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You searched for subject:(Indoles). Showing records 1 – 30 of 66 total matches.

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University of New South Wales

1. Kandemir, Hakan. Synthesis of novel BIS-indole systems.

Degree: Chemistry, 2011, University of New South Wales

 The primary aim of this project was to synthesize novel 2,2′- and 7,7′-linked bis-indole systems from methoxy activated indoles, and investigate their ability to undergo… (more)

Subjects/Keywords: Oxotryptamines; Indoles; BIS-indoles; Oxadiazoles

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APA (6th Edition):

Kandemir, H. (2011). Synthesis of novel BIS-indole systems. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51542 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10229/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Kandemir, Hakan. “Synthesis of novel BIS-indole systems.” 2011. Doctoral Dissertation, University of New South Wales. Accessed December 08, 2019. http://handle.unsw.edu.au/1959.4/51542 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10229/SOURCE02?view=true.

MLA Handbook (7th Edition):

Kandemir, Hakan. “Synthesis of novel BIS-indole systems.” 2011. Web. 08 Dec 2019.

Vancouver:

Kandemir H. Synthesis of novel BIS-indole systems. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2019 Dec 08]. Available from: http://handle.unsw.edu.au/1959.4/51542 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10229/SOURCE02?view=true.

Council of Science Editors:

Kandemir H. Synthesis of novel BIS-indole systems. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51542 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10229/SOURCE02?view=true

2. Gorja, Dhilli Rao. Synthesis and In Vitro Pharmacological Evaluation of Indoles and Alkynyl substituted Thieno Pyrimidines, Indazoles and Pyrazoles; -.

Degree: Chemistry, 2013, Jawaharlal Nehru Technological University, Hyderabad

Investigations embodied in this thesis entitled Synthesis and In vitro newlinePharmacological Evaluation of Indoles and Alkynyl Substituted Thieno pyrimidines, Indazoles and Pyrazoles have been presented… (more)

Subjects/Keywords: Evaluation; Indoles; Pharmacological; Pyrazoles; Synthesis

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APA (6th Edition):

Gorja, D. R. (2013). Synthesis and In Vitro Pharmacological Evaluation of Indoles and Alkynyl substituted Thieno Pyrimidines, Indazoles and Pyrazoles; -. (Thesis). Jawaharlal Nehru Technological University, Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19377

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):

Gorja, Dhilli Rao. “Synthesis and In Vitro Pharmacological Evaluation of Indoles and Alkynyl substituted Thieno Pyrimidines, Indazoles and Pyrazoles; -.” 2013. Thesis, Jawaharlal Nehru Technological University, Hyderabad. Accessed December 08, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/19377.

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

MLA Handbook (7th Edition):

Gorja, Dhilli Rao. “Synthesis and In Vitro Pharmacological Evaluation of Indoles and Alkynyl substituted Thieno Pyrimidines, Indazoles and Pyrazoles; -.” 2013. Web. 08 Dec 2019.

Vancouver:

Gorja DR. Synthesis and In Vitro Pharmacological Evaluation of Indoles and Alkynyl substituted Thieno Pyrimidines, Indazoles and Pyrazoles; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. [cited 2019 Dec 08]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19377.

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

Council of Science Editors:

Gorja DR. Synthesis and In Vitro Pharmacological Evaluation of Indoles and Alkynyl substituted Thieno Pyrimidines, Indazoles and Pyrazoles; -. [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19377

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

3. Hammoud, Sokaina. Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization.

Degree: Docteur es, Chimie organique, 2015, Université François-Rabelais de Tours

Une nouvelle voie d’accès à des structures tri-cycliques originaux les « oxazino-indole di-iodés» a été mise au point à partir des acides 1H-indole-2-carboxyliques commerciaux ou… (more)

Subjects/Keywords: Indoles; Isoindoles; Iodocyclisation; Cross-coupling; Indoles; Isoindoles; Iodocyclization; Cross-coupling

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APA (6th Edition):

Hammoud, S. (2015). Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2015TOUR4034

Chicago Manual of Style (16th Edition):

Hammoud, Sokaina. “Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization.” 2015. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed December 08, 2019. http://www.theses.fr/2015TOUR4034.

MLA Handbook (7th Edition):

Hammoud, Sokaina. “Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization.” 2015. Web. 08 Dec 2019.

Vancouver:

Hammoud S. Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2015. [cited 2019 Dec 08]. Available from: http://www.theses.fr/2015TOUR4034.

Council of Science Editors:

Hammoud S. Accès à de nouvelles structures tricycliques di-iodes à base indolique et isoindolique par iodocyclisation : Access to new di-iodinated tricyclic structures based on indoles and isoindoles by iodocyclization. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2015. Available from: http://www.theses.fr/2015TOUR4034


Iowa State University

4. Lakshminarayan, Ganeshkumar. Synthetic studies of diphenyl ether and anthraquinone natural products.

Degree: 2009, Iowa State University

 Organic chemistry is the most important branch of chemistry as it serves many aspects of human life. As the involvement of organic chemistry in our… (more)

Subjects/Keywords: indoles; littorachalcone; Methodology; rubianine; Synthesis; topopyrone; Chemistry

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APA (6th Edition):

Lakshminarayan, G. (2009). Synthetic studies of diphenyl ether and anthraquinone natural products. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/11163

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):

Lakshminarayan, Ganeshkumar. “Synthetic studies of diphenyl ether and anthraquinone natural products.” 2009. Thesis, Iowa State University. Accessed December 08, 2019. https://lib.dr.iastate.edu/etd/11163.

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

MLA Handbook (7th Edition):

Lakshminarayan, Ganeshkumar. “Synthetic studies of diphenyl ether and anthraquinone natural products.” 2009. Web. 08 Dec 2019.

Vancouver:

Lakshminarayan G. Synthetic studies of diphenyl ether and anthraquinone natural products. [Internet] [Thesis]. Iowa State University; 2009. [cited 2019 Dec 08]. Available from: https://lib.dr.iastate.edu/etd/11163.

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

Council of Science Editors:

Lakshminarayan G. Synthetic studies of diphenyl ether and anthraquinone natural products. [Thesis]. Iowa State University; 2009. Available from: https://lib.dr.iastate.edu/etd/11163

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


University of New South Wales

5. Khan, Taj Usman. Synthesis of new fused heterocyclic systems.

Degree: Chemistry, 2010, University of New South Wales

 The primary aim of this project was to synthesize novel 4,6-dihydroxyindoles and 5,7-dihydroxyquinolin-2-ones and to study their reactivity. 4,6-Dibenzyloxyindoles were synthesised from 3,5-dibenzyloxyaniline. The synthesis… (more)

Subjects/Keywords: Anti-cancer; Indoles; Quinolones; Anti-fungal; Furoindoles

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APA (6th Edition):

Khan, T. U. (2010). Synthesis of new fused heterocyclic systems. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50408 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9294/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Khan, Taj Usman. “Synthesis of new fused heterocyclic systems.” 2010. Doctoral Dissertation, University of New South Wales. Accessed December 08, 2019. http://handle.unsw.edu.au/1959.4/50408 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9294/SOURCE02?view=true.

