aponso, G. Lalith M. Prenylated flavonoids from hops (Humulus lupulus) as monofunctional inducers of the carcinogen-detoxifying enzyme, NAD(P)H:quinone oxidoreductase.

Degree: MS, Toxicology, 1999, Oregon State University

Subjects/Keywords: Quinone

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APA (6th Edition):

Aponso, G. L. M. (1999). Prenylated flavonoids from hops (Humulus lupulus) as monofunctional inducers of the carcinogen-detoxifying enzyme, NAD(P)H:quinone oxidoreductase. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/33436

Chicago Manual of Style (16th Edition):

Aponso, G Lalith M. “Prenylated flavonoids from hops (Humulus lupulus) as monofunctional inducers of the carcinogen-detoxifying enzyme, NAD(P)H:quinone oxidoreductase.” 1999. Masters Thesis, Oregon State University. Accessed January 27, 2021. http://hdl.handle.net/1957/33436.

MLA Handbook (7th Edition):

Aponso, G Lalith M. “Prenylated flavonoids from hops (Humulus lupulus) as monofunctional inducers of the carcinogen-detoxifying enzyme, NAD(P)H:quinone oxidoreductase.” 1999. Web. 27 Jan 2021.

Vancouver:

Aponso GLM. Prenylated flavonoids from hops (Humulus lupulus) as monofunctional inducers of the carcinogen-detoxifying enzyme, NAD(P)H:quinone oxidoreductase. [Internet] [Masters thesis]. Oregon State University; 1999. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1957/33436.

Council of Science Editors:

Aponso GLM. Prenylated flavonoids from hops (Humulus lupulus) as monofunctional inducers of the carcinogen-detoxifying enzyme, NAD(P)H:quinone oxidoreductase. [Masters Thesis]. Oregon State University; 1999. Available from: http://hdl.handle.net/1957/33436


Michigan State University

10. Suggs, William Terry, 1945-. Part I: approaches to the synthesis of 2-paranitrophenyl-4,6-di-para-methoxyphenyl-benzene-1,3-quinone. Part II: the crystal structure of 2,4-di-para-methoxyphenyl-cyclobutadiene-1,3-quinone.

Degree: PhD, Department of Chemistry, 1973, Michigan State University

Subjects/Keywords: Quinone

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APA (6th Edition):

Suggs, William Terry, 1. (1973). Part I: approaches to the synthesis of 2-paranitrophenyl-4,6-di-para-methoxyphenyl-benzene-1,3-quinone. Part II: the crystal structure of 2,4-di-para-methoxyphenyl-cyclobutadiene-1,3-quinone. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:35969

Chicago Manual of Style (16th Edition):

Suggs, William Terry, 1945-. “Part I: approaches to the synthesis of 2-paranitrophenyl-4,6-di-para-methoxyphenyl-benzene-1,3-quinone. Part II: the crystal structure of 2,4-di-para-methoxyphenyl-cyclobutadiene-1,3-quinone.” 1973. Doctoral Dissertation, Michigan State University. Accessed January 27, 2021. http://etd.lib.msu.edu/islandora/object/etd:35969.

MLA Handbook (7th Edition):

Suggs, William Terry, 1945-. “Part I: approaches to the synthesis of 2-paranitrophenyl-4,6-di-para-methoxyphenyl-benzene-1,3-quinone. Part II: the crystal structure of 2,4-di-para-methoxyphenyl-cyclobutadiene-1,3-quinone.” 1973. Web. 27 Jan 2021.

Vancouver:

Suggs, William Terry 1. Part I: approaches to the synthesis of 2-paranitrophenyl-4,6-di-para-methoxyphenyl-benzene-1,3-quinone. Part II: the crystal structure of 2,4-di-para-methoxyphenyl-cyclobutadiene-1,3-quinone. [Internet] [Doctoral dissertation]. Michigan State University; 1973. [cited 2021 Jan 27]. Available from: http://etd.lib.msu.edu/islandora/object/etd:35969.

Council of Science Editors:

Suggs, William Terry 1. Part I: approaches to the synthesis of 2-paranitrophenyl-4,6-di-para-methoxyphenyl-benzene-1,3-quinone. Part II: the crystal structure of 2,4-di-para-methoxyphenyl-cyclobutadiene-1,3-quinone. [Doctoral Dissertation]. Michigan State University; 1973. Available from: http://etd.lib.msu.edu/islandora/object/etd:35969


Texas Christian University

11. Sun, Duoli. Synthesis and properties of quinone derivatives / by Duoli Sun.

Degree: 1997, Texas Christian University

Subjects/Keywords: Quinone

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APA (6th Edition):

Sun, D. (1997). Synthesis and properties of quinone derivatives / by Duoli Sun. (Thesis). Texas Christian University. Retrieved from https://repository.tcu.edu/handle/116099117/31825

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sun, Duoli. “Synthesis and properties of quinone derivatives / by Duoli Sun.” 1997. Thesis, Texas Christian University. Accessed January 27, 2021. https://repository.tcu.edu/handle/116099117/31825.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sun, Duoli. “Synthesis and properties of quinone derivatives / by Duoli Sun.” 1997. Web. 27 Jan 2021.

