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You searched for subject:( monoterpene indole alkaloids). Showing records 1 – 30 of 1012 total matches.

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University of Colorado

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

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 http://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 May 22, 2019. http://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. 22 May 2019.

Vancouver:

Xu W. Gold Approach to Polycyclic Indole Alkaloids and Chemical Probes for Histone Demethylases. [Internet] [Doctoral dissertation]. University of Colorado; 2014. [cited 2019 May 22]. Available from: http://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: http://scholar.colorado.edu/chem_gradetds/138


Brock University

2. Woolfson, Kathlyn. Preliminary characterization of VmTPT2, a putative monoterpene indole alkaloid (MIA) transporter from Vinca minor L. (Apocynaceae) .

Degree: Department of Biological Sciences, 2014, Brock University

 The various steps of monoterpene indole alkaloid (MIA) biosynthesis are known to occur in specialized cell types and subcellular compartments. Numerous MIAs display powerful biological… (more)

Subjects/Keywords: ABC transporter; plant secondary metabolism; monoterpene indole alkaloids; Vinca minor; Apocynaceae

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APA (6th Edition):

Woolfson, K. (2014). Preliminary characterization of VmTPT2, a putative monoterpene indole alkaloid (MIA) transporter from Vinca minor L. (Apocynaceae) . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/5686

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):

Woolfson, Kathlyn. “Preliminary characterization of VmTPT2, a putative monoterpene indole alkaloid (MIA) transporter from Vinca minor L. (Apocynaceae) .” 2014. Thesis, Brock University. Accessed May 22, 2019. http://hdl.handle.net/10464/5686.

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

MLA Handbook (7th Edition):

Woolfson, Kathlyn. “Preliminary characterization of VmTPT2, a putative monoterpene indole alkaloid (MIA) transporter from Vinca minor L. (Apocynaceae) .” 2014. Web. 22 May 2019.

Vancouver:

Woolfson K. Preliminary characterization of VmTPT2, a putative monoterpene indole alkaloid (MIA) transporter from Vinca minor L. (Apocynaceae) . [Internet] [Thesis]. Brock University; 2014. [cited 2019 May 22]. Available from: http://hdl.handle.net/10464/5686.

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

Council of Science Editors:

Woolfson K. Preliminary characterization of VmTPT2, a putative monoterpene indole alkaloid (MIA) transporter from Vinca minor L. (Apocynaceae) . [Thesis]. Brock University; 2014. Available from: http://hdl.handle.net/10464/5686

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


Universidade do Rio Grande do Sul

3. Matsuura, Hélio Nitta. Papel do alcalóide N,B-D-glicopiranosil vincosamida na resposta a dano mecânico e herbivoria em Psychotria leiocarpa CHAM & SCHLTDL.

Degree: 2012, Universidade do Rio Grande do Sul

Metabólitos secundários são produzidos por alguns grupos vegetais e são essenciais nas diferentes estratégias de adaptação às adversidades ambientais, atuando na proteção e comunicação das… (more)

Subjects/Keywords: Monoterpene indole alkaloids; Alcaloide; UV-B radiation; Alcaloide; Fisiologia vegetal : Teses; Phytoanticipin; Antioxidant activity; Herbivory

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APA (6th Edition):

Matsuura, H. N. (2012). Papel do alcalóide N,B-D-glicopiranosil vincosamida na resposta a dano mecânico e herbivoria em Psychotria leiocarpa CHAM & SCHLTDL. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/143359

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):

Matsuura, Hélio Nitta. “Papel do alcalóide N,B-D-glicopiranosil vincosamida na resposta a dano mecânico e herbivoria em Psychotria leiocarpa CHAM & SCHLTDL.” 2012. Thesis, Universidade do Rio Grande do Sul. Accessed May 22, 2019. http://hdl.handle.net/10183/143359.

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

MLA Handbook (7th Edition):

Matsuura, Hélio Nitta. “Papel do alcalóide N,B-D-glicopiranosil vincosamida na resposta a dano mecânico e herbivoria em Psychotria leiocarpa CHAM & SCHLTDL.” 2012. Web. 22 May 2019.

Vancouver:

Matsuura HN. Papel do alcalóide N,B-D-glicopiranosil vincosamida na resposta a dano mecânico e herbivoria em Psychotria leiocarpa CHAM & SCHLTDL. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2012. [cited 2019 May 22]. Available from: http://hdl.handle.net/10183/143359.

