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You searched for subject:(indole synthesis). Showing records 1 – 30 of 67 total matches.

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University of New South Wales

1. Chen, Rui. Synthesis of novel Indole-based Macrocycles.

Degree: Chemistry, 2012, University of New South Wales

 The formation of novel indolo-macrocyclic imines derived from N,N’-diindolylxylene dialdehydes has been investigated. The xylene linkage between two indole units was found to contribute to… (more)

Subjects/Keywords: Macrocycle; Indole; Biindolyl; Synthesis

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APA (6th Edition):

Chen, R. (2012). Synthesis of novel Indole-based Macrocycles. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52319 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10991/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Chen, Rui. “Synthesis of novel Indole-based Macrocycles.” 2012. Doctoral Dissertation, University of New South Wales. Accessed July 09, 2020. http://handle.unsw.edu.au/1959.4/52319 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10991/SOURCE01?view=true.

MLA Handbook (7th Edition):

Chen, Rui. “Synthesis of novel Indole-based Macrocycles.” 2012. Web. 09 Jul 2020.

Vancouver:

Chen R. Synthesis of novel Indole-based Macrocycles. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2020 Jul 09]. Available from: http://handle.unsw.edu.au/1959.4/52319 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10991/SOURCE01?view=true.

Council of Science Editors:

Chen R. Synthesis of novel Indole-based Macrocycles. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/52319 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10991/SOURCE01?view=true


University of New South Wales

2. Bingul, Murat. The synthesis and reactions of new activated indole derivatives.

Degree: Chemistry, 2010, University of New South Wales

 A range of methyl dimethoxyindole-2-carboxylate derivatives has successfully been prepared via the Hemetsberger reaction. The most reactive positions of the indole esters were formylated using… (more)

Subjects/Keywords: Reactions; Activated indole; Synthesis

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APA (6th Edition):

Bingul, M. (2010). The synthesis and reactions of new activated indole derivatives. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50121 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9039/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Bingul, Murat. “The synthesis and reactions of new activated indole derivatives.” 2010. Masters Thesis, University of New South Wales. Accessed July 09, 2020. http://handle.unsw.edu.au/1959.4/50121 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9039/SOURCE02?view=true.

MLA Handbook (7th Edition):

Bingul, Murat. “The synthesis and reactions of new activated indole derivatives.” 2010. Web. 09 Jul 2020.

Vancouver:

Bingul M. The synthesis and reactions of new activated indole derivatives. [Internet] [Masters thesis]. University of New South Wales; 2010. [cited 2020 Jul 09]. Available from: http://handle.unsw.edu.au/1959.4/50121 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9039/SOURCE02?view=true.

Council of Science Editors:

Bingul M. The synthesis and reactions of new activated indole derivatives. [Masters Thesis]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/50121 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9039/SOURCE02?view=true


University College Cork

3. Pierce, Laurence Thomas. Design, synthesis and development of novel indolocarbazole derivatives as potential anti-cancer agents.

Degree: 2011, University College Cork

 This thesis describes work carried out on the design of new routes to a range of bisindolylmaleimide and indolo[2,3-a]carbazole analogs, and investigation of their potential… (more)

Subjects/Keywords: Indolocarbazole; Indole; Carbazole; Cancer; Kinase; Indole – Synthesis; Indole – Therapeutic use; Cancer – Chemotherapy

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APA (6th Edition):

Pierce, L. T. (2011). Design, synthesis and development of novel indolocarbazole derivatives as potential anti-cancer agents. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/382

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):

Pierce, Laurence Thomas. “Design, synthesis and development of novel indolocarbazole derivatives as potential anti-cancer agents.” 2011. Thesis, University College Cork. Accessed July 09, 2020. http://hdl.handle.net/10468/382.

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

MLA Handbook (7th Edition):

Pierce, Laurence Thomas. “Design, synthesis and development of novel indolocarbazole derivatives as potential anti-cancer agents.” 2011. Web. 09 Jul 2020.

Vancouver:

Pierce LT. Design, synthesis and development of novel indolocarbazole derivatives as potential anti-cancer agents. [Internet] [Thesis]. University College Cork; 2011. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10468/382.

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

Council of Science Editors:

Pierce LT. Design, synthesis and development of novel indolocarbazole derivatives as potential anti-cancer agents. [Thesis]. University College Cork; 2011. Available from: http://hdl.handle.net/10468/382

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


Penn State University

4. Majireck, Max Michael. INTERMOLECULAR CONJUGATE ADDITION OF CARBON NUCLEOPHILES TO NITROSOALKENES AND STUDIES TOWARD A TOTAL SYNTHESIS OF.

Degree: PhD, Chemistry, 2011, Penn State University

 An efficient procedure for the alkylation of nitrosoalkenes has been developed in which an array of potassium ester enolates were found to add in Michael… (more)

Subjects/Keywords: indole; total synthesis; Michael addition; Nitrosoalkene; alkaloid

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APA (6th Edition):

Majireck, M. M. (2011). INTERMOLECULAR CONJUGATE ADDITION OF CARBON NUCLEOPHILES TO NITROSOALKENES AND STUDIES TOWARD A TOTAL SYNTHESIS OF. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/12036

Chicago Manual of Style (16th Edition):

Majireck, Max Michael. “INTERMOLECULAR CONJUGATE ADDITION OF CARBON NUCLEOPHILES TO NITROSOALKENES AND STUDIES TOWARD A TOTAL SYNTHESIS OF.” 2011. Doctoral Dissertation, Penn State University. Accessed July 09, 2020. https://etda.libraries.psu.edu/catalog/12036.

MLA Handbook (7th Edition):

Majireck, Max Michael. “INTERMOLECULAR CONJUGATE ADDITION OF CARBON NUCLEOPHILES TO NITROSOALKENES AND STUDIES TOWARD A TOTAL SYNTHESIS OF.” 2011. Web. 09 Jul 2020.

Vancouver:

Majireck MM. INTERMOLECULAR CONJUGATE ADDITION OF CARBON NUCLEOPHILES TO NITROSOALKENES AND STUDIES TOWARD A TOTAL SYNTHESIS OF. [Internet] [Doctoral dissertation]. Penn State University; 2011. [cited 2020 Jul 09]. Available from: https://etda.libraries.psu.edu/catalog/12036.