Vancouver:

Sun D. Synthesis and properties of quinone derivatives / by Duoli Sun. [Internet] [Thesis]. Texas Christian University; 1997. [cited 2021 Jan 27]. Available from: https://repository.tcu.edu/handle/116099117/31825.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sun D. Synthesis and properties of quinone derivatives / by Duoli Sun. [Thesis]. Texas Christian University; 1997. Available from: https://repository.tcu.edu/handle/116099117/31825

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Michigan State University

12. Watson, William David. Approaches to the synthesis of 2-(4-nitrophenyl)-4,6-di(4-methoxyphenol)benzene-1,3-quinone.

Degree: MS, Dept. of Chemistry, 1973, Michigan State University

Subjects/Keywords: Quinone

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APA (6th Edition):

Watson, W. D. (1973). Approaches to the synthesis of 2-(4-nitrophenyl)-4,6-di(4-methoxyphenol)benzene-1,3-quinone. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:13769

Chicago Manual of Style (16th Edition):

Watson, William David. “Approaches to the synthesis of 2-(4-nitrophenyl)-4,6-di(4-methoxyphenol)benzene-1,3-quinone.” 1973. Masters Thesis, Michigan State University. Accessed January 27, 2021. http://etd.lib.msu.edu/islandora/object/etd:13769.

MLA Handbook (7th Edition):

Watson, William David. “Approaches to the synthesis of 2-(4-nitrophenyl)-4,6-di(4-methoxyphenol)benzene-1,3-quinone.” 1973. Web. 27 Jan 2021.

Vancouver:

Watson WD. Approaches to the synthesis of 2-(4-nitrophenyl)-4,6-di(4-methoxyphenol)benzene-1,3-quinone. [Internet] [Masters thesis]. Michigan State University; 1973. [cited 2021 Jan 27]. Available from: http://etd.lib.msu.edu/islandora/object/etd:13769.

Council of Science Editors:

Watson WD. Approaches to the synthesis of 2-(4-nitrophenyl)-4,6-di(4-methoxyphenol)benzene-1,3-quinone. [Masters Thesis]. Michigan State University; 1973. Available from: http://etd.lib.msu.edu/islandora/object/etd:13769


Portland State University

13. Mbiya, Wilbes. Substituent Effects on Reactivity and Allergenicity of Benzoquinone.

Degree: PhD, Chemistry, 2013, Portland State University

  Benzoquinone (BQ) is an extremely potent electrophilic contact allergen that haptenates endogenous proteins through Michael addition (MA). It is also hypothesized that BQ may… (more)

Subjects/Keywords: Quinone  – Reactivity; Quinone  – Allergenicity; Protein binding; Chemistry

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APA (6th Edition):

Mbiya, W. (2013). Substituent Effects on Reactivity and Allergenicity of Benzoquinone. (Doctoral Dissertation). Portland State University. Retrieved from https://pdxscholar.library.pdx.edu/open_access_etds/1406

Chicago Manual of Style (16th Edition):

Mbiya, Wilbes. “Substituent Effects on Reactivity and Allergenicity of Benzoquinone.” 2013. Doctoral Dissertation, Portland State University. Accessed January 27, 2021. https://pdxscholar.library.pdx.edu/open_access_etds/1406.

MLA Handbook (7th Edition):

Mbiya, Wilbes. “Substituent Effects on Reactivity and Allergenicity of Benzoquinone.” 2013. Web. 27 Jan 2021.

Vancouver:

Mbiya W. Substituent Effects on Reactivity and Allergenicity of Benzoquinone. [Internet] [Doctoral dissertation]. Portland State University; 2013. [cited 2021 Jan 27]. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/1406.