MLA Handbook (7th Edition):

Khan, Taj Usman. “Synthesis of new fused heterocyclic systems.” 2010. Web. 08 Dec 2019.

Vancouver:

Khan TU. Synthesis of new fused heterocyclic systems. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Dec 08]. Available from: http://handle.unsw.edu.au/1959.4/50408 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9294/SOURCE02?view=true.

Council of Science Editors:

Khan TU. Synthesis of new fused heterocyclic systems. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/50408 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9294/SOURCE02?view=true

6. Chaabouni, Slim. Contribution à la chimie des cinnamates ortho-fonctionnalisés : Exploitation comme (1) précurseurs synthétiques d'hétérocycles, (2) antennes photoactivables de complexes d'ions lanthanides luminescents : Contribution to the chemistry of ortho-functionalized cinnamates : exploitation as (1) building blocks for heterocyclic synthesis, (2) photoactivatable sensitizers of luminescent lanthanide complexes.

Degree: Docteur es, Chimie organique, 2017, Université Toulouse III – Paul Sabatier

La chimie des cinnamates ortho-fonctionnalisés est particulièrement riche et variée, comme en témoigne le nombre important de méthodologies de synthèse reposant sur leur utilisation comme… (more)

Subjects/Keywords: Cinnamates; Coumarines; Indoles; Lanthanide; Photoactivation; Luminescence; Cinnamates; Coumarins; Indoles; Lanthanide; Photoactivation; Luminescence

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APA (6th Edition):

Chaabouni, S. (2017). Contribution à la chimie des cinnamates ortho-fonctionnalisés : Exploitation comme (1) précurseurs synthétiques d'hétérocycles, (2) antennes photoactivables de complexes d'ions lanthanides luminescents : Contribution to the chemistry of ortho-functionalized cinnamates : exploitation as (1) building blocks for heterocyclic synthesis, (2) photoactivatable sensitizers of luminescent lanthanide complexes. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2017TOU30104

Chicago Manual of Style (16th Edition):

Chaabouni, Slim. “Contribution à la chimie des cinnamates ortho-fonctionnalisés : Exploitation comme (1) précurseurs synthétiques d'hétérocycles, (2) antennes photoactivables de complexes d'ions lanthanides luminescents : Contribution to the chemistry of ortho-functionalized cinnamates : exploitation as (1) building blocks for heterocyclic synthesis, (2) photoactivatable sensitizers of luminescent lanthanide complexes.” 2017. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed December 08, 2019. http://www.theses.fr/2017TOU30104.

MLA Handbook (7th Edition):

Chaabouni, Slim. “Contribution à la chimie des cinnamates ortho-fonctionnalisés : Exploitation comme (1) précurseurs synthétiques d'hétérocycles, (2) antennes photoactivables de complexes d'ions lanthanides luminescents : Contribution to the chemistry of ortho-functionalized cinnamates : exploitation as (1) building blocks for heterocyclic synthesis, (2) photoactivatable sensitizers of luminescent lanthanide complexes.” 2017. Web. 08 Dec 2019.

Vancouver:

Chaabouni S. Contribution à la chimie des cinnamates ortho-fonctionnalisés : Exploitation comme (1) précurseurs synthétiques d'hétérocycles, (2) antennes photoactivables de complexes d'ions lanthanides luminescents : Contribution to the chemistry of ortho-functionalized cinnamates : exploitation as (1) building blocks for heterocyclic synthesis, (2) photoactivatable sensitizers of luminescent lanthanide complexes. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2017. [cited 2019 Dec 08]. Available from: http://www.theses.fr/2017TOU30104.

Council of Science Editors:

Chaabouni S. Contribution à la chimie des cinnamates ortho-fonctionnalisés : Exploitation comme (1) précurseurs synthétiques d'hétérocycles, (2) antennes photoactivables de complexes d'ions lanthanides luminescents : Contribution to the chemistry of ortho-functionalized cinnamates : exploitation as (1) building blocks for heterocyclic synthesis, (2) photoactivatable sensitizers of luminescent lanthanide complexes. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2017. Available from: http://www.theses.fr/2017TOU30104


University of New South Wales

7. Wood, Kasey Cherie. New heterocyclic systems derived from activated indoles.

Degree: Chemistry, 2010, University of New South Wales

 This thesis explores the use of activated 3-substituted-4,6-dimethoxyindoles in the preparation of new indole-based heterocyclic systems.Novel pyrrolo[a]indole dimers were synthesized via acid catalysed condensation of… (more)

Subjects/Keywords: 9H-Pyrrolo[1,2-a]indole; Activated indoles; Pyrrolo[a]indole; 1,7-annulated indoles

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APA (6th Edition):

Wood, K. C. (2010). New heterocyclic systems derived from activated indoles. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50214 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9092/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Wood, Kasey Cherie. “New heterocyclic systems derived from activated indoles.” 2010. Doctoral Dissertation, University of New South Wales. Accessed December 08, 2019. http://handle.unsw.edu.au/1959.4/50214 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9092/SOURCE02?view=true.

MLA Handbook (7th Edition):

Wood, Kasey Cherie. “New heterocyclic systems derived from activated indoles.” 2010. Web. 08 Dec 2019.

Vancouver:

Wood KC. New heterocyclic systems derived from activated indoles. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Dec 08]. Available from: http://handle.unsw.edu.au/1959.4/50214 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9092/SOURCE02?view=true.

Council of Science Editors:

Wood KC. New heterocyclic systems derived from activated indoles. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/50214 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9092/SOURCE02?view=true


Indian Institute of Science

8. Lanke, Veeranjaneyulu. Regioselective Functionalization of Indoles using Directing Group Strategy : An Efficient Transition Metal Catalysis.

Degree: 2016, Indian Institute of Science

 The thesis entitled “Regioselective Functionalization of Indoles using Directing Group Strategy: An Efficient Transition Metal Catalysis” is divided into two sections. Section A, which is… (more)

Subjects/Keywords: Regioselective Functionalization; Indoles; Transition Metal Catalysis; Regioselective Alkenylation; Alkenylation of Indoles; Directing Group Strategy; 4-Amino Indoles; Indoles at C2-position; Indoles at C4-position; C2 vs C4-alkenylation of Indoles; Organic Chemistry

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APA (6th Edition):

Lanke, V. (2016). Regioselective Functionalization of Indoles using Directing Group Strategy : An Efficient Transition Metal Catalysis. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/3070

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):

Lanke, Veeranjaneyulu. “Regioselective Functionalization of Indoles using Directing Group Strategy : An Efficient Transition Metal Catalysis.” 2016. Thesis, Indian Institute of Science. Accessed December 08, 2019. http://hdl.handle.net/2005/3070.