Council of Science Editors:

Majireck MM. INTERMOLECULAR CONJUGATE ADDITION OF CARBON NUCLEOPHILES TO NITROSOALKENES AND STUDIES TOWARD A TOTAL SYNTHESIS OF. [Doctoral Dissertation]. Penn State University; 2011. Available from: https://etda.libraries.psu.edu/catalog/12036

5. Prabhakar, K. Synthesis and Biological Evaluation of Indole and Thienopyrimidine Derivatives as 5-HT6 Receptor Ligands; -.

Degree: 2013, Jawaharlal Nehru Technological University, Hyderabad

The theme of the research work is design and synthesis of novel molecules which have potent affinity towards 5-HT 6 receptors. Based on this concept,… (more)

Subjects/Keywords: Biological; Derivatives; Evaluation; Indole; Synthesis; Thienopyrimidine

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APA (6th Edition):

Prabhakar, K. (2013). Synthesis and Biological Evaluation of Indole and Thienopyrimidine Derivatives as 5-HT6 Receptor Ligands; -. (Thesis). Jawaharlal Nehru Technological University, Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19552

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):

Prabhakar, K. “Synthesis and Biological Evaluation of Indole and Thienopyrimidine Derivatives as 5-HT6 Receptor Ligands; -.” 2013. Thesis, Jawaharlal Nehru Technological University, Hyderabad. Accessed July 09, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/19552.

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

MLA Handbook (7th Edition):

Prabhakar, K. “Synthesis and Biological Evaluation of Indole and Thienopyrimidine Derivatives as 5-HT6 Receptor Ligands; -.” 2013. Web. 09 Jul 2020.

Vancouver:

Prabhakar K. Synthesis and Biological Evaluation of Indole and Thienopyrimidine Derivatives as 5-HT6 Receptor Ligands; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. [cited 2020 Jul 09]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19552.

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

Council of Science Editors:

Prabhakar K. Synthesis and Biological Evaluation of Indole and Thienopyrimidine Derivatives as 5-HT6 Receptor Ligands; -. [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19552

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


University of Johannesburg

6. Greyling, Hendrik Frederik. Die sintese van alkaloiedagtige glikosidase-inhibeerders vanuit monosakkariede.

Degree: 2014, University of Johannesburg

M.Sc. (Chemistry)

The aim of this study was to investigate alternative routes for the stereocontrolled synthesis of hydroxylated indolizidine, piperidine and pyrrolidine alkaloids, starting from… (more)

Subjects/Keywords: Alkaloids - Synthesis; Indole alkaloids; Pyrrolidine; Piperidine

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APA (6th Edition):

Greyling, H. F. (2014). Die sintese van alkaloiedagtige glikosidase-inhibeerders vanuit monosakkariede. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/10917

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):

Greyling, Hendrik Frederik. “Die sintese van alkaloiedagtige glikosidase-inhibeerders vanuit monosakkariede.” 2014. Thesis, University of Johannesburg. Accessed July 09, 2020. http://hdl.handle.net/10210/10917.

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

MLA Handbook (7th Edition):

Greyling, Hendrik Frederik. “Die sintese van alkaloiedagtige glikosidase-inhibeerders vanuit monosakkariede.” 2014. Web. 09 Jul 2020.

Vancouver:

Greyling HF. Die sintese van alkaloiedagtige glikosidase-inhibeerders vanuit monosakkariede. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10210/10917.

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

Council of Science Editors:

Greyling HF. Die sintese van alkaloiedagtige glikosidase-inhibeerders vanuit monosakkariede. [Thesis]. University of Johannesburg; 2014. Available from: http://hdl.handle.net/10210/10917

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

7. CHADA, PHISALAPHONG. BIOMIMETIC SYNTHESIS OF INDOLE ALKALOIDS FROM AJMALINE.

Degree: Chiba University / 千葉大学

研究科: 千葉大学大学院薬学研究院

修了年:

学位:千大院薬博甲第73号

Advisors/Committee Members: 千葉大学大学院薬学研究院.

Subjects/Keywords: Indole Alkaloids; synthesis

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APA (6th Edition):

CHADA, P. (n.d.). BIOMIMETIC SYNTHESIS OF INDOLE ALKALOIDS FROM AJMALINE. (Thesis). Chiba University / 千葉大学. Retrieved from http://opac.ll.chiba-u.jp/da/curator/900047107/

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

CHADA, PHISALAPHONG. “BIOMIMETIC SYNTHESIS OF INDOLE ALKALOIDS FROM AJMALINE.” Thesis, Chiba University / 千葉大学. Accessed July 09, 2020. http://opac.ll.chiba-u.jp/da/curator/900047107/.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

CHADA, PHISALAPHONG. “BIOMIMETIC SYNTHESIS OF INDOLE ALKALOIDS FROM AJMALINE.” Web. 09 Jul 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

CHADA P. BIOMIMETIC SYNTHESIS OF INDOLE ALKALOIDS FROM AJMALINE. [Internet] [Thesis]. Chiba University / 千葉大学; [cited 2020 Jul 09]. Available from: http://opac.ll.chiba-u.jp/da/curator/900047107/.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

CHADA P. BIOMIMETIC SYNTHESIS OF INDOLE ALKALOIDS FROM AJMALINE. [Thesis]. Chiba University / 千葉大学; Available from: http://opac.ll.chiba-u.jp/da/curator/900047107/

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Oregon State University

8. Choi, Younggi. Total synthesis of indole alkaloids: pt. 1. Asymmetric synthesis of (-)-ibogamine. pt. 2. An approach toward the synthesis of koumine.

Degree: PhD, Chemistry, 2003, Oregon State University

 PART I. The preparation of (-)-ibogamine (1) in fourteen steps from benzoquinone and in 10% overall yield is a powerful illustration of the value of… (more)

Subjects/Keywords: Indole alkaloids  – Synthesis

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APA (6th Edition):

Choi, Y. (2003). Total synthesis of indole alkaloids: pt. 1. Asymmetric synthesis of (-)-ibogamine. pt. 2. An approach toward the synthesis of koumine. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/31054

Chicago Manual of Style (16th Edition):

Choi, Younggi. “Total synthesis of indole alkaloids: pt. 1. Asymmetric synthesis of (-)-ibogamine. pt. 2. An approach toward the synthesis of koumine.” 2003. Doctoral Dissertation, Oregon State University. Accessed July 09, 2020. http://hdl.handle.net/1957/31054.