Council of Science Editors:

Mbiya W. Substituent Effects on Reactivity and Allergenicity of Benzoquinone. [Doctoral Dissertation]. Portland State University; 2013. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/1406


Nelson Mandela Metropolitan University

14. Taljaard, Jana Heloïse. Synthesis, properties and reactions of Novel Quinone Methides.

Degree: PhD, Faculty of Science, 2007, Nelson Mandela Metropolitan University

 Novel p-quinone methides have been synthesized by the dealkylation of 5-(p-alkyloxyaryl)- 10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ols and related compounds. Aspects of the dealkylation reaction were investigated using computational methods… (more)

Subjects/Keywords: Quinone; Chemistry, Organic

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APA (6th Edition):

Taljaard, J. H. (2007). Synthesis, properties and reactions of Novel Quinone Methides. (Doctoral Dissertation). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/616

Chicago Manual of Style (16th Edition):

Taljaard, Jana Heloïse. “Synthesis, properties and reactions of Novel Quinone Methides.” 2007. Doctoral Dissertation, Nelson Mandela Metropolitan University. Accessed January 27, 2021. http://hdl.handle.net/10948/616.

MLA Handbook (7th Edition):

Taljaard, Jana Heloïse. “Synthesis, properties and reactions of Novel Quinone Methides.” 2007. Web. 27 Jan 2021.

Vancouver:

Taljaard JH. Synthesis, properties and reactions of Novel Quinone Methides. [Internet] [Doctoral dissertation]. Nelson Mandela Metropolitan University; 2007. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10948/616.

Council of Science Editors:

Taljaard JH. Synthesis, properties and reactions of Novel Quinone Methides. [Doctoral Dissertation]. Nelson Mandela Metropolitan University; 2007. Available from: http://hdl.handle.net/10948/616


University of Manchester

15. Bogle, Katherine Mary. An Organocatalytic Oxidative Coupling Strategy for the Synthesis of Arylated Quaternary Stereocentres and its Application in the Total Synthesis of Powelline and Buphanidrine.

Degree: 2011, University of Manchester

 The synthesis of compounds containing α-arylated quaternary stereogenic centres is a significant synthetic challenge. This thesis describes the development of an organocatalytic methodology for the… (more)

Subjects/Keywords: ortho-benzoquinone; organocatalyst; powelline

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APA (6th Edition):

Bogle, K. M. (2011). An Organocatalytic Oxidative Coupling Strategy for the Synthesis of Arylated Quaternary Stereocentres and its Application in the Total Synthesis of Powelline and Buphanidrine. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:105971

Chicago Manual of Style (16th Edition):

Bogle, Katherine Mary. “An Organocatalytic Oxidative Coupling Strategy for the Synthesis of Arylated Quaternary Stereocentres and its Application in the Total Synthesis of Powelline and Buphanidrine.” 2011. Doctoral Dissertation, University of Manchester. Accessed January 27, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:105971.

MLA Handbook (7th Edition):

Bogle, Katherine Mary. “An Organocatalytic Oxidative Coupling Strategy for the Synthesis of Arylated Quaternary Stereocentres and its Application in the Total Synthesis of Powelline and Buphanidrine.” 2011. Web. 27 Jan 2021.

Vancouver:

Bogle KM. An Organocatalytic Oxidative Coupling Strategy for the Synthesis of Arylated Quaternary Stereocentres and its Application in the Total Synthesis of Powelline and Buphanidrine. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2021 Jan 27]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:105971.

Council of Science Editors:

Bogle KM. An Organocatalytic Oxidative Coupling Strategy for the Synthesis of Arylated Quaternary Stereocentres and its Application in the Total Synthesis of Powelline and Buphanidrine. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:105971


University of Manchester

16. Bogle, Katherine Mary. An organocatalytic oxidative coupling strategy for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine.

Degree: PhD, 2011, University of Manchester

 The synthesis of compounds containing α-arylated quaternary stereogenic centres is a significant synthetic challenge. This thesis describes the development of an organocatalytic methodology for the… (more)

Subjects/Keywords: 547.7; ortho-benzoquinone; organocatalyst; powelline

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APA (6th Edition):

Bogle, K. M. (2011). An organocatalytic oxidative coupling strategy for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/an-organocatalytic-oxidative-coupling-strategy-for-the-synthesis-of-arylated-quaternary-stereocentres-and-its-application-in-the-total-synthesis-of-powelline-and-buphanidrine(4038d899-f157-4ac5-904b-128553be92ff).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528502

Chicago Manual of Style (16th Edition):

Bogle, Katherine Mary. “An organocatalytic oxidative coupling strategy for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine.” 2011. Doctoral Dissertation, University of Manchester. Accessed January 27, 2021. https://www.research.manchester.ac.uk/portal/en/theses/an-organocatalytic-oxidative-coupling-strategy-for-the-synthesis-of-arylated-quaternary-stereocentres-and-its-application-in-the-total-synthesis-of-powelline-and-buphanidrine(4038d899-f157-4ac5-904b-128553be92ff).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528502.

