subject:(Carbocycles)

University of Alberta

1. Sunasee, Rajesh. Methodology and natural product synthesis: carbocycles, culpin and sorbicillactone A.

Degree: PhD, Department of Chemistry, 2009, University of Alberta

URL: https://era.library.ualberta.ca/files/xp68kg66z

► The first chapter of this thesis describes the development of a general method for indirectly effecting radical carbocyclization of an alkyl chain onto an aromatic… (more)

Subjects/Keywords: sorbicillactone A; bismuth trichloride; culpin; desymmetrization; carbocycles

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APA (6^th Edition):

Sunasee, R. (2009). Methodology and natural product synthesis: carbocycles, culpin and sorbicillactone A. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/xp68kg66z

Chicago Manual of Style (16^th Edition):

Sunasee, Rajesh. “Methodology and natural product synthesis: carbocycles, culpin and sorbicillactone A.” 2009. Doctoral Dissertation, University of Alberta. Accessed January 20, 2021. https://era.library.ualberta.ca/files/xp68kg66z.

MLA Handbook (7^th Edition):

Sunasee, Rajesh. “Methodology and natural product synthesis: carbocycles, culpin and sorbicillactone A.” 2009. Web. 20 Jan 2021.

Vancouver:

Sunasee R. Methodology and natural product synthesis: carbocycles, culpin and sorbicillactone A. [Internet] [Doctoral dissertation]. University of Alberta; 2009. [cited 2021 Jan 20]. Available from: https://era.library.ualberta.ca/files/xp68kg66z.

Council of Science Editors:

Sunasee R. Methodology and natural product synthesis: carbocycles, culpin and sorbicillactone A. [Doctoral Dissertation]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/xp68kg66z

The Ohio State University

2. Miller, Donald Bruce. Structure and chemistry of photodimers of trans-beta-nitrostyrene.

Degree: PhD, Graduate School, 1957, The Ohio State University

URL: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486468562984502

Subjects/Keywords: Chemistry; Nitrostyrene; Carbocycles

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APA (6^th Edition):

Miller, D. B. (1957). Structure and chemistry of photodimers of trans-beta-nitrostyrene. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1486468562984502

Chicago Manual of Style (16^th Edition):

Miller, Donald Bruce. “Structure and chemistry of photodimers of trans-beta-nitrostyrene.” 1957. Doctoral Dissertation, The Ohio State University. Accessed January 20, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486468562984502.

MLA Handbook (7^th Edition):

Miller, Donald Bruce. “Structure and chemistry of photodimers of trans-beta-nitrostyrene.” 1957. Web. 20 Jan 2021.

Vancouver:

Miller DB. Structure and chemistry of photodimers of trans-beta-nitrostyrene. [Internet] [Doctoral dissertation]. The Ohio State University; 1957. [cited 2021 Jan 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486468562984502.

Council of Science Editors:

Miller DB. Structure and chemistry of photodimers of trans-beta-nitrostyrene. [Doctoral Dissertation]. The Ohio State University; 1957. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486468562984502

University of Alberta

3. Sreedharan, Dinesh. Asymmetric Synthesis of Carbocycles by Intramolecular Conjugate Displacement & Synthetic Studies on Sorbicillactone A.

Degree: PhD, Department of Chemistry, 2013, University of Alberta

URL: https://era.library.ualberta.ca/files/ccc08hf63g

► The first chapter of this thesis describes an intramolecular conjugate displacement (ICD) for the asymmetric synthesis of carbocycles using a carbon nucleophile. The precursors for… (more)

Subjects/Keywords: asymmetric synthesis of carbocycles; optically pure carbocycles; intramolecular conjugate displacement; sorbicillactone A

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APA (6^th Edition):

Sreedharan, D. (2013). Asymmetric Synthesis of Carbocycles by Intramolecular Conjugate Displacement & Synthetic Studies on Sorbicillactone A. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/ccc08hf63g

Chicago Manual of Style (16^th Edition):

Sreedharan, Dinesh. “Asymmetric Synthesis of Carbocycles by Intramolecular Conjugate Displacement & Synthetic Studies on Sorbicillactone A.” 2013. Doctoral Dissertation, University of Alberta. Accessed January 20, 2021. https://era.library.ualberta.ca/files/ccc08hf63g.

MLA Handbook (7^th Edition):

Sreedharan, Dinesh. “Asymmetric Synthesis of Carbocycles by Intramolecular Conjugate Displacement & Synthetic Studies on Sorbicillactone A.” 2013. Web. 20 Jan 2021.

Vancouver:

Sreedharan D. Asymmetric Synthesis of Carbocycles by Intramolecular Conjugate Displacement & Synthetic Studies on Sorbicillactone A. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2021 Jan 20]. Available from: https://era.library.ualberta.ca/files/ccc08hf63g.

Council of Science Editors:

Sreedharan D. Asymmetric Synthesis of Carbocycles by Intramolecular Conjugate Displacement & Synthetic Studies on Sorbicillactone A. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/ccc08hf63g

4. Liu, Rui. Ruthenium (II) - catalysed enyne carbocyclization reactions : Carbocyclisations d’énynes catalysées par les complexes du ruthénium.