MLA Handbook (7th Edition):

Choi, Younggi. “Total synthesis of indole alkaloids: pt. 1. Asymmetric synthesis of (-)-ibogamine. pt. 2. An approach toward the synthesis of koumine.” 2003. Web. 09 Jul 2020.

Vancouver:

Choi Y. Total synthesis of indole alkaloids: pt. 1. Asymmetric synthesis of (-)-ibogamine. pt. 2. An approach toward the synthesis of koumine. [Internet] [Doctoral dissertation]. Oregon State University; 2003. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/1957/31054.

Council of Science Editors:

Choi Y. Total synthesis of indole alkaloids: pt. 1. Asymmetric synthesis of (-)-ibogamine. pt. 2. An approach toward the synthesis of koumine. [Doctoral Dissertation]. Oregon State University; 2003. Available from: http://hdl.handle.net/1957/31054


Oregon State University

9. Ma, Yuelong. Synthetic studies on indolic enamide natural products: 1. Total syntheses of coscinamide A, concinamide B and igzamide: 2. Synthetic studies towards the synthesis of halocyamine B.

Degree: MS, Chemistry, 2006, Oregon State University

 The 3-substituded indolic enamide moiety has been found in many marine compounds over the past 20 years. These indolic enamides exhibit various biological properties such… (more)

Subjects/Keywords: Indole alkaloids  – Synthesis

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APA (6th Edition):

Ma, Y. (2006). Synthetic studies on indolic enamide natural products: 1. Total syntheses of coscinamide A, concinamide B and igzamide: 2. Synthetic studies towards the synthesis of halocyamine B. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/22508

Chicago Manual of Style (16th Edition):

Ma, Yuelong. “Synthetic studies on indolic enamide natural products: 1. Total syntheses of coscinamide A, concinamide B and igzamide: 2. Synthetic studies towards the synthesis of halocyamine B.” 2006. Masters Thesis, Oregon State University. Accessed July 09, 2020. http://hdl.handle.net/1957/22508.

MLA Handbook (7th Edition):

Ma, Yuelong. “Synthetic studies on indolic enamide natural products: 1. Total syntheses of coscinamide A, concinamide B and igzamide: 2. Synthetic studies towards the synthesis of halocyamine B.” 2006. Web. 09 Jul 2020.

Vancouver:

Ma Y. Synthetic studies on indolic enamide natural products: 1. Total syntheses of coscinamide A, concinamide B and igzamide: 2. Synthetic studies towards the synthesis of halocyamine B. [Internet] [Masters thesis]. Oregon State University; 2006. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/1957/22508.

Council of Science Editors:

Ma Y. Synthetic studies on indolic enamide natural products: 1. Total syntheses of coscinamide A, concinamide B and igzamide: 2. Synthetic studies towards the synthesis of halocyamine B. [Masters Thesis]. Oregon State University; 2006. Available from: http://hdl.handle.net/1957/22508


University of Colorado

10. Xu, Wenqing. Gold Approach to Polycyclic Indole Alkaloids and Chemical Probes for Histone Demethylases.

Degree: PhD, Chemistry & Biochemistry, 2014, University of Colorado

  My research contains two divisions: The first one is to develop novel synthetic methods for polycyclic indole alkaloids, such as strictamine. As one of… (more)

Subjects/Keywords: Monoterpene Indole Alkaloids; Cyclization; Synthesis; Chemistry

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APA (6th Edition):

Xu, W. (2014). Gold Approach to Polycyclic Indole Alkaloids and Chemical Probes for Histone Demethylases. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/138

Chicago Manual of Style (16th Edition):

Xu, Wenqing. “Gold Approach to Polycyclic Indole Alkaloids and Chemical Probes for Histone Demethylases.” 2014. Doctoral Dissertation, University of Colorado. Accessed July 09, 2020. https://scholar.colorado.edu/chem_gradetds/138.

MLA Handbook (7th Edition):

Xu, Wenqing. “Gold Approach to Polycyclic Indole Alkaloids and Chemical Probes for Histone Demethylases.” 2014. Web. 09 Jul 2020.

Vancouver:

Xu W. Gold Approach to Polycyclic Indole Alkaloids and Chemical Probes for Histone Demethylases. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2020 Jul 09]. Available from: https://scholar.colorado.edu/chem_gradetds/138.

Council of Science Editors:

Xu W. Gold Approach to Polycyclic Indole Alkaloids and Chemical Probes for Histone Demethylases. [Doctoral Dissertation]. University of Colorado; 2014. Available from: https://scholar.colorado.edu/chem_gradetds/138


University of New South Wales

11. Sengul, Ibrahim Fazil. Synthesis of new heterocycle-linked BIS-indole systems.

Degree: Chemistry, 2011, University of New South Wales

 The primary aim of this project was to synthesize relatively large molecular structures derived from novel 2- and 3-indolyl compounds and to investigate their properties… (more)

Subjects/Keywords: BIS-indole system; heterocycle-linked; synthesis

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APA (6th Edition):

Sengul, I. F. (2011). Synthesis of new heterocycle-linked BIS-indole systems. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10251/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Sengul, Ibrahim Fazil. “Synthesis of new heterocycle-linked BIS-indole systems.” 2011. Doctoral Dissertation, University of New South Wales. Accessed July 09, 2020. http://handle.unsw.edu.au/1959.4/51584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10251/SOURCE02?view=true.

MLA Handbook (7th Edition):

Sengul, Ibrahim Fazil. “Synthesis of new heterocycle-linked BIS-indole systems.” 2011. Web. 09 Jul 2020.

Vancouver:

Sengul IF. Synthesis of new heterocycle-linked BIS-indole systems. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2020 Jul 09]. Available from: http://handle.unsw.edu.au/1959.4/51584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10251/SOURCE02?view=true.

Council of Science Editors:

Sengul IF. Synthesis of new heterocycle-linked BIS-indole systems. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51584 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10251/SOURCE02?view=true


University of Adelaide

12. Liljegren, David Roland. Synthetical experiments related to the indole alkaloids / by David Roland Liljegren.

Degree: 1962, University of Adelaide

Subjects/Keywords: Indole alkaloids Synthesis

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APA (6th Edition):

Liljegren, D. R. (1962). Synthetical experiments related to the indole alkaloids / by David Roland Liljegren. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/20162

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):

Liljegren, David Roland. “Synthetical experiments related to the indole alkaloids / by David Roland Liljegren.” 1962. Thesis, University of Adelaide. Accessed July 09, 2020. http://hdl.handle.net/2440/20162.