MLA Handbook (7th Edition):

Bogle, Katherine Mary. “An organocatalytic oxidative coupling strategy for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine.” 2011. Web. 27 Jan 2021.

Vancouver:

Bogle KM. An organocatalytic oxidative coupling strategy for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2021 Jan 27]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/an-organocatalytic-oxidative-coupling-strategy-for-the-synthesis-of-arylated-quaternary-stereocentres-and-its-application-in-the-total-synthesis-of-powelline-and-buphanidrine(4038d899-f157-4ac5-904b-128553be92ff).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528502.

Council of Science Editors:

Bogle KM. An organocatalytic oxidative coupling strategy for the synthesis of arylated quaternary stereocentres and its application in the total synthesis of powelline and buphanidrine. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/an-organocatalytic-oxidative-coupling-strategy-for-the-synthesis-of-arylated-quaternary-stereocentres-and-its-application-in-the-total-synthesis-of-powelline-and-buphanidrine(4038d899-f157-4ac5-904b-128553be92ff).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528502

17. Moitessier, Clémence. Élaboration de dérivés d'ortho-phtalaldéhyde et de nanomatériaux de type Quantum Dots en vue de l'amélioration de l'analyse fluorimétrique des amines biogènes : Development of artho-phtalaldehyde derivatives and Qauntum Dots type nanomaterials in order to improve the biogenic amines fluorimetric analysis.

Degree: Docteur es, Chimie. Chimie organique, 2019, Littoral

Les amines biogènes (AB) sont des substances physiologiquement actives résultant de la décarboxylation enzymatique des acides aminés libres. Elles participent, dans le corps, aux processus… (more)

Subjects/Keywords: Histamine; Quantum Dots; Ortho-phtalaldéhyde; Histamine; Quantum Dots; Ortho-phtalaldehyde

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APA (6th Edition):

Moitessier, C. (2019). Élaboration de dérivés d'ortho-phtalaldéhyde et de nanomatériaux de type Quantum Dots en vue de l'amélioration de l'analyse fluorimétrique des amines biogènes : Development of artho-phtalaldehyde derivatives and Qauntum Dots type nanomaterials in order to improve the biogenic amines fluorimetric analysis. (Doctoral Dissertation). Littoral. Retrieved from http://www.theses.fr/2019DUNK0523

Chicago Manual of Style (16th Edition):

Moitessier, Clémence. “Élaboration de dérivés d'ortho-phtalaldéhyde et de nanomatériaux de type Quantum Dots en vue de l'amélioration de l'analyse fluorimétrique des amines biogènes : Development of artho-phtalaldehyde derivatives and Qauntum Dots type nanomaterials in order to improve the biogenic amines fluorimetric analysis.” 2019. Doctoral Dissertation, Littoral. Accessed January 27, 2021. http://www.theses.fr/2019DUNK0523.

MLA Handbook (7th Edition):

Moitessier, Clémence. “Élaboration de dérivés d'ortho-phtalaldéhyde et de nanomatériaux de type Quantum Dots en vue de l'amélioration de l'analyse fluorimétrique des amines biogènes : Development of artho-phtalaldehyde derivatives and Qauntum Dots type nanomaterials in order to improve the biogenic amines fluorimetric analysis.” 2019. Web. 27 Jan 2021.

Vancouver:

Moitessier C. Élaboration de dérivés d'ortho-phtalaldéhyde et de nanomatériaux de type Quantum Dots en vue de l'amélioration de l'analyse fluorimétrique des amines biogènes : Development of artho-phtalaldehyde derivatives and Qauntum Dots type nanomaterials in order to improve the biogenic amines fluorimetric analysis. [Internet] [Doctoral dissertation]. Littoral; 2019. [cited 2021 Jan 27]. Available from: http://www.theses.fr/2019DUNK0523.

Council of Science Editors:

Moitessier C. Élaboration de dérivés d'ortho-phtalaldéhyde et de nanomatériaux de type Quantum Dots en vue de l'amélioration de l'analyse fluorimétrique des amines biogènes : Development of artho-phtalaldehyde derivatives and Qauntum Dots type nanomaterials in order to improve the biogenic amines fluorimetric analysis. [Doctoral Dissertation]. Littoral; 2019. Available from: http://www.theses.fr/2019DUNK0523


Penn State University

18. Gorka, Michael J. Electron Extraction from the A1a and A1b sites of Photosystem I.

Degree: 2015, Penn State University

 This dissertation describes an analysis of the kinetic properties of cyanobacterial Photosystem I (PS I) and how the principles learned can be applied for the… (more)

Subjects/Keywords: Photosystem I; Dihydrogen; Quinone

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APA (6th Edition):

Gorka, M. J. (2015). Electron Extraction from the A1a and A1b sites of Photosystem I. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/27309

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gorka, Michael J. “Electron Extraction from the A1a and A1b sites of Photosystem I.” 2015. Thesis, Penn State University. Accessed January 27, 2021. https://submit-etda.libraries.psu.edu/catalog/27309.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gorka, Michael J. “Electron Extraction from the A1a and A1b sites of Photosystem I.” 2015. Web. 27 Jan 2021.