Degree: Docteur es, Sciences Chimiques, 2017, Ecole centrale de Marseille

URL: http://www.theses.fr/2017ECDM0004

►

Cette thèse porte sur les réactions de cyclisation des 1,6-enynes impliquant des catalyseurs de ruthénium. Trois types différents de cyclisation ont été élaborés à partir… (more)

▼

Cette thèse porte sur les réactions de cyclisation des 1,6-enynes impliquant des catalyseurs de ruthénium. Trois types différents de cyclisation ont été élaborés à partir de précurseurs facilement disponibles, tels que les 1,6-enynes et alcynes. Dans un premier temps, une nouvelle cyclisation hydroalcynylante des 1,6-enynes, à l'aide d'alcynes terminaux comme co-réactifs, catalysée par le ruthenium a été explorée. Cette réaction fournit une méthode de synthèse de cycles à cinq chaînons doté d'un motif 1,5-enyne exocyclique. Un complexe du ruthenium neutre et riche en électrons, Cp*Ru(cod)Cl, s'est avéré être le catalyseur de choix de ces transformations. Dans un deuxième temps, en utilisant le même complexe, la cycloaddition [2+2+2] des 1,6-enynes et alcynes catalysée par le ruthénium a été développée. Les alcynes internes et terminaux sont appropriés pour accéder en une seule étape aux bicyclohexadienes avec de hauts rendements. Une bicycloannulation inhabitelle des 1,6-enynes, intégrant un atome d’azote, catalysée par le ruthénium a également été élaborée. Pour ces cyclisations, seul un complexe du ruthénium électrophile et alkynophile tel que [RuCl2(CO)3]2 a été en mesure d'effectuer la réaction. La formation exclusive des 3-azabicylo[4.1.0]hept-1-enes a été observée avec les 1,6-enynes dotés d'une unité alcyne interne. Ces réactions de cyclisation, respectant le principe des réactions à économie d’atome, sont discutées et sur la base de leur mécanisme de formation.

This dissertation focuses on cyclization reactions of 1,6-enynes involving ruthenium catalysts. Three different types of cyclization were developed from readily available precursors, such as 1,6-enynes and alkynes. In one application, a novel ruthenium-catalyzed hydroalkynylative cyclization of 1,6-enynes using terminal alkynes as co-reactants was explored. This reaction provides and entry to five-membered rings featuring an exocyclic 1,5-enyne motif. A neutral electron-rich ruthenium complex Cp*Ru(cod)Cl proved to be the catalyst of choice for these transformations. In another application, using the same complex, the ruthenium-catalyzed [2+2+2] cycloaddition of 1,6-enynes and alkynes was developed. Both internal and terminal alkynes were suitable substrates to access bicyclohexadienes with high yields in a single step. An intriguing ruthenium-catalyzed bicycloannulation of nitrogen-tethered 1,6-enynes has also been developed. For these cyclizations, only the electrophilic and alkynophilic ruthenium complex [RuCl2(CO)3]2 was able to perform the reaction. The exclusive formation of 3-azabicylo[4.1.0]hept-1-enes was observed with 1,6-enynes featuring an internal alkyne unit. These cyclization reactions fulfil the atom-economical reactions principle and are discussed on the basis of their mechanisms of formation.

Advisors/Committee Members: Tenaglia, Alphonse (thesis director), Giordano, Laurent (thesis director).

Subjects/Keywords: Énynes; Catalyse; Ruthénium; Cycles carbonés; Enynes; Catalysis; Ruthenium; Carbocycles

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APA (6^th Edition):

Liu, R. (2017). Ruthenium (II) - catalysed enyne carbocyclization reactions : Carbocyclisations d’énynes catalysées par les complexes du ruthénium. (Doctoral Dissertation). Ecole centrale de Marseille. Retrieved from http://www.theses.fr/2017ECDM0004

Chicago Manual of Style (16^th Edition):

Liu, Rui. “Ruthenium (II) - catalysed enyne carbocyclization reactions : Carbocyclisations d’énynes catalysées par les complexes du ruthénium.” 2017. Doctoral Dissertation, Ecole centrale de Marseille. Accessed January 20, 2021. http://www.theses.fr/2017ECDM0004.

MLA Handbook (7^th Edition):

Liu, Rui. “Ruthenium (II) - catalysed enyne carbocyclization reactions : Carbocyclisations d’énynes catalysées par les complexes du ruthénium.” 2017. Web. 20 Jan 2021.

Vancouver:

Liu R. Ruthenium (II) - catalysed enyne carbocyclization reactions : Carbocyclisations d’énynes catalysées par les complexes du ruthénium. [Internet] [Doctoral dissertation]. Ecole centrale de Marseille; 2017. [cited 2021 Jan 20]. Available from: http://www.theses.fr/2017ECDM0004.

Council of Science Editors:

Liu R. Ruthenium (II) - catalysed enyne carbocyclization reactions : Carbocyclisations d’énynes catalysées par les complexes du ruthénium. [Doctoral Dissertation]. Ecole centrale de Marseille; 2017. Available from: http://www.theses.fr/2017ECDM0004

5. Ramann, Ginelle A. Quinolines: Novel Synthesis and Derivatives of Heterocyclic Bioactive Agents.

Degree: PhD, Chemistry and Biochemistry, 2016, U of Denver

URL: https://digitalcommons.du.edu/etd/1116

► Tuberculosis is a pulmonary disease that has ravaged the world throughout history. Even today, many developed and developing countries are experiencing this plight, made… (more)