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

MLA Handbook (7th Edition):

Lanke, Veeranjaneyulu. “Regioselective Functionalization of Indoles using Directing Group Strategy : An Efficient Transition Metal Catalysis.” 2016. Web. 08 Dec 2019.

Vancouver:

Lanke V. Regioselective Functionalization of Indoles using Directing Group Strategy : An Efficient Transition Metal Catalysis. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2005/3070.

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

Council of Science Editors:

Lanke V. Regioselective Functionalization of Indoles using Directing Group Strategy : An Efficient Transition Metal Catalysis. [Thesis]. Indian Institute of Science; 2016. Available from: http://hdl.handle.net/2005/3070

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

9. Denizot, Natacha. Couplages oxydants entre indoles et phénols pour la synthèse de benzofuroindolines naturelles : Oxidative Coupling between Indoles and Phenols towards the Synthesis of Natural Benzofuroindolines.

Degree: Docteur es, Chimie, 2015, Paris Saclay

Le noyau benzofuro[2,3-b]indoline est une structure complexe que l’on retrouve dans différentes substances naturelles telles que l’azonazine, la voacalgine A, la bipleiophylline ou encore le… (more)

Subjects/Keywords: Benzofuroindolines; Couplage oxydant; Voacalgine A; Diazonamide A; Indoles; Phénols; Bromopyrroloindolines; Benzofuroindolines; Oxidative coupling; Voacalgine A; Diazonamide A; Indoles; Phenols; Bromopyrroloindolines

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APA (6th Edition):

Denizot, N. (2015). Couplages oxydants entre indoles et phénols pour la synthèse de benzofuroindolines naturelles : Oxidative Coupling between Indoles and Phenols towards the Synthesis of Natural Benzofuroindolines. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2015SACLS147

Chicago Manual of Style (16th Edition):

Denizot, Natacha. “Couplages oxydants entre indoles et phénols pour la synthèse de benzofuroindolines naturelles : Oxidative Coupling between Indoles and Phenols towards the Synthesis of Natural Benzofuroindolines.” 2015. Doctoral Dissertation, Paris Saclay. Accessed December 08, 2019. http://www.theses.fr/2015SACLS147.

MLA Handbook (7th Edition):

Denizot, Natacha. “Couplages oxydants entre indoles et phénols pour la synthèse de benzofuroindolines naturelles : Oxidative Coupling between Indoles and Phenols towards the Synthesis of Natural Benzofuroindolines.” 2015. Web. 08 Dec 2019.

Vancouver:

Denizot N. Couplages oxydants entre indoles et phénols pour la synthèse de benzofuroindolines naturelles : Oxidative Coupling between Indoles and Phenols towards the Synthesis of Natural Benzofuroindolines. [Internet] [Doctoral dissertation]. Paris Saclay; 2015. [cited 2019 Dec 08]. Available from: http://www.theses.fr/2015SACLS147.

Council of Science Editors:

Denizot N. Couplages oxydants entre indoles et phénols pour la synthèse de benzofuroindolines naturelles : Oxidative Coupling between Indoles and Phenols towards the Synthesis of Natural Benzofuroindolines. [Doctoral Dissertation]. Paris Saclay; 2015. Available from: http://www.theses.fr/2015SACLS147

10. Adouama, Cherif. Développement de méthodologies de SRN1 et de catalyse photoredox pour la synthèse d’indoles tétracycliques : Development of SRN1 and photoredox catalysis methodologies towards the synthesis of tetracyclic indoles.

Degree: Docteur es, Chimie. Chimie organique, 2018, Lyon

Le développement de nouvelles méthodologies de synthèse douces et soucieuses de l'environnement apparait de nos jours comme un véritable besoin. Dans ce contexte, la chimie… (more)

Subjects/Keywords: Indoles tétracycliques; Fluor; Chimie radicalaire; SRN1; Électrochimie; Catalyse photoredox; Photochimie; Tetracyclic indoles; Fluorine; Radical chemistry; SRN1; Electrochemistry; Photoredox catalysis; Photochemistry; 540

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APA (6th Edition):

Adouama, C. (2018). Développement de méthodologies de SRN1 et de catalyse photoredox pour la synthèse d’indoles tétracycliques : Development of SRN1 and photoredox catalysis methodologies towards the synthesis of tetracyclic indoles. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2018LYSE1223

Chicago Manual of Style (16th Edition):

Adouama, Cherif. “Développement de méthodologies de SRN1 et de catalyse photoredox pour la synthèse d’indoles tétracycliques : Development of SRN1 and photoredox catalysis methodologies towards the synthesis of tetracyclic indoles.” 2018. Doctoral Dissertation, Lyon. Accessed December 08, 2019. http://www.theses.fr/2018LYSE1223.

MLA Handbook (7th Edition):

Adouama, Cherif. “Développement de méthodologies de SRN1 et de catalyse photoredox pour la synthèse d’indoles tétracycliques : Development of SRN1 and photoredox catalysis methodologies towards the synthesis of tetracyclic indoles.” 2018. Web. 08 Dec 2019.

Vancouver:

Adouama C. Développement de méthodologies de SRN1 et de catalyse photoredox pour la synthèse d’indoles tétracycliques : Development of SRN1 and photoredox catalysis methodologies towards the synthesis of tetracyclic indoles. [Internet] [Doctoral dissertation]. Lyon; 2018. [cited 2019 Dec 08]. Available from: http://www.theses.fr/2018LYSE1223.

Council of Science Editors:

Adouama C. Développement de méthodologies de SRN1 et de catalyse photoredox pour la synthèse d’indoles tétracycliques : Development of SRN1 and photoredox catalysis methodologies towards the synthesis of tetracyclic indoles. [Doctoral Dissertation]. Lyon; 2018. Available from: http://www.theses.fr/2018LYSE1223


University of California – Berkeley

11. Wilkerson-Hill, SIdney Malik. Development and Applications of (Hetero)cycloisomerization Methodologies to Access Natural Product Scaffolds.

Degree: Chemistry, 2015, University of California – Berkeley

 The development of new heterocycloisomerization reactions as a tactic to access natural product scaffolds is an active area of research. Chapter 1 describes the development… (more)

Subjects/Keywords: Chemistry; benzofurans; cycloisomerization; indenes; indoles; natural products; tetrahydrofluorene

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APA (6th Edition):

Wilkerson-Hill, S. M. (2015). Development and Applications of (Hetero)cycloisomerization Methodologies to Access Natural Product Scaffolds. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/0sq7h2qd

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):

Wilkerson-Hill, SIdney Malik. “Development and Applications of (Hetero)cycloisomerization Methodologies to Access Natural Product Scaffolds.” 2015. Thesis, University of California – Berkeley. Accessed December 08, 2019. http://www.escholarship.org/uc/item/0sq7h2qd.