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

MLA Handbook (7th Edition):

Liljegren, David Roland. “Synthetical experiments related to the indole alkaloids / by David Roland Liljegren.” 1962. Web. 09 Jul 2020.

Vancouver:

Liljegren DR. Synthetical experiments related to the indole alkaloids / by David Roland Liljegren. [Internet] [Thesis]. University of Adelaide; 1962. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2440/20162.

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

Council of Science Editors:

Liljegren DR. Synthetical experiments related to the indole alkaloids / by David Roland Liljegren. [Thesis]. University of Adelaide; 1962. Available from: http://hdl.handle.net/2440/20162

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


University of Hong Kong

13. Lee, Victor. Synthetic study of seco-yuehchukene and inverto-yuehchukene.

Degree: 1987, University of Hong Kong

Subjects/Keywords: Indole alkaloids - Synthesis.

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APA (6th Edition):

Lee, V. (1987). Synthetic study of seco-yuehchukene and inverto-yuehchukene. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/32314

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):

Lee, Victor. “Synthetic study of seco-yuehchukene and inverto-yuehchukene.” 1987. Thesis, University of Hong Kong. Accessed July 09, 2020. http://hdl.handle.net/10722/32314.

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

MLA Handbook (7th Edition):

Lee, Victor. “Synthetic study of seco-yuehchukene and inverto-yuehchukene.” 1987. Web. 09 Jul 2020.

Vancouver:

Lee V. Synthetic study of seco-yuehchukene and inverto-yuehchukene. [Internet] [Thesis]. University of Hong Kong; 1987. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10722/32314.

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

Council of Science Editors:

Lee V. Synthetic study of seco-yuehchukene and inverto-yuehchukene. [Thesis]. University of Hong Kong; 1987. Available from: http://hdl.handle.net/10722/32314

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


University of Hong Kong

14. 黃子達. A general synthetic route to Yuehchukene analogues via 7alpha-methoxycarbonyl-9-methyl-6-oxo-5,6,6abeta,7betaB,8,10aB-hexahydroindeno [2,1-b] indole, and related studies on 1-methoxyindole.

Degree: 1992, University of Hong Kong

Subjects/Keywords: Indole alkaloids - Synthesis.

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APA (6th Edition):

黃子達. (1992). A general synthetic route to Yuehchukene analogues via 7alpha-methoxycarbonyl-9-methyl-6-oxo-5,6,6abeta,7betaB,8,10aB-hexahydroindeno [2,1-b] indole, and related studies on 1-methoxyindole. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/34656

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

Chicago Manual of Style (16th Edition):

黃子達. “A general synthetic route to Yuehchukene analogues via 7alpha-methoxycarbonyl-9-methyl-6-oxo-5,6,6abeta,7betaB,8,10aB-hexahydroindeno [2,1-b] indole, and related studies on 1-methoxyindole.” 1992. Thesis, University of Hong Kong. Accessed July 09, 2020. http://hdl.handle.net/10722/34656.

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

MLA Handbook (7th Edition):

黃子達. “A general synthetic route to Yuehchukene analogues via 7alpha-methoxycarbonyl-9-methyl-6-oxo-5,6,6abeta,7betaB,8,10aB-hexahydroindeno [2,1-b] indole, and related studies on 1-methoxyindole.” 1992. Web. 09 Jul 2020.

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

Vancouver:

黃子達. A general synthetic route to Yuehchukene analogues via 7alpha-methoxycarbonyl-9-methyl-6-oxo-5,6,6abeta,7betaB,8,10aB-hexahydroindeno [2,1-b] indole, and related studies on 1-methoxyindole. [Internet] [Thesis]. University of Hong Kong; 1992. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10722/34656.

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

Council of Science Editors:

黃子達. A general synthetic route to Yuehchukene analogues via 7alpha-methoxycarbonyl-9-methyl-6-oxo-5,6,6abeta,7betaB,8,10aB-hexahydroindeno [2,1-b] indole, and related studies on 1-methoxyindole. [Thesis]. University of Hong Kong; 1992. Available from: http://hdl.handle.net/10722/34656

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


University of Hong Kong

15. Cheung, Man-ki. Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole.

Degree: 1995, University of Hong Kong

Subjects/Keywords: Indole alkaloids - Synthesis.

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APA (6th Edition):

Cheung, M. (1995). Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/35207

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):

Cheung, Man-ki. “Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole.” 1995. Thesis, University of Hong Kong. Accessed July 09, 2020. http://hdl.handle.net/10722/35207.

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

MLA Handbook (7th Edition):

Cheung, Man-ki. “Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole.” 1995. Web. 09 Jul 2020.

Vancouver:

Cheung M. Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. [Internet] [Thesis]. University of Hong Kong; 1995. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10722/35207.

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

Council of Science Editors:

Cheung M. Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. [Thesis]. University of Hong Kong; 1995. Available from: http://hdl.handle.net/10722/35207

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


University of St Andrews

16. Johnston, Craig A. Progress towards the synthesis of perophoramidine : formation of the contiguous quaternary centres.

Degree: PhD, 2013, University of St Andrews

 Perophoramidine 1 is a halogenated natural product which contains two contiguous quaternary centres within its structure. In this thesis, approaches towards the synthesis of perophoramidine… (more)

Subjects/Keywords: 547; Natural product synthesis; Perophoramidine; QP801.I45J7; Indole alkaloids – Synthesis

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APA (6th Edition):

Johnston, C. A. (2013). Progress towards the synthesis of perophoramidine : formation of the contiguous quaternary centres. (Doctoral Dissertation). University of St Andrews. Retrieved from http://hdl.handle.net/10023/3546

Chicago Manual of Style (16th Edition):

Johnston, Craig A. “Progress towards the synthesis of perophoramidine : formation of the contiguous quaternary centres.” 2013. Doctoral Dissertation, University of St Andrews. Accessed July 09, 2020. http://hdl.handle.net/10023/3546.

MLA Handbook (7th Edition):

Johnston, Craig A. “Progress towards the synthesis of perophoramidine : formation of the contiguous quaternary centres.” 2013. Web. 09 Jul 2020.