▼ Tuberculosis is a pulmonary disease that has ravaged the world throughout history. Even today, many developed and developing countries are experiencing this plight, made worse by the scourge of antibiotic-resistant bacteria. Mycobacterium tuberculosis's class II fructose-1,6-bisphosphate aldolase presents an interesting target in the design of new therapies against this disease. Previous attempts to construct an inhibitor to this enzyme fell short due to poor selectivity or poor cellular uptake. However a new class of noncompetitive inhibitor based on 8-hydoxyquinoline-2-carboxylic acid presents a fresh approach. Preliminary studies indicate various modifications to this scaffold could be beneficial to its inhibitory efficacy. Modifications made to the phenol ring of the quinoline included small hydrophobic moieties such as methyl groups and fluorine. Additionally various carboxylic acid derivatives were installed next to the nitrogen of the heteroring. These derivatives included esters, amides, carbamates and ureas, and heterocycles. Biochemical testing of these compounds is ongoing but is already showing promising results. Many methods exist for the construction of quinoline rings systems, which can be utilized based on the pattern of substitution desired. Synthesis of heteroring-unsubstituted quinolines, however, has historically presented more of a challenge. Herein is described a novel method of cyclizing anilines with acrolein diethyl acetal to form these desired structures. This method produces quinolines with various substitutions on the phenyl ring in moderate to high yields without the use of harsh oxidants, extended reaction times, or organic solvents. The Lewis base-catalyzed annulation of allenoates with alkene acceptors in [3+2] cycloadditions is a new but burgeoning field. Many acceptors have been used in these reactions, but the use of quinones is unprecedented. Due to the highly reactive nature of quinones, it became necessary to screen various Lewis bases that would catalyze the reaction without being oxidized by the quinone. This is an ongoing investigation but is promising in the production of novel carbocycles that have potential benefits in medicinal chemistry. Advisors/Committee Members: Bryan J. Cowen, Ph.D..

Subjects/Keywords: Novel carbocycles; Medicinal chemistry; Quinones; Chemistry; Organic Chemistry

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APA (6^th Edition):

Ramann, G. A. (2016). Quinolines: Novel Synthesis and Derivatives of Heterocyclic Bioactive Agents. (Doctoral Dissertation). U of Denver. Retrieved from https://digitalcommons.du.edu/etd/1116

Chicago Manual of Style (16^th Edition):

Ramann, Ginelle A. “Quinolines: Novel Synthesis and Derivatives of Heterocyclic Bioactive Agents.” 2016. Doctoral Dissertation, U of Denver. Accessed January 20, 2021. https://digitalcommons.du.edu/etd/1116.

MLA Handbook (7^th Edition):

Ramann, Ginelle A. “Quinolines: Novel Synthesis and Derivatives of Heterocyclic Bioactive Agents.” 2016. Web. 20 Jan 2021.

Vancouver:

Ramann GA. Quinolines: Novel Synthesis and Derivatives of Heterocyclic Bioactive Agents. [Internet] [Doctoral dissertation]. U of Denver; 2016. [cited 2021 Jan 20]. Available from: https://digitalcommons.du.edu/etd/1116.

Council of Science Editors:

Ramann GA. Quinolines: Novel Synthesis and Derivatives of Heterocyclic Bioactive Agents. [Doctoral Dissertation]. U of Denver; 2016. Available from: https://digitalcommons.du.edu/etd/1116

University of Western Ontario

6. Piotrowski, Mathew L. The Synthesis of Heterocycles and Carbocycles and Work Towards Kainic Acid.

Degree: 2019, University of Western Ontario

URL: https://ir.lib.uwo.ca/etd/6641

► This thesis focuses on the synthesis of a variety of heterocycles and carbocycles such as pyrrolidines, dihydrofurans, dihydropyrroles, cyclopentenes, and 2,5-dihydrooxepines. Traditional synthetic methods are… (more)

▼ This thesis focuses on the synthesis of a variety of heterocycles and carbocycles such as pyrrolidines, dihydrofurans, dihydropyrroles, cyclopentenes, and 2,5-dihydrooxepines. Traditional synthetic methods are discussed first, followed by the manipulation of donor-acceptor cyclopropanes towards the above-mentioned compounds. This leads to a discussion about an important pyrrolidine-containing natural product known as kainic acid. Kainic acid has been studied in the neuroscience field for its biological properties which have led to a better understanding of common human neurological disorders like epilepsy, Huntington’s disease and the after-effects of strokes. Chapter two focuses on a common rearrangement of donor-acceptor cyclopropanes known as the Cloke-Wilson reaction. Without isolating the desired cyclopropane, two modes of reactivity were observed which depended solely on the choice of starting reagent. The first was the traditional Cloke-Wilson rearrangement generating dihydrofurans and the second was a vinylogous variant forming 2,5-dihydrooxepines. It was discovered that with careful choice of Lewis acid or transition metal catalysts, each of the obtained compounds can be manipulated to other dihydrofuran derivatives or dihydropyrrole heterocycles. One of the dihydropyrrole compounds obtained was deemed as a viable synthetic precursor towards kainic acid. Chapter three describes the synthetic efforts towards kainic acid utilizing the methodology from chapter two. The difficulties towards this natural molecule will be presented with the major issue resulting from stereochemical constraints. This resulted in the successful synthesis of β-allokainic acid which is one of the less active isomers of naturally occurring kainic acid. Chapter four discloses a single-step manipulation of the dihydrofurans synthesized via Cloke-Wilson rearrangement to their corresponding cyclopentenes. Extensive screening of Lewis acids and solvents provided insights into the possible mechanism of this reaction.