Vancouver:

Gorka MJ. Electron Extraction from the A1a and A1b sites of Photosystem I. [Internet] [Thesis]. Penn State University; 2015. [cited 2021 Jan 27]. Available from: https://submit-etda.libraries.psu.edu/catalog/27309.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gorka MJ. Electron Extraction from the A1a and A1b sites of Photosystem I. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/27309

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Johannesburg

19. Siemens, Hester. Oksidasie van suikers en aromatiese verbindings met dimetieldioksiraan.

Degree: 2014, University of Johannesburg

M.Sc. (Chemistry)

The aim of this study was to investigate the oxidation of aromatic compounds and benzylidene acetals with dimethyldioxinne. Dimethyldioxirane, either by Insitu preparation… (more)

Subjects/Keywords: Aromatic compounds; Sugars; Oxidation; Quinone

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APA (6th Edition):

Siemens, H. (2014). Oksidasie van suikers en aromatiese verbindings met dimetieldioksiraan. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/10195

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Siemens, Hester. “Oksidasie van suikers en aromatiese verbindings met dimetieldioksiraan.” 2014. Thesis, University of Johannesburg. Accessed January 27, 2021. http://hdl.handle.net/10210/10195.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Siemens, Hester. “Oksidasie van suikers en aromatiese verbindings met dimetieldioksiraan.” 2014. Web. 27 Jan 2021.

Vancouver:

Siemens H. Oksidasie van suikers en aromatiese verbindings met dimetieldioksiraan. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10210/10195.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Siemens H. Oksidasie van suikers en aromatiese verbindings met dimetieldioksiraan. [Thesis]. University of Johannesburg; 2014. Available from: http://hdl.handle.net/10210/10195

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Houston

20. -5669-4609. Design, Synthesis, and Characterization of Quinone Electrode Materials for Sustainable Energy Storage.

Degree: PhD, Materials Engineering, 2017, University of Houston

 The energy crisis and environmental issues have instigated the integration of renewable energy sources into the electric grid. A robust, safe, and long-life energy storage… (more)

Subjects/Keywords: Quinone; Battery; Mechanism; Electrochemistry

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APA (6th Edition):

-5669-4609. (2017). Design, Synthesis, and Characterization of Quinone Electrode Materials for Sustainable Energy Storage. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/4818

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-5669-4609. “Design, Synthesis, and Characterization of Quinone Electrode Materials for Sustainable Energy Storage.” 2017. Doctoral Dissertation, University of Houston. Accessed January 27, 2021. http://hdl.handle.net/10657/4818.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-5669-4609. “Design, Synthesis, and Characterization of Quinone Electrode Materials for Sustainable Energy Storage.” 2017. Web. 27 Jan 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-5669-4609. Design, Synthesis, and Characterization of Quinone Electrode Materials for Sustainable Energy Storage. [Internet] [Doctoral dissertation]. University of Houston; 2017. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10657/4818.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-5669-4609. Design, Synthesis, and Characterization of Quinone Electrode Materials for Sustainable Energy Storage. [Doctoral Dissertation]. University of Houston; 2017. Available from: http://hdl.handle.net/10657/4818

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


East Carolina University

21. Duffy, Brian. Solvent and Solubility Effects on Quinone Ratios.

Degree: 2012, East Carolina University

 Monoquinones and diquinones are a biologically and chemically important class of compounds that can be found in numerous natural products such as: thymoquinone oosporein coenzyme… (more)

Subjects/Keywords: Quinone – Synthesis – Research; Synthetic products

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APA (6th Edition):

Duffy, B. (2012). Solvent and Solubility Effects on Quinone Ratios. (Masters Thesis). East Carolina University. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14564

Chicago Manual of Style (16th Edition):

Duffy, Brian. “Solvent and Solubility Effects on Quinone Ratios.” 2012. Masters Thesis, East Carolina University. Accessed January 27, 2021. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14564.

MLA Handbook (7th Edition):

Duffy, Brian. “Solvent and Solubility Effects on Quinone Ratios.” 2012. Web. 27 Jan 2021.