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

MLA Handbook (7th Edition):

Wilkerson-Hill, SIdney Malik. “Development and Applications of (Hetero)cycloisomerization Methodologies to Access Natural Product Scaffolds.” 2015. Web. 08 Dec 2019.

Vancouver:

Wilkerson-Hill SM. Development and Applications of (Hetero)cycloisomerization Methodologies to Access Natural Product Scaffolds. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2019 Dec 08]. Available from: http://www.escholarship.org/uc/item/0sq7h2qd.

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

Council of Science Editors:

Wilkerson-Hill SM. Development and Applications of (Hetero)cycloisomerization Methodologies to Access Natural Product Scaffolds. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/0sq7h2qd

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


University of Illinois – Chicago

12. Kuznetsov, Alexey. New Advances in the Synthesis of Siloles and N-Heterocycles.

Degree: 2014, University of Illinois – Chicago

 This thesis describes the development of novel transition-metal-catalyzed processes for the synthesis of dihydrobenzosiloles and fused heteroaromatic dihydrosiloles starting from aromatic- and heteroaromatic styrenes. It… (more)

Subjects/Keywords: Dihydrobenzosiloles; C-H Silylation; Furan Recyclization; Indoles; Diazocompounds; 1,2,3-Triazolines.

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APA (6th Edition):

Kuznetsov, A. (2014). New Advances in the Synthesis of Siloles and N-Heterocycles. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19016

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):

Kuznetsov, Alexey. “New Advances in the Synthesis of Siloles and N-Heterocycles.” 2014. Thesis, University of Illinois – Chicago. Accessed December 08, 2019. http://hdl.handle.net/10027/19016.

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

MLA Handbook (7th Edition):

Kuznetsov, Alexey. “New Advances in the Synthesis of Siloles and N-Heterocycles.” 2014. Web. 08 Dec 2019.

Vancouver:

Kuznetsov A. New Advances in the Synthesis of Siloles and N-Heterocycles. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10027/19016.

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

Council of Science Editors:

Kuznetsov A. New Advances in the Synthesis of Siloles and N-Heterocycles. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/19016

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


Université de Sherbrooke

13. Prévost, Julie. Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile .

Degree: 2012, Université de Sherbrooke

 Les travaux de recherche présentés dans cet ouvrage ont été effectués dans le but de développer des catalyseurs pour la réaction d'halolactonisation énantiosélective. Deux approches… (more)

Subjects/Keywords: Indoles; Diazirines; Acides phosphoriques; Acide de Bronsted; Benziodoxole; Fluororoiodane; Iodane; Halolactonisation

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APA (6th Edition):

Prévost, J. (2012). Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile . (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/5755

Chicago Manual of Style (16th Edition):

Prévost, Julie. “Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile .” 2012. Masters Thesis, Université de Sherbrooke. Accessed December 08, 2019. http://hdl.handle.net/11143/5755.

MLA Handbook (7th Edition):

Prévost, Julie. “Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile .” 2012. Web. 08 Dec 2019.

Vancouver:

Prévost J. Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile . [Internet] [Masters thesis]. Université de Sherbrooke; 2012. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/11143/5755.

Council of Science Editors:

Prévost J. Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile . [Masters Thesis]. Université de Sherbrooke; 2012. Available from: http://hdl.handle.net/11143/5755


NSYSU

14. Lo, Pei-Ching. Gold-Catalyzed Cyclization of N-(2-ethynylphenyl)-N-((methylthio)methyl)acetamide Derivatives with 1,3-Migration to Substituted indoles.

Degree: Master, Biological Sciences, 2018, NSYSU

 Molecules that contain the indole substructure exhibit a broad spectrum of biological activities, such as anti-cancer, anti-oxidant, anti-rheumatoidal, anti-HIV, anti-microbial, anti-inflamatory, analgesic, antipyretic, anti-convulsant and… (more)

Subjects/Keywords: acetamide; anti-cancer; substituted indoles; 1,3-migration; cyclization; gold catalyst

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APA (6th Edition):

Lo, P. (2018). Gold-Catalyzed Cyclization of N-(2-ethynylphenyl)-N-((methylthio)methyl)acetamide Derivatives with 1,3-Migration to Substituted indoles. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0230118-152148

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):

Lo, Pei-Ching. “Gold-Catalyzed Cyclization of N-(2-ethynylphenyl)-N-((methylthio)methyl)acetamide Derivatives with 1,3-Migration to Substituted indoles.” 2018. Thesis, NSYSU. Accessed December 08, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0230118-152148.

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

MLA Handbook (7th Edition):

Lo, Pei-Ching. “Gold-Catalyzed Cyclization of N-(2-ethynylphenyl)-N-((methylthio)methyl)acetamide Derivatives with 1,3-Migration to Substituted indoles.” 2018. Web. 08 Dec 2019.

Vancouver:

Lo P. Gold-Catalyzed Cyclization of N-(2-ethynylphenyl)-N-((methylthio)methyl)acetamide Derivatives with 1,3-Migration to Substituted indoles. [Internet] [Thesis]. NSYSU; 2018. [cited 2019 Dec 08]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0230118-152148.

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

Council of Science Editors:

Lo P. Gold-Catalyzed Cyclization of N-(2-ethynylphenyl)-N-((methylthio)methyl)acetamide Derivatives with 1,3-Migration to Substituted indoles. [Thesis]. NSYSU; 2018. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0230118-152148

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


Victoria University of Wellington

15. Woolner, Victoria. New Halogenated Secondary Metabolites from Red Algae of the South Pacific.

Degree: 2017, Victoria University of Wellington

 An NMR- and MS-directed study led to the isolation and structure elucidation of several halogenated secondary metabolites from a New Zealand and a Tongan red… (more)

Subjects/Keywords: Halogens; Terpenes; Indoles; Natural Products; Halogenated metabolites; Diterpenes

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APA (6th Edition):

Woolner, V. (2017). New Halogenated Secondary Metabolites from Red Algae of the South Pacific. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/6737

Chicago Manual of Style (16th Edition):

Woolner, Victoria. “New Halogenated Secondary Metabolites from Red Algae of the South Pacific.” 2017. Doctoral Dissertation, Victoria University of Wellington. Accessed December 08, 2019. http://hdl.handle.net/10063/6737.

MLA Handbook (7th Edition):

Woolner, Victoria. “New Halogenated Secondary Metabolites from Red Algae of the South Pacific.” 2017. Web. 08 Dec 2019.

Vancouver:

Woolner V. New Halogenated Secondary Metabolites from Red Algae of the South Pacific. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2017. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10063/6737.

Council of Science Editors:

Woolner V. New Halogenated Secondary Metabolites from Red Algae of the South Pacific. [Doctoral Dissertation]. Victoria University of Wellington; 2017. Available from: http://hdl.handle.net/10063/6737


University of British Columbia

16. Loh, John Wai-Choong. The auxin-like properties of potassium naphthenates and their effect on indole-3-acetic acid biosynthesis and degradation .