Subjects/Keywords: Donor-Acceptor Cyclopropanes; Kainic Acid; Cloke-Wilson Rearrangement; Heterocycles; Carbocycles; Rearrangement Reactions; Organic Chemistry

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APA (6^th Edition):

Piotrowski, M. L. (2019). The Synthesis of Heterocycles and Carbocycles and Work Towards Kainic Acid. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/6641

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

Chicago Manual of Style (16^th Edition):

Piotrowski, Mathew L. “The Synthesis of Heterocycles and Carbocycles and Work Towards Kainic Acid.” 2019. Thesis, University of Western Ontario. Accessed January 20, 2021. https://ir.lib.uwo.ca/etd/6641.

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

MLA Handbook (7^th Edition):

Piotrowski, Mathew L. “The Synthesis of Heterocycles and Carbocycles and Work Towards Kainic Acid.” 2019. Web. 20 Jan 2021.

Vancouver:

Piotrowski ML. The Synthesis of Heterocycles and Carbocycles and Work Towards Kainic Acid. [Internet] [Thesis]. University of Western Ontario; 2019. [cited 2021 Jan 20]. Available from: https://ir.lib.uwo.ca/etd/6641.

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

Council of Science Editors:

Piotrowski ML. The Synthesis of Heterocycles and Carbocycles and Work Towards Kainic Acid. [Thesis]. University of Western Ontario; 2019. Available from: https://ir.lib.uwo.ca/etd/6641

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

7. Deb, Biswajit. Investigations on oxoketene S,S_agetals newer synthetic methods for novel carbocycles and heterocycles; -.

Degree: Chemistry, 1990, North-Eastern Hill University

URL: http://shodhganga.inflibnet.ac.in/handle/10603/54758

Abstract available newline newline

-

Advisors/Committee Members: Ila, H.

Subjects/Keywords: Investigations; Oxoketene S; S_agetals; Novel Carbocycles; Heterocycles

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APA (6^th Edition):

Deb, B. (1990). Investigations on oxoketene S,S_agetals newer synthetic methods for novel carbocycles and heterocycles; -. (Thesis). North-Eastern Hill University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/54758

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

Chicago Manual of Style (16^th Edition):

Deb, Biswajit. “Investigations on oxoketene S,S_agetals newer synthetic methods for novel carbocycles and heterocycles; -.” 1990. Thesis, North-Eastern Hill University. Accessed January 20, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/54758.

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

MLA Handbook (7^th Edition):

Deb, Biswajit. “Investigations on oxoketene S,S_agetals newer synthetic methods for novel carbocycles and heterocycles; -.” 1990. Web. 20 Jan 2021.

Vancouver:

Deb B. Investigations on oxoketene S,S_agetals newer synthetic methods for novel carbocycles and heterocycles; -. [Internet] [Thesis]. North-Eastern Hill University; 1990. [cited 2021 Jan 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54758.

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

Council of Science Editors:

Deb B. Investigations on oxoketene S,S_agetals newer synthetic methods for novel carbocycles and heterocycles; -. [Thesis]. North-Eastern Hill University; 1990. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54758

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

8. Kishore, Kaushal. New synthetic routes to carbocycles and heterocycles via alpha_oxoketene dithioacetals; -.

Degree: Chemistry, 1999, North-Eastern Hill University

URL: http://shodhganga.inflibnet.ac.in/handle/10603/54927

Abstract not available newline newline

-

Advisors/Committee Members: Ila, H, Junjappa, H.

Subjects/Keywords: New Synthetic Routes; Carbocycles; Heterocycles; Alpha_Oxoketene Dithioacetals

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APA (6^th Edition):

Kishore, K. (1999). New synthetic routes to carbocycles and heterocycles via alpha_oxoketene dithioacetals; -. (Thesis). North-Eastern Hill University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/54927

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

Chicago Manual of Style (16^th Edition):

Kishore, Kaushal. “New synthetic routes to carbocycles and heterocycles via alpha_oxoketene dithioacetals; -.” 1999. Thesis, North-Eastern Hill University. Accessed January 20, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/54927.

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

MLA Handbook (7^th Edition):

Kishore, Kaushal. “New synthetic routes to carbocycles and heterocycles via alpha_oxoketene dithioacetals; -.” 1999. Web. 20 Jan 2021.

Vancouver:

Kishore K. New synthetic routes to carbocycles and heterocycles via alpha_oxoketene dithioacetals; -. [Internet] [Thesis]. North-Eastern Hill University; 1999. [cited 2021 Jan 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54927.

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

Council of Science Editors:

Kishore K. New synthetic routes to carbocycles and heterocycles via alpha_oxoketene dithioacetals; -. [Thesis]. North-Eastern Hill University; 1999. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54927

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

9. Sriram, V. Synthetic studies on alpha_oxoketene, dithioacetals; -.

Degree: Chemistry, 1999, North-Eastern Hill University

URL: http://shodhganga.inflibnet.ac.in/handle/10603/55252

Abstract available newline newline

-

Advisors/Committee Members: Ila, H.

Subjects/Keywords: Synthetic Studies; Alpha-Oxoketene; Dithioacetals; Carbocycles; Heterocycles; Nucleophiles

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APA (6^th Edition):

Sriram, V. (1999). Synthetic studies on alpha_oxoketene, dithioacetals; -. (Thesis). North-Eastern Hill University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/55252

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

Chicago Manual of Style (16^th Edition):

Sriram, V. “Synthetic studies on alpha_oxoketene, dithioacetals; -.” 1999. Thesis, North-Eastern Hill University. Accessed January 20, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/55252.