Vancouver:

Duffy B. Solvent and Solubility Effects on Quinone Ratios. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2021 Jan 27]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14564.

Council of Science Editors:

Duffy B. Solvent and Solubility Effects on Quinone Ratios. [Masters Thesis]. East Carolina University; 2012. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14564


University of Kansas

22. Haugeberg, Benjamin John. Development and Application of Quinone-Catalyzed C-C Bond Cleavage.

Degree: MS, Chemistry, 2016, University of Kansas

 Organocatalysis is a synthetic field of ever increasing development and utility. Of the reactions and small molecule catalysts developed over the last 20 years, a… (more)

Subjects/Keywords: Chemistry; Homologation; Organocatalysis; Quinone

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APA (6th Edition):

Haugeberg, B. J. (2016). Development and Application of Quinone-Catalyzed C-C Bond Cleavage. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/25765

Chicago Manual of Style (16th Edition):

Haugeberg, Benjamin John. “Development and Application of Quinone-Catalyzed C-C Bond Cleavage.” 2016. Masters Thesis, University of Kansas. Accessed January 27, 2021. http://hdl.handle.net/1808/25765.

MLA Handbook (7th Edition):

Haugeberg, Benjamin John. “Development and Application of Quinone-Catalyzed C-C Bond Cleavage.” 2016. Web. 27 Jan 2021.

Vancouver:

Haugeberg BJ. Development and Application of Quinone-Catalyzed C-C Bond Cleavage. [Internet] [Masters thesis]. University of Kansas; 2016. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/1808/25765.

Council of Science Editors:

Haugeberg BJ. Development and Application of Quinone-Catalyzed C-C Bond Cleavage. [Masters Thesis]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/25765


University of British Columbia

23. Wat, Chi-Kit. Biosynthetic studies on the p-benzoquinones produced by Shanorella Spirotricha Benjamin.

Degree: PhD, Botany, 1969, University of British Columbia

 From the culture medium of Shanorella spirotricha Benjamin, four p-benzoquinones have been isolated and identified. The major pigment is shanorellin (2,6-dimethyl-3-hydroxymethyl-5-hydroxy-1,4-benzoquinone). The other three pigments… (more)

Subjects/Keywords: Quinone; Quinones

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APA (6th Edition):

Wat, C. (1969). Biosynthetic studies on the p-benzoquinones produced by Shanorella Spirotricha Benjamin. (Doctoral Dissertation). University of British Columbia. Retrieved from http://hdl.handle.net/2429/35041

Chicago Manual of Style (16th Edition):

Wat, Chi-Kit. “Biosynthetic studies on the p-benzoquinones produced by Shanorella Spirotricha Benjamin.” 1969. Doctoral Dissertation, University of British Columbia. Accessed January 27, 2021. http://hdl.handle.net/2429/35041.

MLA Handbook (7th Edition):

Wat, Chi-Kit. “Biosynthetic studies on the p-benzoquinones produced by Shanorella Spirotricha Benjamin.” 1969. Web. 27 Jan 2021.

Vancouver:

Wat C. Biosynthetic studies on the p-benzoquinones produced by Shanorella Spirotricha Benjamin. [Internet] [Doctoral dissertation]. University of British Columbia; 1969. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/2429/35041.

Council of Science Editors:

Wat C. Biosynthetic studies on the p-benzoquinones produced by Shanorella Spirotricha Benjamin. [Doctoral Dissertation]. University of British Columbia; 1969. Available from: http://hdl.handle.net/2429/35041


The Ohio State University

24. Chenard, Bertrand L. Synthesis via protected quinones.

Degree: PhD, Graduate School, 1981, The Ohio State University

Subjects/Keywords: Chemistry; Quinone

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APA (6th Edition):

Chenard, B. L. (1981). Synthesis via protected quinones. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487156696794053

Chicago Manual of Style (16th Edition):

Chenard, Bertrand L. “Synthesis via protected quinones.” 1981. Doctoral Dissertation, The Ohio State University. Accessed January 27, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487156696794053.

MLA Handbook (7th Edition):

Chenard, Bertrand L. “Synthesis via protected quinones.” 1981. Web. 27 Jan 2021.

Vancouver:

Chenard BL. Synthesis via protected quinones. [Internet] [Doctoral dissertation]. The Ohio State University; 1981. [cited 2021 Jan 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487156696794053.