Degree: 1972, University of British Columbia

 The auxin-like properties of potassium naphthenates (KNap), and the effect of these compounds on indoleacetic acid (IAA) biosynthesis and degradation were examined. Chapter I. The… (more)

Subjects/Keywords: Potassium naphthenates.; Indole.; Indoles.

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APA (6th Edition):

Loh, J. W. (1972). The auxin-like properties of potassium naphthenates and their effect on indole-3-acetic acid biosynthesis and degradation . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/33401

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):

Loh, John Wai-Choong. “The auxin-like properties of potassium naphthenates and their effect on indole-3-acetic acid biosynthesis and degradation .” 1972. Thesis, University of British Columbia. Accessed December 08, 2019. http://hdl.handle.net/2429/33401.

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

MLA Handbook (7th Edition):

Loh, John Wai-Choong. “The auxin-like properties of potassium naphthenates and their effect on indole-3-acetic acid biosynthesis and degradation .” 1972. Web. 08 Dec 2019.

Vancouver:

Loh JW. The auxin-like properties of potassium naphthenates and their effect on indole-3-acetic acid biosynthesis and degradation . [Internet] [Thesis]. University of British Columbia; 1972. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2429/33401.

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

Council of Science Editors:

Loh JW. The auxin-like properties of potassium naphthenates and their effect on indole-3-acetic acid biosynthesis and degradation . [Thesis]. University of British Columbia; 1972. Available from: http://hdl.handle.net/2429/33401

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


University of Texas Southwestern Medical Center

17. Rogers, Jamie Lee 1985-. Chemistry to Biology and Back Again: Small Molecule Regulation of HIF Transcription Factors and the Development of a Platform for the Discovery of New Biocatalyzed Organic Transformations.

Degree: 2013, University of Texas Southwestern Medical Center

 This work is divided into two parts. The first is the description of the regulation of the hypoxic response pathway via small molecule inhibitors. The… (more)

Subjects/Keywords: Basic Helix-Loop-Helix Transcription Factors; Biocatalysis; Indoles

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APA (6th Edition):

Rogers, J. L. 1. (2013). Chemistry to Biology and Back Again: Small Molecule Regulation of HIF Transcription Factors and the Development of a Platform for the Discovery of New Biocatalyzed Organic Transformations. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2013-05-111

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):

Rogers, Jamie Lee 1985-. “Chemistry to Biology and Back Again: Small Molecule Regulation of HIF Transcription Factors and the Development of a Platform for the Discovery of New Biocatalyzed Organic Transformations.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed December 08, 2019. http://hdl.handle.net/2152.5/ETD-UTSWMED-2013-05-111.

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

MLA Handbook (7th Edition):

Rogers, Jamie Lee 1985-. “Chemistry to Biology and Back Again: Small Molecule Regulation of HIF Transcription Factors and the Development of a Platform for the Discovery of New Biocatalyzed Organic Transformations.” 2013. Web. 08 Dec 2019.

Vancouver:

Rogers JL1. Chemistry to Biology and Back Again: Small Molecule Regulation of HIF Transcription Factors and the Development of a Platform for the Discovery of New Biocatalyzed Organic Transformations. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2013-05-111.

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

Council of Science Editors:

Rogers JL1. Chemistry to Biology and Back Again: Small Molecule Regulation of HIF Transcription Factors and the Development of a Platform for the Discovery of New Biocatalyzed Organic Transformations. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2013-05-111

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


Boston University

18. Furst, Laura. Radical mediated heterocycle functionalization: methodology development and natural product synthesis.

Degree: PhD, Chemistry, 2013, Boston University

 Substituted heterocycles are common building-blocks for biologically relevant molecules and represent challenging synthetic targets. Due to limited methods available for their preparation and derivatization, direct… (more)

Subjects/Keywords: Chemistry; Bisindoles; Heterocycles; Indoles; Photoredox catalysis; Visible light

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APA (6th Edition):

Furst, L. (2013). Radical mediated heterocycle functionalization: methodology development and natural product synthesis. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/13121

Chicago Manual of Style (16th Edition):

Furst, Laura. “Radical mediated heterocycle functionalization: methodology development and natural product synthesis.” 2013. Doctoral Dissertation, Boston University. Accessed December 08, 2019. http://hdl.handle.net/2144/13121.

MLA Handbook (7th Edition):

Furst, Laura. “Radical mediated heterocycle functionalization: methodology development and natural product synthesis.” 2013. Web. 08 Dec 2019.

Vancouver:

Furst L. Radical mediated heterocycle functionalization: methodology development and natural product synthesis. [Internet] [Doctoral dissertation]. Boston University; 2013. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2144/13121.

Council of Science Editors:

Furst L. Radical mediated heterocycle functionalization: methodology development and natural product synthesis. [Doctoral Dissertation]. Boston University; 2013. Available from: http://hdl.handle.net/2144/13121


Université Paris-Sud – Paris XI

19. Cebrian-Torrejon, Gerardo. Phytochimie de Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chimie et pharmacochimie de la canthin-6-one : Phytochemistry of Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chemistry and pharmacochemistry of canthin-6-one.

Degree: Docteur es, Pharmacognosie, 2011, Université Paris-Sud – Paris XI

Les alcaloïdes canthin-6-one, 5-méthoxy-canthin-6-one et N-oxyde de canthin-6-one ainsi que l’alkylamide sanshool et trois coumarines ont été identifiés et quantifiés des écorces, feuilles (dans ce… (more)

Subjects/Keywords: Substances naturelles; Canthin-6-one; Βeta-carbolines; Indoles; Bischler-Napieraslki; Prénylation; Natural products; Alkaloids; Canthin-6-one; Βeta-carbolines; Indoles; Biomomethic chemistry; Bischler-Napierlaski; Rutaceae; Prenylation; Tuberculosis; Cancer; Chagas; Nematicide

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APA (6th Edition):

Cebrian-Torrejon, G. (2011). Phytochimie de Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chimie et pharmacochimie de la canthin-6-one : Phytochemistry of Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chemistry and pharmacochemistry of canthin-6-one. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA114844

Chicago Manual of Style (16th Edition):

Cebrian-Torrejon, Gerardo. “Phytochimie de Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chimie et pharmacochimie de la canthin-6-one : Phytochemistry of Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chemistry and pharmacochemistry of canthin-6-one.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed December 08, 2019. http://www.theses.fr/2011PA114844.

MLA Handbook (7th Edition):

Cebrian-Torrejon, Gerardo. “Phytochimie de Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chimie et pharmacochimie de la canthin-6-one : Phytochemistry of Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chemistry and pharmacochemistry of canthin-6-one.” 2011. Web. 08 Dec 2019.