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

MLA Handbook (7^th Edition):

Sriram, V. “Synthetic studies on alpha_oxoketene, dithioacetals; -.” 1999. Web. 20 Jan 2021.

Vancouver:

Sriram V. Synthetic studies on alpha_oxoketene, dithioacetals; -. [Internet] [Thesis]. North-Eastern Hill University; 1999. [cited 2021 Jan 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/55252.

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

Council of Science Editors:

Sriram V. Synthetic studies on alpha_oxoketene, dithioacetals; -. [Thesis]. North-Eastern Hill University; 1999. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/55252

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

Iowa State University

10. Mehta, Saurabh. Palladium-catalyzed and electrophilic cyclization approaches to important heterocycles and carbocycles.

Degree: 2009, Iowa State University

URL: https://lib.dr.iastate.edu/etd/10951

► Several new and synthetically useful approaches involving palladium catalysis and electrophilic cyclization have been described for the synthesis of potentially medicinally and industrially important heterocycles… (more)

Subjects/Keywords: Carbocycles; Cyclization; Electrophilic; Heterocycles; Iodine; Palladium; Chemistry

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APA (6^th Edition):

Mehta, S. (2009). Palladium-catalyzed and electrophilic cyclization approaches to important heterocycles and carbocycles. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/10951

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

Chicago Manual of Style (16^th Edition):

Mehta, Saurabh. “Palladium-catalyzed and electrophilic cyclization approaches to important heterocycles and carbocycles.” 2009. Thesis, Iowa State University. Accessed January 20, 2021. https://lib.dr.iastate.edu/etd/10951.

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

MLA Handbook (7^th Edition):

Mehta, Saurabh. “Palladium-catalyzed and electrophilic cyclization approaches to important heterocycles and carbocycles.” 2009. Web. 20 Jan 2021.

Vancouver:

Mehta S. Palladium-catalyzed and electrophilic cyclization approaches to important heterocycles and carbocycles. [Internet] [Thesis]. Iowa State University; 2009. [cited 2021 Jan 20]. Available from: https://lib.dr.iastate.edu/etd/10951.

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

Council of Science Editors:

Mehta S. Palladium-catalyzed and electrophilic cyclization approaches to important heterocycles and carbocycles. [Thesis]. Iowa State University; 2009. Available from: https://lib.dr.iastate.edu/etd/10951

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

University of Kansas

11. Sherrill, William M. Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles.

Degree: PhD, Chemistry, 2009, University of Kansas

URL: http://hdl.handle.net/1808/5260

► This document deals with 3-membered carbocycles; their use as ligands for the asymmetric Heck reaction (AHR), the development of novel methods for their synthesis, and… (more)

Subjects/Keywords: Organic chemistry; Asymmetric; Carbocycles; Cyclopropene; Heck reaction; Hydroformylation; Synthesis

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APA (6^th Edition):

Sherrill, W. M. (2009). Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/5260

Chicago Manual of Style (16^th Edition):

Sherrill, William M. “Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles.” 2009. Doctoral Dissertation, University of Kansas. Accessed January 20, 2021. http://hdl.handle.net/1808/5260.

MLA Handbook (7^th Edition):

Sherrill, William M. “Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles.” 2009. Web. 20 Jan 2021.

Vancouver:

Sherrill WM. Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles. [Internet] [Doctoral dissertation]. University of Kansas; 2009. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1808/5260.

Council of Science Editors:

Sherrill WM. Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles. [Doctoral Dissertation]. University of Kansas; 2009. Available from: http://hdl.handle.net/1808/5260

12. Αφρουδάκης, Παντελεήμων. Σχεδιασμός και σύνθεση νέων ετεροκυκλικών και καρβοκυκλικών ενώσεων με μελατονινεργική δράση.

Degree: 2011, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

URL: http://hdl.handle.net/10442/hedi/35232

► In the context of this PhD thesis, the synthesis of a series of fused aromatic carbocyclic and heterocyclic melatoninergic compounds has been undertaken.In the introductory… (more)

▼ In the context of this PhD thesis, the synthesis of a series of fused aromatic carbocyclic and heterocyclic melatoninergic compounds has been undertaken.In the introductory chapter, an account of the endocrinological role of the hormone melatonin in mammals, followed by its therapeutic uses in man, is given. Next, a description of the receptors of melatonin is presented and some of the most interesting published melatoninergics are quoted. The introduction is concluded by a brief albeit detailed description of the aims of the present thesis and the design of the new compounds.In the subsequent chapter, a thorough description of the synthetic routes followed for the preparation of the new molecules, is given. The new melatoninergics belong to various chemical classes, which involve the conformationally constrained indole analogues 5 and 6, the tetracyclic compounds II, 12, 13 and 17, their analogues 25-27, 31, 32, 46-48, 53-55 and 39-41 and 65. Apart from these series, new cyclobuta- and cycloheptarenes, compounds 69-71, 77-79, 81-83, 87-89 and 102-104, 114-116, respectively were also prepared. The synthetic part of this chapter is concluded with the methods of preparation of the benzocycloheptenes 96-98 and 111-113.The new molecules were tested for their pharmacological activity, using the well-established Xenopus laevis pigment aggregation model. The indole analogues 5 and 6 are melatonin receptor agonists, with an affinity higher than that of melatonin. The tetracyclic compounds 12 and 13 are melatonin receptor agonists, whilst their gem-dimethyl side chain substituted congeners, II and 17, are partial agonists. Their analogues 25-27, 31, 32, 46-48, exhibit variable melatonin receptor activity ranging from pure agonistic (25-27) to pure antagonistic 31, 32, 46-48 and 53-55. Conversely, their congeners 39-41 and 65 are all pure antagonists. The action of the cyclobutarenes 69-71, 77-79, 81-83, 87-89 varies in accordance with the number of MeO substituents on the benzene nucleus and/or the length of the R group in the side chain. Thus, all the R2 (77-79) and R3 (81-83) monomethoxylated analogues are agonists. Conversely, with the exception of compound 69, their R1 monomethoxylated congeners 70 and 71 are partial agonists. The bis-methoxylated cyclobutarenes 88 and 89 are melatonin receptor agonists, whereas their counterpart 87 (R=Me) is a partialagonist. The cycloheptarenes 102-104 and 114-116 are all antagonists in the Xenopus model, whereas their benzocycloheptene congeners are either pure agonists (96-98) or pure antagonists (compounds 111-113).All new compounds possess stereoelectronic features, which enable them to act as agonist-partial agonist-antagonist molecular probe ―switches‖. An extension of the present thesis could involve the enantioselective synthesis of the most active racemic cyclobuta- and cycloheptarenes.