Council of Science Editors:

Chenard BL. Synthesis via protected quinones. [Doctoral Dissertation]. The Ohio State University; 1981. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487156696794053


The Ohio State University

25. Manning, Michael John. The synthesis and chemistry of quinone mono- and bisketals .

Degree: PhD, Graduate School, 1977, The Ohio State University

Subjects/Keywords: Chemistry; Quinone

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APA (6th Edition):

Manning, M. J. (1977). The synthesis and chemistry of quinone mono- and bisketals . (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487005965829607

Chicago Manual of Style (16th Edition):

Manning, Michael John. “The synthesis and chemistry of quinone mono- and bisketals .” 1977. Doctoral Dissertation, The Ohio State University. Accessed January 27, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487005965829607.

MLA Handbook (7th Edition):

Manning, Michael John. “The synthesis and chemistry of quinone mono- and bisketals .” 1977. Web. 27 Jan 2021.

Vancouver:

Manning MJ. The synthesis and chemistry of quinone mono- and bisketals . [Internet] [Doctoral dissertation]. The Ohio State University; 1977. [cited 2021 Jan 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487005965829607.

Council of Science Editors:

Manning MJ. The synthesis and chemistry of quinone mono- and bisketals . [Doctoral Dissertation]. The Ohio State University; 1977. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487005965829607


The Ohio State University

26. Davis, Charles Cavender. The synthesis of 9,10-dimethyl-1,2-benz-3,4-anthraquinone .

Degree: PhD, Graduate School, 1966, The Ohio State University

Subjects/Keywords: Chemistry; Quinone

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APA (6th Edition):

Davis, C. C. (1966). The synthesis of 9,10-dimethyl-1,2-benz-3,4-anthraquinone . (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1486633544273165

Chicago Manual of Style (16th Edition):

Davis, Charles Cavender. “The synthesis of 9,10-dimethyl-1,2-benz-3,4-anthraquinone .” 1966. Doctoral Dissertation, The Ohio State University. Accessed January 27, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486633544273165.

MLA Handbook (7th Edition):

Davis, Charles Cavender. “The synthesis of 9,10-dimethyl-1,2-benz-3,4-anthraquinone .” 1966. Web. 27 Jan 2021.

Vancouver:

Davis CC. The synthesis of 9,10-dimethyl-1,2-benz-3,4-anthraquinone . [Internet] [Doctoral dissertation]. The Ohio State University; 1966. [cited 2021 Jan 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486633544273165.

Council of Science Editors:

Davis CC. The synthesis of 9,10-dimethyl-1,2-benz-3,4-anthraquinone . [Doctoral Dissertation]. The Ohio State University; 1966. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486633544273165


NSYSU

27. Peng, Jheng-syong. (ä¸) Pyrolytic and Photolytic Studies of 2-(Dimethylamino)styrylarenes and 2-(Benzylmethylamino)styrylarenes (äº) Pyrolytic Study of Benzoic 1,3-Dimethyl-2-indolyl Anhydride.

Degree: Master, Chemistry, 2009, NSYSU

 ä¸.Pyrolysis of 2-(N,N-dimethylamino)styrylarenes (29a-e) and 2-(N,N- benzylmethylamino)styrylarenes (30a-f) both gave 2-(ar-2-yl)- benzo[b]arenes 35a-f, 39a-e, their isomers 36a-e, 40a-e and the other products. On the other… (more)

Subjects/Keywords: flash vacuum pyrolysis; stilbene; photolysis; ortho-methyleneketene

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APA (6th Edition):

Peng, J. (2009). (ä¸) Pyrolytic and Photolytic Studies of 2-(Dimethylamino)styrylarenes and 2-(Benzylmethylamino)styrylarenes (äº) Pyrolytic Study of Benzoic 1,3-Dimethyl-2-indolyl Anhydride. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0727109-182032

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Peng, Jheng-syong. “(ä¸) Pyrolytic and Photolytic Studies of 2-(Dimethylamino)styrylarenes and 2-(Benzylmethylamino)styrylarenes (äº) Pyrolytic Study of Benzoic 1,3-Dimethyl-2-indolyl Anhydride.” 2009. Thesis, NSYSU. Accessed January 27, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0727109-182032.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Peng, Jheng-syong. “(ä¸) Pyrolytic and Photolytic Studies of 2-(Dimethylamino)styrylarenes and 2-(Benzylmethylamino)styrylarenes (äº) Pyrolytic Study of Benzoic 1,3-Dimethyl-2-indolyl Anhydride.” 2009. Web. 27 Jan 2021.