Vancouver:

Cebrian-Torrejon G. Phytochimie de Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chimie et pharmacochimie de la canthin-6-one : Phytochemistry of Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chemistry and pharmacochemistry of canthin-6-one. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2019 Dec 08]. Available from: http://www.theses.fr/2011PA114844.

Council of Science Editors:

Cebrian-Torrejon G. Phytochimie de Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chimie et pharmacochimie de la canthin-6-one : Phytochemistry of Zanthoxylum chiloperone var. angustifolium (Rutaceae). Chemistry and pharmacochemistry of canthin-6-one. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA114844


Universidade Federal de Santa Maria

20. Adriane Sperança. Síntese de Seleno-Isoxazóis e Seleno-Indóis via Reações de Ciclização Intramolecular mediadas por Cloreto Férrico.

Degree: 2013, Universidade Federal de Santa Maria

This work reports the synthesis of a series of 4-organoselenyl-isoxazoles (19 examples), prepared via FeCl3/diorganyl diselenides-promoted intramolecular cyclization of alkynone O-metyloximas. In general, the selenyl-isoxazoles… (more)

Subjects/Keywords: cloreto férrico; ciclização; indóis; isoxazóis; QUIMICA; indoles; isoxazoles; cyclization; iron(III) chloride

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APA (6th Edition):

Sperança, A. (2013). Síntese de Seleno-Isoxazóis e Seleno-Indóis via Reações de Ciclização Intramolecular mediadas por Cloreto Férrico. (Thesis). Universidade Federal de Santa Maria. Retrieved from http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=5201

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):

Sperança, Adriane. “Síntese de Seleno-Isoxazóis e Seleno-Indóis via Reações de Ciclização Intramolecular mediadas por Cloreto Férrico.” 2013. Thesis, Universidade Federal de Santa Maria. Accessed December 08, 2019. http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=5201.

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

MLA Handbook (7th Edition):

Sperança, Adriane. “Síntese de Seleno-Isoxazóis e Seleno-Indóis via Reações de Ciclização Intramolecular mediadas por Cloreto Férrico.” 2013. Web. 08 Dec 2019.

Vancouver:

Sperança A. Síntese de Seleno-Isoxazóis e Seleno-Indóis via Reações de Ciclização Intramolecular mediadas por Cloreto Férrico. [Internet] [Thesis]. Universidade Federal de Santa Maria; 2013. [cited 2019 Dec 08]. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=5201.

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

Council of Science Editors:

Sperança A. Síntese de Seleno-Isoxazóis e Seleno-Indóis via Reações de Ciclização Intramolecular mediadas por Cloreto Férrico. [Thesis]. Universidade Federal de Santa Maria; 2013. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=5201

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

21. Nirmal T. Havannavar. Synthesis and pharmacological screening of substituted fluoro indoles;.

Degree: Pharmaceutical Sciences, 2015, Jawaharlal Nehru Technological University, Anantapuram

No newline

Summary and Conclusion - 164-167, references - 168-192

Advisors/Committee Members: Dr. L.V.G. Nargund and Dr. M. Lakshmi Narasu.

Subjects/Keywords: Fluoro Indoles; Pharmaceutical Sciences; Pharmacological Screening

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APA (6th Edition):

Havannavar, N. T. (2015). Synthesis and pharmacological screening of substituted fluoro indoles;. (Thesis). Jawaharlal Nehru Technological University, Anantapuram. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/42673

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):

Havannavar, Nirmal T.. “Synthesis and pharmacological screening of substituted fluoro indoles;.” 2015. Thesis, Jawaharlal Nehru Technological University, Anantapuram. Accessed December 08, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/42673.

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

MLA Handbook (7th Edition):

Havannavar, Nirmal T.. “Synthesis and pharmacological screening of substituted fluoro indoles;.” 2015. Web. 08 Dec 2019.

Vancouver:

Havannavar NT. Synthesis and pharmacological screening of substituted fluoro indoles;. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Anantapuram; 2015. [cited 2019 Dec 08]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/42673.

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

Council of Science Editors:

Havannavar NT. Synthesis and pharmacological screening of substituted fluoro indoles;. [Thesis]. Jawaharlal Nehru Technological University, Anantapuram; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/42673

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


University of Toledo

22. Rondo, Ryan Thomas. Development of Constrained Geometry Complexes of Group 4 and 5 Metals.

Degree: PhD, Chemistry, 2010, University of Toledo

  Constrained geometry catalysts (CGC) are known to be active in the polymerization and copolymerization of alkenes with a distinct control over polymer tacticity. The… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; constrained geometry complexes; constrained geometry catalysts; indoles; pyrroles; 3-methylindole; polymerization catalysts

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APA (6th Edition):

Rondo, R. T. (2010). Development of Constrained Geometry Complexes of Group 4 and 5 Metals. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1271686430

Chicago Manual of Style (16th Edition):

Rondo, Ryan Thomas. “Development of Constrained Geometry Complexes of Group 4 and 5 Metals.” 2010. Doctoral Dissertation, University of Toledo. Accessed December 08, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1271686430.

MLA Handbook (7th Edition):

Rondo, Ryan Thomas. “Development of Constrained Geometry Complexes of Group 4 and 5 Metals.” 2010. Web. 08 Dec 2019.

Vancouver:

Rondo RT. Development of Constrained Geometry Complexes of Group 4 and 5 Metals. [Internet] [Doctoral dissertation]. University of Toledo; 2010. [cited 2019 Dec 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1271686430.

Council of Science Editors:

Rondo RT. Development of Constrained Geometry Complexes of Group 4 and 5 Metals. [Doctoral Dissertation]. University of Toledo; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1271686430


University of Bradford

23. Saidykhan, A. Synthetic, spectroscopic and computational studies of aromatic compounds : structure, fragmentation and novel dimerisation of indoles under electrospray conditions, and innovative nitrogen to carbon rearrangement of orthogonally protected sulphonamides and related compounds.

Degree: PhD, 2015, University of Bradford

 The complementary value of vibrational spectroscopy and mass spectrometry in obtaining structural information on a range of tricyclic indoles with various ring patterns has been… (more)

Subjects/Keywords: Indoles; Tetrahydrocarbazoles; Mass Spectrometry; Aromatic Compounds; Vibrational Spectroscopy; Dimerisation; Electrospray; Fragmentation; Rearrangement; Sulphonamides.

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APA (6th Edition):

Saidykhan, A. (2015). Synthetic, spectroscopic and computational studies of aromatic compounds : structure, fragmentation and novel dimerisation of indoles under electrospray conditions, and innovative nitrogen to carbon rearrangement of orthogonally protected sulphonamides and related compounds. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/14428

Chicago Manual of Style (16th Edition):

Saidykhan, A. “Synthetic, spectroscopic and computational studies of aromatic compounds : structure, fragmentation and novel dimerisation of indoles under electrospray conditions, and innovative nitrogen to carbon rearrangement of orthogonally protected sulphonamides and related compounds.” 2015. Doctoral Dissertation, University of Bradford. Accessed December 08, 2019. http://hdl.handle.net/10454/14428.