Vancouver:

Johnston CA. Progress towards the synthesis of perophoramidine : formation of the contiguous quaternary centres. [Internet] [Doctoral dissertation]. University of St Andrews; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10023/3546.

Council of Science Editors:

Johnston CA. Progress towards the synthesis of perophoramidine : formation of the contiguous quaternary centres. [Doctoral Dissertation]. University of St Andrews; 2013. Available from: http://hdl.handle.net/10023/3546


Dalhousie University

17. Alsabeh, Pamela G. The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions.

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

 The use of homogeneous organometallic catalysis for otherwise challenging chemical transformations is a concept that has gained significant interest in recent decades, providing access to… (more)

Subjects/Keywords: catalysis; cross-coupling; palladium; ammonia; amination; carbonylation; indole synthesis

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APA (6th Edition):

Alsabeh, P. G. (2013). The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/39740

Chicago Manual of Style (16th Edition):

Alsabeh, Pamela G. “The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions.” 2013. Doctoral Dissertation, Dalhousie University. Accessed July 09, 2020. http://hdl.handle.net/10222/39740.

MLA Handbook (7th Edition):

Alsabeh, Pamela G. “The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions.” 2013. Web. 09 Jul 2020.

Vancouver:

Alsabeh PG. The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions. [Internet] [Doctoral dissertation]. Dalhousie University; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10222/39740.

Council of Science Editors:

Alsabeh PG. The Development of Catalysts for the Monoarylation of Ammonia and Related Challenging Cross-Coupling Reactions. [Doctoral Dissertation]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/39740


Penn State University

18. Chauhan, Pradeep Singh. Part I - Synthesis of the Tetracyclic Skeleton of the Lycopodium Alkaloid Lycopladine H.

Degree: PhD, Chemistry, 2015, Penn State University

 Abstract Part I A synthesis of the tetracyclic framework 220 of the structurally unique Lycopodium alkaloid lycopladine H (21) has been achieved in 19 steps… (more)

Subjects/Keywords: synthesis; lycopodium; alkaloids; apparicine; nitrosoalkene; hydroformylation; indole; chlorooxime; dialdehyde; dialkene

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APA (6th Edition):

Chauhan, P. S. (2015). Part I - Synthesis of the Tetracyclic Skeleton of the Lycopodium Alkaloid Lycopladine H. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/23929

Chicago Manual of Style (16th Edition):

Chauhan, Pradeep Singh. “Part I - Synthesis of the Tetracyclic Skeleton of the Lycopodium Alkaloid Lycopladine H.” 2015. Doctoral Dissertation, Penn State University. Accessed July 09, 2020. https://etda.libraries.psu.edu/catalog/23929.

MLA Handbook (7th Edition):

Chauhan, Pradeep Singh. “Part I - Synthesis of the Tetracyclic Skeleton of the Lycopodium Alkaloid Lycopladine H.” 2015. Web. 09 Jul 2020.

Vancouver:

Chauhan PS. Part I - Synthesis of the Tetracyclic Skeleton of the Lycopodium Alkaloid Lycopladine H. [Internet] [Doctoral dissertation]. Penn State University; 2015. [cited 2020 Jul 09]. Available from: https://etda.libraries.psu.edu/catalog/23929.

Council of Science Editors:

Chauhan PS. Part I - Synthesis of the Tetracyclic Skeleton of the Lycopodium Alkaloid Lycopladine H. [Doctoral Dissertation]. Penn State University; 2015. Available from: https://etda.libraries.psu.edu/catalog/23929


Penn State University

19. Folda, Tamara Sandra. Progress Towards the Total Synthesis of (-)-gilbertine.

Degree: PhD, Chemistry, 2015, Penn State University

 This dissertation focuses on an allenyl azide cyclization approach towards (-)-gilbertine (4), a pentacyclic indole alkaloid that is part of the uleine family of natural… (more)

Subjects/Keywords: gilbertine; total synthesis; allenyl azide; cyclization cascade; photochemistry; indole alkaloid; organic

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APA (6th Edition):

Folda, T. S. (2015). Progress Towards the Total Synthesis of (-)-gilbertine. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/27568

Chicago Manual of Style (16th Edition):

Folda, Tamara Sandra. “Progress Towards the Total Synthesis of (-)-gilbertine.” 2015. Doctoral Dissertation, Penn State University. Accessed July 09, 2020. https://etda.libraries.psu.edu/catalog/27568.

MLA Handbook (7th Edition):

Folda, Tamara Sandra. “Progress Towards the Total Synthesis of (-)-gilbertine.” 2015. Web. 09 Jul 2020.

Vancouver:

Folda TS. Progress Towards the Total Synthesis of (-)-gilbertine. [Internet] [Doctoral dissertation]. Penn State University; 2015. [cited 2020 Jul 09]. Available from: https://etda.libraries.psu.edu/catalog/27568.

Council of Science Editors:

Folda TS. Progress Towards the Total Synthesis of (-)-gilbertine. [Doctoral Dissertation]. Penn State University; 2015. Available from: https://etda.libraries.psu.edu/catalog/27568


University of California – Berkeley

20. Mercado-Marin, Eduardo Valentin. A Unified Approach Toward the Total Syntheses of Prenylated Indole Alkaloid Natural Products.

Degree: Chemistry, 2016, University of California – Berkeley

 AbstractA Unified Approach Toward the Total Syntheses ofPrenylated Indole Alkaloid Natural ProductsbyEduardo Valentin Mercado-MarinDoctor of Philosophy in ChemistryUniversity of California, BerkeleyProfessor Richmond Sarpong, Chair This… (more)

Subjects/Keywords: Chemistry; citrinalins; cyclopiamines; prenylated indole alkaloids; stephacidins; Total synthesis

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APA (6th Edition):

Mercado-Marin, E. V. (2016). A Unified Approach Toward the Total Syntheses of Prenylated Indole Alkaloid Natural Products. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4th3q0hq

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):

Mercado-Marin, Eduardo Valentin. “A Unified Approach Toward the Total Syntheses of Prenylated Indole Alkaloid Natural Products.” 2016. Thesis, University of California – Berkeley. Accessed July 09, 2020. http://www.escholarship.org/uc/item/4th3q0hq.

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

MLA Handbook (7th Edition):

Mercado-Marin, Eduardo Valentin. “A Unified Approach Toward the Total Syntheses of Prenylated Indole Alkaloid Natural Products.” 2016. Web. 09 Jul 2020.