Subjects/Keywords: Αρωματικές ετεροκυκλικές ενώσεις; Αρωματικές καρβοκυκλικές ενώσεις; Μελατονινεργική δράση; Aromatic heterocycles compounds; Aromatic carbocycles compounds; Melatoninergic activity; Xenopus laevis

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APA (6^th Edition):

Αφρουδάκης, . �. (2011). Σχεδιασμός και σύνθεση νέων ετεροκυκλικών και καρβοκυκλικών ενώσεων με μελατονινεργική δράση. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/35232

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

Chicago Manual of Style (16^th Edition):

Αφρουδάκης, Παντελεήμων. “Σχεδιασμός και σύνθεση νέων ετεροκυκλικών και καρβοκυκλικών ενώσεων με μελατονινεργική δράση.” 2011. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed January 20, 2021. http://hdl.handle.net/10442/hedi/35232.

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

MLA Handbook (7^th Edition):

Αφρουδάκης, Παντελεήμων. “Σχεδιασμός και σύνθεση νέων ετεροκυκλικών και καρβοκυκλικών ενώσεων με μελατονινεργική δράση.” 2011. Web. 20 Jan 2021.

Vancouver:

Αφρουδάκης �. Σχεδιασμός και σύνθεση νέων ετεροκυκλικών και καρβοκυκλικών ενώσεων με μελατονινεργική δράση. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2011. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10442/hedi/35232.

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

Council of Science Editors:

Αφρουδάκης �. Σχεδιασμός και σύνθεση νέων ετεροκυκλικών και καρβοκυκλικών ενώσεων με μελατονινεργική δράση. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2011. Available from: http://hdl.handle.net/10442/hedi/35232

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

13. Gupta, Arun Kumar. Investigations on oxoketene dithioacetals : new carbon_carbon bond forming reactions and their further transformations to novel carbocycles and heterocycles; -.

Degree: Chemistry, 1989, North-Eastern Hill University

URL: http://shodhganga.inflibnet.ac.in/handle/10603/54747

Abstract not available newline newline

-

Advisors/Committee Members: Ila, H.

Subjects/Keywords: Oxoketene Dithioacetals; New Carbon_Carbon Bond Forming Reactions; Transformations; Novel Carbocycles; Heterocycles

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APA (6^th Edition):

Gupta, A. K. (1989). Investigations on oxoketene dithioacetals : new carbon_carbon bond forming reactions and their further transformations to novel carbocycles and heterocycles; -. (Thesis). North-Eastern Hill University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/54747

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

Chicago Manual of Style (16^th Edition):

Gupta, Arun Kumar. “Investigations on oxoketene dithioacetals : new carbon_carbon bond forming reactions and their further transformations to novel carbocycles and heterocycles; -.” 1989. Thesis, North-Eastern Hill University. Accessed January 20, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/54747.

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

MLA Handbook (7^th Edition):

Gupta, Arun Kumar. “Investigations on oxoketene dithioacetals : new carbon_carbon bond forming reactions and their further transformations to novel carbocycles and heterocycles; -.” 1989. Web. 20 Jan 2021.

Vancouver:

Gupta AK. Investigations on oxoketene dithioacetals : new carbon_carbon bond forming reactions and their further transformations to novel carbocycles and heterocycles; -. [Internet] [Thesis]. North-Eastern Hill University; 1989. [cited 2021 Jan 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54747.

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

Council of Science Editors:

Gupta AK. Investigations on oxoketene dithioacetals : new carbon_carbon bond forming reactions and their further transformations to novel carbocycles and heterocycles; -. [Thesis]. North-Eastern Hill University; 1989. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54747

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

14. Balu, M P. Synthetic investigations on polarized ketene dithioacetals: novel methods for the synthesis of carbocycles and heterocycles; -.

Degree: Chemistry, 1989, North-Eastern Hill University

URL: http://shodhganga.inflibnet.ac.in/handle/10603/54767

Abstract available newline newline

-

Advisors/Committee Members: Junjappa, H.