MLA Handbook (7th Edition):

Saidykhan, A. “Synthetic, spectroscopic and computational studies of aromatic compounds : structure, fragmentation and novel dimerisation of indoles under electrospray conditions, and innovative nitrogen to carbon rearrangement of orthogonally protected sulphonamides and related compounds.” 2015. Web. 08 Dec 2019.

Vancouver:

Saidykhan A. Synthetic, spectroscopic and computational studies of aromatic compounds : structure, fragmentation and novel dimerisation of indoles under electrospray conditions, and innovative nitrogen to carbon rearrangement of orthogonally protected sulphonamides and related compounds. [Internet] [Doctoral dissertation]. University of Bradford; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10454/14428.

Council of Science Editors:

Saidykhan A. Synthetic, spectroscopic and computational studies of aromatic compounds : structure, fragmentation and novel dimerisation of indoles under electrospray conditions, and innovative nitrogen to carbon rearrangement of orthogonally protected sulphonamides and related compounds. [Doctoral Dissertation]. University of Bradford; 2015. Available from: http://hdl.handle.net/10454/14428

24. Revelou, Panagiota-Kyriaki. Απομόνωση βιοδραστικών ενώσεων από σταυρανθή λαχανικά: ταυτοποίηση και ποσοτικός προσδιορισμός με συνθετικές και φασματοσκοπικές τεχνικές.

Degree: 2018, Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών

 Vegetables of the Cruciferae family (order Brassicales) contain a number of organic compounds with biological activity. Among these are glucosinolates, which are found only in… (more)

Subjects/Keywords: Γλυκοζινολίτες; Ισοθειοκυανικές Ενώσεις; Ινδολικές Ενώσεις; Σταυρανθή Λαχανικά; Glucosinolates; Isothiocyanates; Indoles; Cruciferous vegetables

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APA (6th Edition):

Revelou, P. (2018). Απομόνωση βιοδραστικών ενώσεων από σταυρανθή λαχανικά: ταυτοποίηση και ποσοτικός προσδιορισμός με συνθετικές και φασματοσκοπικές τεχνικές. (Thesis). Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών. Retrieved from http://hdl.handle.net/10442/hedi/44569

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):

Revelou, Panagiota-Kyriaki. “Απομόνωση βιοδραστικών ενώσεων από σταυρανθή λαχανικά: ταυτοποίηση και ποσοτικός προσδιορισμός με συνθετικές και φασματοσκοπικές τεχνικές.” 2018. Thesis, Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών. Accessed December 08, 2019. http://hdl.handle.net/10442/hedi/44569.

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

MLA Handbook (7th Edition):

Revelou, Panagiota-Kyriaki. “Απομόνωση βιοδραστικών ενώσεων από σταυρανθή λαχανικά: ταυτοποίηση και ποσοτικός προσδιορισμός με συνθετικές και φασματοσκοπικές τεχνικές.” 2018. Web. 08 Dec 2019.

Vancouver:

Revelou P. Απομόνωση βιοδραστικών ενώσεων από σταυρανθή λαχανικά: ταυτοποίηση και ποσοτικός προσδιορισμός με συνθετικές και φασματοσκοπικές τεχνικές. [Internet] [Thesis]. Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών; 2018. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10442/hedi/44569.

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

Council of Science Editors:

Revelou P. Απομόνωση βιοδραστικών ενώσεων από σταυρανθή λαχανικά: ταυτοποίηση και ποσοτικός προσδιορισμός με συνθετικές και φασματοσκοπικές τεχνικές. [Thesis]. Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών; 2018. Available from: http://hdl.handle.net/10442/hedi/44569

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


Iowa State University

25. Caruthers, Heather Anne. Applications of Heterocyclic Synthesis.

Degree: 2009, Iowa State University

 Two applications of heterocyclic synthesis are discussed herein. Microwave-assisted synthesis leads to a variety of heterocyclic 2,3-disubstituted indoles in a fast and efficient manner. The… (more)

Subjects/Keywords: 2; 2'-dithiosuccinic anhydride; Biobased Linkers; Heterocyclic Indoles; Natural Product Synthesis; Staurosporine; Chemistry

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APA (6th Edition):

Caruthers, H. A. (2009). Applications of Heterocyclic Synthesis. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/10494

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):

Caruthers, Heather Anne. “Applications of Heterocyclic Synthesis.” 2009. Thesis, Iowa State University. Accessed December 08, 2019. https://lib.dr.iastate.edu/etd/10494.

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

MLA Handbook (7th Edition):

Caruthers, Heather Anne. “Applications of Heterocyclic Synthesis.” 2009. Web. 08 Dec 2019.

Vancouver:

Caruthers HA. Applications of Heterocyclic Synthesis. [Internet] [Thesis]. Iowa State University; 2009. [cited 2019 Dec 08]. Available from: https://lib.dr.iastate.edu/etd/10494.

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

Council of Science Editors:

Caruthers HA. Applications of Heterocyclic Synthesis. [Thesis]. Iowa State University; 2009. Available from: https://lib.dr.iastate.edu/etd/10494

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


University of Houston

26. Lundy, Brian J. I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY.

Degree: Chemistry, Department of, 2013, University of Houston

 This dissertation presents two different projects, the first being the use of boronic acids in conjugate addition reactions on different substituted indoles, and the second… (more)

Subjects/Keywords: organic chemistry; reaction development; conjugate addition; BINOL; boronic acids; indoles; total synthesis; natural products; Chemistry

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

APA (6th Edition):

Lundy, B. J. (2013). I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/950

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):

Lundy, Brian J. “I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY.” 2013. Thesis, University of Houston. Accessed December 08, 2019. http://hdl.handle.net/10657/950.

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

MLA Handbook (7th Edition):

Lundy, Brian J. “I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY.” 2013. Web. 08 Dec 2019.

Vancouver:

Lundy BJ. I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY. [Internet] [Thesis]. University of Houston; 2013. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10657/950.

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

Council of Science Editors:

Lundy BJ. I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY. [Thesis]. University of Houston; 2013. Available from: http://hdl.handle.net/10657/950

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


Duquesne University

27. Zaware, Nilesh. Synthesis of Pyrrolo[2,3-d]Pytimidines and Pytimido[4,5-b]Indoles as Inhibitors of Multiple Receptor Tyrosine Kinases, Folate Metabolizing Enzymes and Tubulin.