Vancouver:

Mercado-Marin EV. A Unified Approach Toward the Total Syntheses of Prenylated Indole Alkaloid Natural Products. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Jul 09]. Available from: http://www.escholarship.org/uc/item/4th3q0hq.

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

Council of Science Editors:

Mercado-Marin EV. A Unified Approach Toward the Total Syntheses of Prenylated Indole Alkaloid Natural Products. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/4th3q0hq

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


University of California – Berkeley

21. Zeldin, Rachel Motove. Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C.

Degree: Chemistry, 2011, University of California – Berkeley

 The modern era of synthetic chemistry can be characterized by increased understanding, development and application of transition metal complexes to traditionally organic transformations. While the… (more)

Subjects/Keywords: Chemistry; allenes; flinderole; gold; indole alkaloids; organometallic chemistry; total synthesis

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APA (6th Edition):

Zeldin, R. M. (2011). Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/5437m7h3

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):

Zeldin, Rachel Motove. “Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C.” 2011. Thesis, University of California – Berkeley. Accessed July 09, 2020. http://www.escholarship.org/uc/item/5437m7h3.

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

MLA Handbook (7th Edition):

Zeldin, Rachel Motove. “Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C.” 2011. Web. 09 Jul 2020.

Vancouver:

Zeldin RM. Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2020 Jul 09]. Available from: http://www.escholarship.org/uc/item/5437m7h3.

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

Council of Science Editors:

Zeldin RM. Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/5437m7h3

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

22. Sandhya, P V. Synthesis Characterization and application of indole based arylamines as hole transporting materials in solid state organic solar cells; -.

Degree: Chemical Science, 2014, Kannur University

None

References p. 168-179

Advisors/Committee Members: Haridas, K R.

Subjects/Keywords: Application; Arylamines; characterization; Indole; Synthesis

Page 1

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APA (6th Edition):

Sandhya, P. V. (2014). Synthesis Characterization and application of indole based arylamines as hole transporting materials in solid state organic solar cells; -. (Thesis). Kannur University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/29152

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):

Sandhya, P V. “Synthesis Characterization and application of indole based arylamines as hole transporting materials in solid state organic solar cells; -.” 2014. Thesis, Kannur University. Accessed July 09, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/29152.

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

MLA Handbook (7th Edition):

Sandhya, P V. “Synthesis Characterization and application of indole based arylamines as hole transporting materials in solid state organic solar cells; -.” 2014. Web. 09 Jul 2020.

Vancouver:

Sandhya PV. Synthesis Characterization and application of indole based arylamines as hole transporting materials in solid state organic solar cells; -. [Internet] [Thesis]. Kannur University; 2014. [cited 2020 Jul 09]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29152.

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

Council of Science Editors:

Sandhya PV. Synthesis Characterization and application of indole based arylamines as hole transporting materials in solid state organic solar cells; -. [Thesis]. Kannur University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29152

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


University of New South Wales

23. Alamgir, Mahiuddin. Synthesis and reactivity of some activated heterocyclic compounds.

Degree: Chemistry, 2007, University of New South Wales

 An alternate approach to the synthesis of calix[3]indoles has been demonstrated, but further attempted synthetic approaches to calixindoles using new leaving groups led to uncharacterized… (more)

Subjects/Keywords: Heterocyclic compounds  – Synthesis; Indole; Benzimidazoles

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APA (6th Edition):

Alamgir, M. (2007). Synthesis and reactivity of some activated heterocyclic compounds. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/40831 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1286/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Alamgir, Mahiuddin. “Synthesis and reactivity of some activated heterocyclic compounds.” 2007. Doctoral Dissertation, University of New South Wales. Accessed July 09, 2020. http://handle.unsw.edu.au/1959.4/40831 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1286/SOURCE02?view=true.

MLA Handbook (7th Edition):

Alamgir, Mahiuddin. “Synthesis and reactivity of some activated heterocyclic compounds.” 2007. Web. 09 Jul 2020.

Vancouver:

Alamgir M. Synthesis and reactivity of some activated heterocyclic compounds. [Internet] [Doctoral dissertation]. University of New South Wales; 2007. [cited 2020 Jul 09]. Available from: http://handle.unsw.edu.au/1959.4/40831 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1286/SOURCE02?view=true.

Council of Science Editors:

Alamgir M. Synthesis and reactivity of some activated heterocyclic compounds. [Doctoral Dissertation]. University of New South Wales; 2007. Available from: http://handle.unsw.edu.au/1959.4/40831 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1286/SOURCE02?view=true


University of Southern California

24. Myslinska, Malgorzata. New organoboron based multicomponent methodologies for the synthesis of novel heterocycles.

Degree: PhD, Chemistry, 2011, University of Southern California

 This dissertation describes the development of new, efficient and facile synthetic methodologies for the practical synthesis of novel heterocycles and highly substituted amine derivatives.; Chapter… (more)

Subjects/Keywords: multicomponent reactions; indole synthesis; Petasis reaction; propargylamines; organotrifluoroborates

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APA (6th Edition):

Myslinska, M. (2011). New organoboron based multicomponent methodologies for the synthesis of novel heterocycles. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/277397/rec/4404

Chicago Manual of Style (16th Edition):

Myslinska, Malgorzata. “New organoboron based multicomponent methodologies for the synthesis of novel heterocycles.” 2011. Doctoral Dissertation, University of Southern California. Accessed July 09, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/277397/rec/4404.

MLA Handbook (7th Edition):

Myslinska, Malgorzata. “New organoboron based multicomponent methodologies for the synthesis of novel heterocycles.” 2011. Web. 09 Jul 2020.

Vancouver:

Myslinska M. New organoboron based multicomponent methodologies for the synthesis of novel heterocycles. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Jul 09]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/277397/rec/4404.

Council of Science Editors:

Myslinska M. New organoboron based multicomponent methodologies for the synthesis of novel heterocycles. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/277397/rec/4404


University of Hong Kong

25. 林淑媚. Studies on diazoketone rearrangements and application toward the synthesis of welwistatin.

Degree: 2013, University of Hong Kong

Subjects/Keywords: Indole alkaloids - Synthesis; Diazo compounds

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APA (6th Edition):

林淑媚. (2013). Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/196009

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

Chicago Manual of Style (16th Edition):

林淑媚. “Studies on diazoketone rearrangements and application toward the synthesis of welwistatin.” 2013. Thesis, University of Hong Kong. Accessed July 09, 2020. http://hdl.handle.net/10722/196009.