Vancouver:

Peng J. (ä¸) Pyrolytic and Photolytic Studies of 2-(Dimethylamino)styrylarenes and 2-(Benzylmethylamino)styrylarenes (äº) Pyrolytic Study of Benzoic 1,3-Dimethyl-2-indolyl Anhydride. [Internet] [Thesis]. NSYSU; 2009. [cited 2021 Jan 27]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0727109-182032.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Peng J. (ä¸) Pyrolytic and Photolytic Studies of 2-(Dimethylamino)styrylarenes and 2-(Benzylmethylamino)styrylarenes (äº) Pyrolytic Study of Benzoic 1,3-Dimethyl-2-indolyl Anhydride. [Thesis]. NSYSU; 2009. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0727109-182032

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

28. Pandya,Piyosh K. Ortho hydroxy ketoximes as analytical reagents;.

Degree: Chemistry, 2015, Gujarat University

Abstract Not Available

Data not available

Advisors/Committee Members: Thakor,V M.

Subjects/Keywords: Hydroxy; Ortho; Reagents

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APA (6th Edition):

K, P. (2015). Ortho hydroxy ketoximes as analytical reagents;. (Thesis). Gujarat University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/47683

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

K, Pandya,Piyosh. “Ortho hydroxy ketoximes as analytical reagents;.” 2015. Thesis, Gujarat University. Accessed January 27, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/47683.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

K, Pandya,Piyosh. “Ortho hydroxy ketoximes as analytical reagents;.” 2015. Web. 27 Jan 2021.

Vancouver:

K P. Ortho hydroxy ketoximes as analytical reagents;. [Internet] [Thesis]. Gujarat University; 2015. [cited 2021 Jan 27]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/47683.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

K P. Ortho hydroxy ketoximes as analytical reagents;. [Thesis]. Gujarat University; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/47683

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Georgia

29. Palekar, Leena Dhairyahsil. Anaerobic microbial dechlorination of polychlorinated biphenyls.

Degree: 2014, University of Georgia

 The LCP Superfund site in Brunswick, Georgia, was extensively contaminated with Aroclor 1268, a mixture of highly chlorinated polychlorinated biphenyl (PCB) congeners. This study investigates… (more)

Subjects/Keywords: polychlorinated biphenyls; dechlorination; Aroclor 1268; ortho dechlorination

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APA (6th Edition):

Palekar, L. D. (2014). Anaerobic microbial dechlorination of polychlorinated biphenyls. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/29280

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Palekar, Leena Dhairyahsil. “Anaerobic microbial dechlorination of polychlorinated biphenyls.” 2014. Thesis, University of Georgia. Accessed January 27, 2021. http://hdl.handle.net/10724/29280.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Palekar, Leena Dhairyahsil. “Anaerobic microbial dechlorination of polychlorinated biphenyls.” 2014. Web. 27 Jan 2021.

Vancouver:

Palekar LD. Anaerobic microbial dechlorination of polychlorinated biphenyls. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 27]. Available from: http://hdl.handle.net/10724/29280.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Palekar LD. Anaerobic microbial dechlorination of polychlorinated biphenyls. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/29280

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Miami University

30. Chu, Meng. Intermolecular Association of an Oblong Shape-persistent Macrocycle and Refunctionalization of Folding ortho-Phenylene Oligomers.

Degree: PhD, Chemistry, 2016, Miami University

 This dissertation contains two main parts. The first part presents the synthesis, characterization, and aggregation properties of new tetrabenzo[18]cyclyne(TBCs) macrocycles. The second part is focused… (more)

Subjects/Keywords: Organic Chemistry; intermolecular association, macrocycle, ortho-Phenylene

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Chu, M. (2016). Intermolecular Association of an Oblong Shape-persistent Macrocycle and Refunctionalization of Folding ortho-Phenylene Oligomers. (Doctoral Dissertation). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1468959764

Chicago Manual of Style (16th Edition):

Chu, Meng. “Intermolecular Association of an Oblong Shape-persistent Macrocycle and Refunctionalization of Folding ortho-Phenylene Oligomers.” 2016. Doctoral Dissertation, Miami University. Accessed January 27, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=miami1468959764.

MLA Handbook (7th Edition):

Chu, Meng. “Intermolecular Association of an Oblong Shape-persistent Macrocycle and Refunctionalization of Folding ortho-Phenylene Oligomers.” 2016. Web. 27 Jan 2021.

Vancouver:

Chu M. Intermolecular Association of an Oblong Shape-persistent Macrocycle and Refunctionalization of Folding ortho-Phenylene Oligomers. [Internet] [Doctoral dissertation]. Miami University; 2016. [cited 2021 Jan 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1468959764.

Council of Science Editors:

Chu M. Intermolecular Association of an Oblong Shape-persistent Macrocycle and Refunctionalization of Folding ortho-Phenylene Oligomers. [Doctoral Dissertation]. Miami University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1468959764

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