Degree: PhD, Medicinal Chemistry, 2009, Duquesne University

 This dissertation deals with the synthesis of substituted pyrrolo[2,3-d]pyrimidines and pyrimido[4,5-b]indoles as potential antitumor agents. The approaches to target tumor cells include inhibition of tumor… (more)

Subjects/Keywords: Antifolate; Antitubulin; pyrimido[4; 5-b]indoles; pyrrolo[2; 3-d]pyrimidines; Receptor tyrosine kinase

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

APA (6th Edition):

Zaware, N. (2009). Synthesis of Pyrrolo[2,3-d]Pytimidines and Pytimido[4,5-b]Indoles as Inhibitors of Multiple Receptor Tyrosine Kinases, Folate Metabolizing Enzymes and Tubulin. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1539

Chicago Manual of Style (16th Edition):

Zaware, Nilesh. “Synthesis of Pyrrolo[2,3-d]Pytimidines and Pytimido[4,5-b]Indoles as Inhibitors of Multiple Receptor Tyrosine Kinases, Folate Metabolizing Enzymes and Tubulin.” 2009. Doctoral Dissertation, Duquesne University. Accessed December 08, 2019. https://dsc.duq.edu/etd/1539.

MLA Handbook (7th Edition):

Zaware, Nilesh. “Synthesis of Pyrrolo[2,3-d]Pytimidines and Pytimido[4,5-b]Indoles as Inhibitors of Multiple Receptor Tyrosine Kinases, Folate Metabolizing Enzymes and Tubulin.” 2009. Web. 08 Dec 2019.

Vancouver:

Zaware N. Synthesis of Pyrrolo[2,3-d]Pytimidines and Pytimido[4,5-b]Indoles as Inhibitors of Multiple Receptor Tyrosine Kinases, Folate Metabolizing Enzymes and Tubulin. [Internet] [Doctoral dissertation]. Duquesne University; 2009. [cited 2019 Dec 08]. Available from: https://dsc.duq.edu/etd/1539.

Council of Science Editors:

Zaware N. Synthesis of Pyrrolo[2,3-d]Pytimidines and Pytimido[4,5-b]Indoles as Inhibitors of Multiple Receptor Tyrosine Kinases, Folate Metabolizing Enzymes and Tubulin. [Doctoral Dissertation]. Duquesne University; 2009. Available from: https://dsc.duq.edu/etd/1539


University of Florida

28. Stupp, Gregory S. Metabolomics as a Tool for Understanding Stress Responses in Caenorhabditis Elegans.

Degree: PhD, Medical Sciences - Biochemistry and Molecular Biology (IDP), 2014, University of Florida

 The nematode Caenorhabditis elegans is a widely studied model organism that has led to many important contributions to science. In its natural habitat, C. elegans… (more)

Subjects/Keywords: Carbon; Indoles; Ions; Mass spectroscopy; Metabolites; Metabolomics; Molecules; Phenazines; Roundworms; Worms; elegans  – iroa  – metabolomics  – phenazines

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

APA (6th Edition):

Stupp, G. S. (2014). Metabolomics as a Tool for Understanding Stress Responses in Caenorhabditis Elegans. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0047006

Chicago Manual of Style (16th Edition):

Stupp, Gregory S. “Metabolomics as a Tool for Understanding Stress Responses in Caenorhabditis Elegans.” 2014. Doctoral Dissertation, University of Florida. Accessed December 08, 2019. http://ufdc.ufl.edu/UFE0047006.

MLA Handbook (7th Edition):

Stupp, Gregory S. “Metabolomics as a Tool for Understanding Stress Responses in Caenorhabditis Elegans.” 2014. Web. 08 Dec 2019.

Vancouver:

Stupp GS. Metabolomics as a Tool for Understanding Stress Responses in Caenorhabditis Elegans. [Internet] [Doctoral dissertation]. University of Florida; 2014. [cited 2019 Dec 08]. Available from: http://ufdc.ufl.edu/UFE0047006.

Council of Science Editors:

Stupp GS. Metabolomics as a Tool for Understanding Stress Responses in Caenorhabditis Elegans. [Doctoral Dissertation]. University of Florida; 2014. Available from: http://ufdc.ufl.edu/UFE0047006

29. Amorde, Shawn Marie. A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine.

Degree: PhD, Chemistry, 2006, University of Texas – Austin

 Several novel cascade processes have been designed and developed that involve sequential reactions of imines and iminium ions to form substituted quinolizidine ring systems in… (more)

Subjects/Keywords: Quinolizidine alkaloids; Meloscine; Indoles; Synthesis

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APA (6th Edition):

Amorde, S. M. (2006). A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/20987

Chicago Manual of Style (16th Edition):

Amorde, Shawn Marie. “A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine.” 2006. Doctoral Dissertation, University of Texas – Austin. Accessed December 08, 2019. http://hdl.handle.net/2152/20987.

MLA Handbook (7th Edition):

Amorde, Shawn Marie. “A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine.” 2006. Web. 08 Dec 2019.

Vancouver:

Amorde SM. A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2006. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2152/20987.

Council of Science Editors:

Amorde SM. A cascade approach toward indolizidine and quinolizidine alkaloids : highlighted by the total syntheses of (±)-epilupinine, (±)-tashiromine, and (-)-epimyrtine progress toward the total synthesis of (±)-meloscine. [Doctoral Dissertation]. University of Texas – Austin; 2006. Available from: http://hdl.handle.net/2152/20987

30. Kushwaha, Upendra Kumar. Synthesis of newer indoles phenothiazines napthalenes quinazolinones and anthranilic acid as anti inflammatory agents;.

Degree: Chemistry, 2014, Chaudhary Charan Singh University

None newline

Summary p.1-13, Bibliography p. 196-221

Advisors/Committee Members: Owardhana, Yesh.

Subjects/Keywords: Synthesis; Newer Indoles; Phenothiazines Napthalenes; Quinazolinones; Anthranilic Acid

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APA (6th Edition):

Kushwaha, U. K. (2014). Synthesis of newer indoles phenothiazines napthalenes quinazolinones and anthranilic acid as anti inflammatory agents;. (Thesis). Chaudhary Charan Singh University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/22657

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):

Kushwaha, Upendra Kumar. “Synthesis of newer indoles phenothiazines napthalenes quinazolinones and anthranilic acid as anti inflammatory agents;.” 2014. Thesis, Chaudhary Charan Singh University. Accessed December 08, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/22657.

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

MLA Handbook (7th Edition):

Kushwaha, Upendra Kumar. “Synthesis of newer indoles phenothiazines napthalenes quinazolinones and anthranilic acid as anti inflammatory agents;.” 2014. Web. 08 Dec 2019.

Vancouver:

Kushwaha UK. Synthesis of newer indoles phenothiazines napthalenes quinazolinones and anthranilic acid as anti inflammatory agents;. [Internet] [Thesis]. Chaudhary Charan Singh University; 2014. [cited 2019 Dec 08]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/22657.

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

Council of Science Editors:

Kushwaha UK. Synthesis of newer indoles phenothiazines napthalenes quinazolinones and anthranilic acid as anti inflammatory agents;. [Thesis]. Chaudhary Charan Singh University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/22657

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

[1] [2] [3]

.