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

MLA Handbook (7th Edition):

林淑媚. “Studies on diazoketone rearrangements and application toward the synthesis of welwistatin.” 2013. Web. 09 Jul 2020.

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

Vancouver:

林淑媚. Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. [Internet] [Thesis]. University of Hong Kong; 2013. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10722/196009.

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

Council of Science Editors:

林淑媚. Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. [Thesis]. University of Hong Kong; 2013. Available from: http://hdl.handle.net/10722/196009

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


Northeastern University

26. Shaw, Sydney Elizabeth. The effect of light, jasmonate, and tissue organization on the expression of vindoline pathway genes in Catharanthus roseus.

Degree: MS, Department of Chemical Engineering, 2015, Northeastern University

 Catharanthus roseus is the sole source of the valuable terpenoid indole alkaloid (TIA) anti-cancer compounds vinblastine and vincristine. Because the biosynthesis of vinblastine and vincristine… (more)

Subjects/Keywords: jasmonate; vindoline; Indole alkaloids; Synthesis; Terpenes; Synthesis; Vinblastine; Synthesis; Organic compounds; Synthesis; Catharanthus roseus; Biosynthesis; Genetic transcription

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APA (6th Edition):

Shaw, S. E. (2015). The effect of light, jasmonate, and tissue organization on the expression of vindoline pathway genes in Catharanthus roseus. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20194181

Chicago Manual of Style (16th Edition):

Shaw, Sydney Elizabeth. “The effect of light, jasmonate, and tissue organization on the expression of vindoline pathway genes in Catharanthus roseus.” 2015. Masters Thesis, Northeastern University. Accessed July 09, 2020. http://hdl.handle.net/2047/D20194181.

MLA Handbook (7th Edition):

Shaw, Sydney Elizabeth. “The effect of light, jasmonate, and tissue organization on the expression of vindoline pathway genes in Catharanthus roseus.” 2015. Web. 09 Jul 2020.

Vancouver:

Shaw SE. The effect of light, jasmonate, and tissue organization on the expression of vindoline pathway genes in Catharanthus roseus. [Internet] [Masters thesis]. Northeastern University; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2047/D20194181.

Council of Science Editors:

Shaw SE. The effect of light, jasmonate, and tissue organization on the expression of vindoline pathway genes in Catharanthus roseus. [Masters Thesis]. Northeastern University; 2015. Available from: http://hdl.handle.net/2047/D20194181

27. Juen, Ludovic. Synthèse et évaluation biologique d'inhibiteurs de STAT5 dans le traitement des leucémies myéloïdes : Targeting STAT5 proteins in myeloid leukemias : chemical inhibitors synthesis and pharmacological evaluation.

Degree: Docteur es, Chimie organique, 2016, Université François-Rabelais de Tours

Les leucémies, syndromes myéloprolifératifs et myelodysplasiques sont la première cause de cancer chez l’enfant de moins de 15 ans. Les facteurs de transcription STAT5 ont… (more)

Subjects/Keywords: Leucémie myéloïde; STAT5; 4,4-diméthyl-1,2,3,4-tétrahydroquinoléine; Indole; Synthèse hétérocyclique; Myeloid leukemia; STAT5; 4,4-dimethyl-1,2,3,4-tetrahydroquinoline; Indole; Heterocyclic synthesis

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

APA (6th Edition):

Juen, L. (2016). Synthèse et évaluation biologique d'inhibiteurs de STAT5 dans le traitement des leucémies myéloïdes : Targeting STAT5 proteins in myeloid leukemias : chemical inhibitors synthesis and pharmacological evaluation. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2016TOUR3811

Chicago Manual of Style (16th Edition):

Juen, Ludovic. “Synthèse et évaluation biologique d'inhibiteurs de STAT5 dans le traitement des leucémies myéloïdes : Targeting STAT5 proteins in myeloid leukemias : chemical inhibitors synthesis and pharmacological evaluation.” 2016. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed July 09, 2020. http://www.theses.fr/2016TOUR3811.

MLA Handbook (7th Edition):

Juen, Ludovic. “Synthèse et évaluation biologique d'inhibiteurs de STAT5 dans le traitement des leucémies myéloïdes : Targeting STAT5 proteins in myeloid leukemias : chemical inhibitors synthesis and pharmacological evaluation.” 2016. Web. 09 Jul 2020.

Vancouver:

Juen L. Synthèse et évaluation biologique d'inhibiteurs de STAT5 dans le traitement des leucémies myéloïdes : Targeting STAT5 proteins in myeloid leukemias : chemical inhibitors synthesis and pharmacological evaluation. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2016. [cited 2020 Jul 09]. Available from: http://www.theses.fr/2016TOUR3811.

Council of Science Editors:

Juen L. Synthèse et évaluation biologique d'inhibiteurs de STAT5 dans le traitement des leucémies myéloïdes : Targeting STAT5 proteins in myeloid leukemias : chemical inhibitors synthesis and pharmacological evaluation. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2016. Available from: http://www.theses.fr/2016TOUR3811


University of Pennsylvania

28. Zou, Yike. Synthetic Study Of Structurally Complex Indole Terpenes Total Syntheses Of (─)-Nodulisporic Acid D And (─)-Nodulisporic Acid C In Conjunction With Advanced Synthetic Studies Towards (+)-Nodulisporic Acid A And (─)-Nodulisporic Acid B.

Degree: 2017, University of Pennsylvania

 The first total syntheses of architecturally complex indole terpenes (−)-nodulisporic acid D and (−)-nodulisporic acid C are reported here via a unified strategy of late-stage… (more)

Subjects/Keywords: cross coupling; indole; natural product; NODULISPORIC ACID; terpene; total synthesis; Chemistry; Organic Chemistry

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

APA (6th Edition):

Zou, Y. (2017). Synthetic Study Of Structurally Complex Indole Terpenes Total Syntheses Of (─)-Nodulisporic Acid D And (─)-Nodulisporic Acid C In Conjunction With Advanced Synthetic Studies Towards (+)-Nodulisporic Acid A And (─)-Nodulisporic Acid B. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2947

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):

Zou, Yike. “Synthetic Study Of Structurally Complex Indole Terpenes Total Syntheses Of (─)-Nodulisporic Acid D And (─)-Nodulisporic Acid C In Conjunction With Advanced Synthetic Studies Towards (+)-Nodulisporic Acid A And (─)-Nodulisporic Acid B.” 2017. Thesis, University of Pennsylvania. Accessed July 09, 2020. https://repository.upenn.edu/edissertations/2947.