Subjects/Keywords: Synthetic Investigations; Polarized Ketene Dithioacetals; Novel Methods; Synthesis; Carbocycles; Heterocycles

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

APA (6^th Edition):

Balu, M. P. (1989). Synthetic investigations on polarized ketene dithioacetals: novel methods for the synthesis of carbocycles and heterocycles; -. (Thesis). North-Eastern Hill University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/54767

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

Chicago Manual of Style (16^th Edition):

Balu, M P. “Synthetic investigations on polarized ketene dithioacetals: novel methods for the synthesis of carbocycles and heterocycles; -.” 1989. Thesis, North-Eastern Hill University. Accessed January 20, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/54767.

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

MLA Handbook (7^th Edition):

Balu, M P. “Synthetic investigations on polarized ketene dithioacetals: novel methods for the synthesis of carbocycles and heterocycles; -.” 1989. Web. 20 Jan 2021.

Vancouver:

Balu MP. Synthetic investigations on polarized ketene dithioacetals: novel methods for the synthesis of carbocycles and heterocycles; -. [Internet] [Thesis]. North-Eastern Hill University; 1989. [cited 2021 Jan 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54767.

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

Council of Science Editors:

Balu MP. Synthetic investigations on polarized ketene dithioacetals: novel methods for the synthesis of carbocycles and heterocycles; -. [Thesis]. North-Eastern Hill University; 1989. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54767

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

15. Phun, Lien Hoang. Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles.

Degree: PhD, Chemistry and Biochemistry, 2013, Georgia Tech

URL: http://hdl.handle.net/1853/47542

► Natural products and small molecules play a major role in drug development. However, using natural products as a source of medicine comes with many challenges,… (more)

Subjects/Keywords: Furans; Carbocycles; Heterocycles; Cyclopropane; Cyclopropene; Diazo; Drug development; Pharmacognosy

…strained carbocycles led us to examine cyclopropene-3,3’-dicarbonyls as the reactive subunit… …carbocycles as the reactive subunit. In this thesis, new synthetic methodologies using cyclopropanes…

2 more images…

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

APA (6^th Edition):

Phun, L. H. (2013). Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/47542

Chicago Manual of Style (16^th Edition):

Phun, Lien Hoang. “Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles.” 2013. Doctoral Dissertation, Georgia Tech. Accessed January 20, 2021. http://hdl.handle.net/1853/47542.

MLA Handbook (7^th Edition):

Phun, Lien Hoang. “Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles.” 2013. Web. 20 Jan 2021.

Vancouver:

Phun LH. Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1853/47542.

Council of Science Editors:

Phun LH. Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/47542

16. Barabe, Francis. Gold(I)-Catalyzed Synthesis of Polycyclic Frameworks Related to Terpenes: Selective Divergent Synthesis of Fused Carbocycles .

Degree: 2013, University of Ottawa

URL: http://hdl.handle.net/10393/29055

► Gold catalysis has become an important tool to achieve highly chemoselective p-acid activation. Exceptional reactivity and selectivity are often encountered under mild reaction conditions. These… (more)

▼ Gold catalysis has become an important tool to achieve highly chemoselective p-acid activation. Exceptional reactivity and selectivity are often encountered under mild reaction conditions. These properties have made gold(I) complexes suitable catalysts for tremendous applications in the total synthesis of natural products. The first chapter will highlight a number of total syntheses using gold catalysis as a key step. The second chapter will cover our application of the gold(I)-catalyzed 6-endo-dig carbocyclization for the synthesis of bridgehead-substituted scaffolds and its use toward the synthesis of PPAP natural products. This research has opened our eyes to the utility of biphenylphosphine ligands, particularly JohnPhos, in gold(I)-catalysis. The reactivity and selectivity exhibited by gold(I) complexes is modulated by the nature of the ancillary ligand. Recent research rationalizes the impact of these ligands on the divergent reactivity observed between cationic and carbenoid intermediates. Our desire to favor the 6-endo-dig pathway has led us toward the discovery of another example of the diagonal reactivity that NHC carbene and biphenylphosphine ligands can bring to gold(I)-catalysis. Chapter three will explain the development of a selective gold-catalyzed synthesis of fused carbocycles . Our selective divergent synthesis of fused carbocycles, combined with the Diels–Alder reaction, has brought new synthetic opportunities. Chapter four will describe our approach toward the synthesis of various polycyclic diterpene-related frameworks. Starting with a unique linear precursor, we have developed a new “one-pot” process for the synthesis of three different polycyclic compounds related to the terpenoid family. The facile modulation of the linear precursor and the use of different dienophiles during the Diels–Alder reaction could enable the synthesis of diverse polycyclic analogues based on three principal frameworks. The gold(I)-catalyzed synthesis of fused carbocycles reached some limitations during our study. Regioselective control was found to be substantially more challenging, with terminal alkynes or alkynes bearing a sterically and electronically neutral methyl substituent. In chapter five, we will discuss how the complementarity of silver(I) catalysis to gold(I) catalysis enabled the selective divergent synthesis of three different fused carbocycles from a unique precursor. Moreover, copper(I) catalysis has given access to the 6-endo-dig pathway on terminal alkynes without the formation of a vinylidene intermediate.