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

MLA Handbook (7th Edition):

Zou, Yike. “Synthetic Study Of Structurally Complex Indole Terpenes Total Syntheses Of (─)-Nodulisporic Acid D And (─)-Nodulisporic Acid C In Conjunction With Advanced Synthetic Studies Towards (+)-Nodulisporic Acid A And (─)-Nodulisporic Acid B.” 2017. Web. 09 Jul 2020.

Vancouver:

Zou Y. Synthetic Study Of Structurally Complex Indole Terpenes Total Syntheses Of (─)-Nodulisporic Acid D And (─)-Nodulisporic Acid C In Conjunction With Advanced Synthetic Studies Towards (+)-Nodulisporic Acid A And (─)-Nodulisporic Acid B. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2020 Jul 09]. Available from: https://repository.upenn.edu/edissertations/2947.

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

Council of Science Editors:

Zou Y. Synthetic Study Of Structurally Complex Indole Terpenes Total Syntheses Of (─)-Nodulisporic Acid D And (─)-Nodulisporic Acid C In Conjunction With Advanced Synthetic Studies Towards (+)-Nodulisporic Acid A And (─)-Nodulisporic Acid B. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2947

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

29. Reyes Loya, David. Etude synthétique de la koumine, réactions domino régiosélectives vers des lactones indoliques et synthèse totale de la (+/-)-goniomithine. : Synthetic study of koumine, domino regioselective reactions towards indole lactones and total synthesis of (+/-)-goniomithine.

Degree: Docteur es, Chimie organique, 2017, Normandie

Une étude synthétique de la koumine par une stratégie basée sur une étape de désymétrisation a permis de développer, par un résultat inattendu, une fragmentation… (more)

Subjects/Keywords: Koumine; Régioséléctivité; Alcaloïdes indoliques; Goniomitine; Synthèse totale; Koumine; Regioselectivity; Indole alkaloids; Goniomitine; Total Synthesis; 547

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

APA (6th Edition):

Reyes Loya, D. (2017). Etude synthétique de la koumine, réactions domino régiosélectives vers des lactones indoliques et synthèse totale de la (+/-)-goniomithine. : Synthetic study of koumine, domino regioselective reactions towards indole lactones and total synthesis of (+/-)-goniomithine. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2017NORMR119

Chicago Manual of Style (16th Edition):

Reyes Loya, David. “Etude synthétique de la koumine, réactions domino régiosélectives vers des lactones indoliques et synthèse totale de la (+/-)-goniomithine. : Synthetic study of koumine, domino regioselective reactions towards indole lactones and total synthesis of (+/-)-goniomithine.” 2017. Doctoral Dissertation, Normandie. Accessed July 09, 2020. http://www.theses.fr/2017NORMR119.

MLA Handbook (7th Edition):

Reyes Loya, David. “Etude synthétique de la koumine, réactions domino régiosélectives vers des lactones indoliques et synthèse totale de la (+/-)-goniomithine. : Synthetic study of koumine, domino regioselective reactions towards indole lactones and total synthesis of (+/-)-goniomithine.” 2017. Web. 09 Jul 2020.

Vancouver:

Reyes Loya D. Etude synthétique de la koumine, réactions domino régiosélectives vers des lactones indoliques et synthèse totale de la (+/-)-goniomithine. : Synthetic study of koumine, domino regioselective reactions towards indole lactones and total synthesis of (+/-)-goniomithine. [Internet] [Doctoral dissertation]. Normandie; 2017. [cited 2020 Jul 09]. Available from: http://www.theses.fr/2017NORMR119.

Council of Science Editors:

Reyes Loya D. Etude synthétique de la koumine, réactions domino régiosélectives vers des lactones indoliques et synthèse totale de la (+/-)-goniomithine. : Synthetic study of koumine, domino regioselective reactions towards indole lactones and total synthesis of (+/-)-goniomithine. [Doctoral Dissertation]. Normandie; 2017. Available from: http://www.theses.fr/2017NORMR119


University of Hong Kong

30. 黃偉雄. Synthetic studies of N-benzenesulphonyl-6-oxo-5,6,8,9,10,10a-hexahydroindeno [2,1-b]indole and related compounds as intermediatesof C-7 substituted Yuehchukene analogues.

Degree: 1990, University of Hong Kong

Subjects/Keywords: Diels-Alder reaction.; Indole alkaloids - Synthesis.

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

APA (6th Edition):

黃偉雄. (1990). Synthetic studies of N-benzenesulphonyl-6-oxo-5,6,8,9,10,10a-hexahydroindeno [2,1-b]indole and related compounds as intermediatesof C-7 substituted Yuehchukene analogues. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/32356

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

Chicago Manual of Style (16th Edition):

黃偉雄. “Synthetic studies of N-benzenesulphonyl-6-oxo-5,6,8,9,10,10a-hexahydroindeno [2,1-b]indole and related compounds as intermediatesof C-7 substituted Yuehchukene analogues.” 1990. Thesis, University of Hong Kong. Accessed July 09, 2020. http://hdl.handle.net/10722/32356.

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

MLA Handbook (7th Edition):

黃偉雄. “Synthetic studies of N-benzenesulphonyl-6-oxo-5,6,8,9,10,10a-hexahydroindeno [2,1-b]indole and related compounds as intermediatesof C-7 substituted Yuehchukene analogues.” 1990. Web. 09 Jul 2020.

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

Vancouver:

黃偉雄. Synthetic studies of N-benzenesulphonyl-6-oxo-5,6,8,9,10,10a-hexahydroindeno [2,1-b]indole and related compounds as intermediatesof C-7 substituted Yuehchukene analogues. [Internet] [Thesis]. University of Hong Kong; 1990. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/10722/32356.

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

Council of Science Editors:

黃偉雄. Synthetic studies of N-benzenesulphonyl-6-oxo-5,6,8,9,10,10a-hexahydroindeno [2,1-b]indole and related compounds as intermediatesof C-7 substituted Yuehchukene analogues. [Thesis]. University of Hong Kong; 1990. Available from: http://hdl.handle.net/10722/32356

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

[1] [2] [3]

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