Subjects/Keywords: gold(I)-catalysis; carbocyclization; fused carbocycles; bridged carbocycles; PPAP natural product; silver(I)-catalysis; copper(I)-catalysis; tandem reaction

…Selective Divergent Synthesis of Fused Carbocycles via a Gold(I)-Catalyzed… …fused carbocycles �� . ��...64 3.10 Scope of the selective gold… …gold(I)catalyzed synthesis of fused carbocycles �� …. ��….74 3.12 An… …limitation of the gold(I)-catalyzed synthesis of fused carbocycles…... ��…78 3.14… …x29;-catalysis �� …...110 5.2 Selective synthesis of fused carbocycles: methyl substituent…

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APA (6^th Edition):

Barabe, F. (2013). Gold(I)-Catalyzed Synthesis of Polycyclic Frameworks Related to Terpenes: Selective Divergent Synthesis of Fused Carbocycles . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/29055

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

Chicago Manual of Style (16^th Edition):

Barabe, Francis. “Gold(I)-Catalyzed Synthesis of Polycyclic Frameworks Related to Terpenes: Selective Divergent Synthesis of Fused Carbocycles .” 2013. Thesis, University of Ottawa. Accessed January 20, 2021. http://hdl.handle.net/10393/29055.

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

MLA Handbook (7^th Edition):

Barabe, Francis. “Gold(I)-Catalyzed Synthesis of Polycyclic Frameworks Related to Terpenes: Selective Divergent Synthesis of Fused Carbocycles .” 2013. Web. 20 Jan 2021.

Vancouver:

Barabe F. Gold(I)-Catalyzed Synthesis of Polycyclic Frameworks Related to Terpenes: Selective Divergent Synthesis of Fused Carbocycles . [Internet] [Thesis]. University of Ottawa; 2013. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10393/29055.

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

Council of Science Editors:

Barabe F. Gold(I)-Catalyzed Synthesis of Polycyclic Frameworks Related to Terpenes: Selective Divergent Synthesis of Fused Carbocycles . [Thesis]. University of Ottawa; 2013. Available from: http://hdl.handle.net/10393/29055

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

17. Bhaskar Kumar, T. Novel synthetic approaches towards heterocycles and carbocycles and their evaluation as potential inhibitors of pde4; -.

Degree: Chemistry, 2014, Jawaharlal Nehru Technological University, Anantapuram

URL: http://shodhganga.inflibnet.ac.in/handle/10603/26936

None

conclusion p.184-187, references p.188-208

Advisors/Committee Members: Chandra Sekhar, K B, Srinivasa Rao, M.

Subjects/Keywords: Chemistry; Potential inhibitors of PDE4; Synthetic approaches towards heterocycles and carbocycles and their evaluation

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APA (6^th Edition):

Bhaskar Kumar, T. (2014). Novel synthetic approaches towards heterocycles and carbocycles and their evaluation as potential inhibitors of pde4; -. (Thesis). Jawaharlal Nehru Technological University, Anantapuram. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/26936

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

Chicago Manual of Style (16^th Edition):

Bhaskar Kumar, T. “Novel synthetic approaches towards heterocycles and carbocycles and their evaluation as potential inhibitors of pde4; -.” 2014. Thesis, Jawaharlal Nehru Technological University, Anantapuram. Accessed January 20, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/26936.

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

MLA Handbook (7^th Edition):

Bhaskar Kumar, T. “Novel synthetic approaches towards heterocycles and carbocycles and their evaluation as potential inhibitors of pde4; -.” 2014. Web. 20 Jan 2021.

Vancouver:

Bhaskar Kumar T. Novel synthetic approaches towards heterocycles and carbocycles and their evaluation as potential inhibitors of pde4; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Anantapuram; 2014. [cited 2021 Jan 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26936.

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

Council of Science Editors:

Bhaskar Kumar T. Novel synthetic approaches towards heterocycles and carbocycles and their evaluation as potential inhibitors of pde4; -. [Thesis]. Jawaharlal Nehru Technological University, Anantapuram; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/26936

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

Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

18. Κόφτης, Θεοχάρης. Νέες μέθοδοι ενομοριακής κυκλοποίησης παράγωγων σακχάρων.

Degree: 2000, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

URL: http://hdl.handle.net/10442/hedi/25614

Subjects/Keywords: Υδατάνθρακες; Σάκχαρα; Καρβοκυκλικά; Εναμινόνες; Νιτριλοξείδια; Διαζωενώσεις; Κυκλοπροπανίωση; Κοντουριτόλες; Ολεφινική μετάθεση; Carbocycles; Enaminones; Nitrile oxides; Diazocompounds; Cyclopropanation; Conduritols; Olefin metathesis

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

APA (6^th Edition):

Κόφτης, . �. (2000). Νέες μέθοδοι ενομοριακής κυκλοποίησης παράγωγων σακχάρων. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/25614

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

Chicago Manual of Style (16^th Edition):

Κόφτης, Θεοχάρης. “Νέες μέθοδοι ενομοριακής κυκλοποίησης παράγωγων σακχάρων.” 2000. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed January 20, 2021. http://hdl.handle.net/10442/hedi/25614.

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

MLA Handbook (7^th Edition):

Κόφτης, Θεοχάρης. “Νέες μέθοδοι ενομοριακής κυκλοποίησης παράγωγων σακχάρων.” 2000. Web. 20 Jan 2021.

Vancouver:

Κόφτης �. Νέες μέθοδοι ενομοριακής κυκλοποίησης παράγωγων σακχάρων. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2000. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10442/hedi/25614.

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

Council of Science Editors:

Κόφτης �. Νέες μέθοδοι ενομοριακής κυκλοποίησης παράγωγων σακχάρων. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2000. Available from: http://hdl.handle.net/10442/hedi/25614

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

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Open Access Theses and Dissertations