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

Council of Science Editors:

Matsuura HN. Papel do alcalóide N,B-D-glicopiranosil vincosamida na resposta a dano mecânico e herbivoria em Psychotria leiocarpa CHAM & SCHLTDL. [Thesis]. Universidade do Rio Grande do Sul; 2012. Available from: http://hdl.handle.net/10183/143359

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


Georgia Tech

4. Ehrenworth, Amy M. Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae.

Degree: PhD, Chemistry and Biochemistry, 2017, Georgia Tech

Alkaloids are a large group of plant natural products that have important therapeutic value. Because of their chemical complexity, therapeutic alkaloids are often obtained via… (more)

Subjects/Keywords: Yeast; Saccharomyces cerevisiae; Alkaloids; Monoterpene indole alkaloids; Synthetic biology; Compartmentalization; Tetrahydrobiopterin; Natural product biosynthesis; Hydroxystrictosidine; Serotonin; Metabolic engineering; GPCR; Biosensor

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

APA (6th Edition):

Ehrenworth, A. M. (2017). Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60672

Chicago Manual of Style (16th Edition):

Ehrenworth, Amy M. “Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae.” 2017. Doctoral Dissertation, Georgia Tech. Accessed May 22, 2019. http://hdl.handle.net/1853/60672.

MLA Handbook (7th Edition):

Ehrenworth, Amy M. “Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae.” 2017. Web. 22 May 2019.

Vancouver:

Ehrenworth AM. Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 May 22]. Available from: http://hdl.handle.net/1853/60672.

Council of Science Editors:

Ehrenworth AM. Modified monoterpene indole alkaloid production in the yeast Saccharomyces cerevisiae. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60672

5. Otogo n'nang, Elvis. Étude chimique et biologique de Gentianales gabonaises d’intérêt antipaludique, à alcaloïdes indolomonoterpéniques : Chemical and biological study of Gabonese Gentianales with antoplasmodial interest, bearing monoterpene indole alkaloids.

Degree: Docteur es, Chimie des substances naturelles, 2018, Paris Saclay; Université des Sciences et Techniques de Masuku (Gabon)

L’étude chimique de 11 plantes du Gabon, dont certaines utilisées en médecine traditionnelle, a été réalisée à la recherche de composés antiplasmodiaux de structures nouvelles.… (more)

Subjects/Keywords: Alcaloïdes indolomonoterpéniques; Apocynaceae; Clhp-Ms/ms; Gelsemiacae; Réseaux moléculaires; Paludisme; Apocynaceae; Gelesemiaceae; Hplc-Ms/ms; Indole monoterpene alkaloids; Malaria; Molecular networking

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APA (6th Edition):

Otogo n'nang, E. (2018). Étude chimique et biologique de Gentianales gabonaises d’intérêt antipaludique, à alcaloïdes indolomonoterpéniques : Chemical and biological study of Gabonese Gentianales with antoplasmodial interest, bearing monoterpene indole alkaloids. (Doctoral Dissertation). Paris Saclay; Université des Sciences et Techniques de Masuku (Gabon). Retrieved from http://www.theses.fr/2018SACLS039

Chicago Manual of Style (16th Edition):

Otogo n'nang, Elvis. “Étude chimique et biologique de Gentianales gabonaises d’intérêt antipaludique, à alcaloïdes indolomonoterpéniques : Chemical and biological study of Gabonese Gentianales with antoplasmodial interest, bearing monoterpene indole alkaloids.” 2018. Doctoral Dissertation, Paris Saclay; Université des Sciences et Techniques de Masuku (Gabon). Accessed May 22, 2019. http://www.theses.fr/2018SACLS039.

MLA Handbook (7th Edition):

Otogo n'nang, Elvis. “Étude chimique et biologique de Gentianales gabonaises d’intérêt antipaludique, à alcaloïdes indolomonoterpéniques : Chemical and biological study of Gabonese Gentianales with antoplasmodial interest, bearing monoterpene indole alkaloids.” 2018. Web. 22 May 2019.

Vancouver:

Otogo n'nang E. Étude chimique et biologique de Gentianales gabonaises d’intérêt antipaludique, à alcaloïdes indolomonoterpéniques : Chemical and biological study of Gabonese Gentianales with antoplasmodial interest, bearing monoterpene indole alkaloids. [Internet] [Doctoral dissertation]. Paris Saclay; Université des Sciences et Techniques de Masuku (Gabon); 2018. [cited 2019 May 22]. Available from: http://www.theses.fr/2018SACLS039.

Council of Science Editors:

Otogo n'nang E. Étude chimique et biologique de Gentianales gabonaises d’intérêt antipaludique, à alcaloïdes indolomonoterpéniques : Chemical and biological study of Gabonese Gentianales with antoplasmodial interest, bearing monoterpene indole alkaloids. [Doctoral Dissertation]. Paris Saclay; Université des Sciences et Techniques de Masuku (Gabon); 2018. Available from: http://www.theses.fr/2018SACLS039

6. Fox ramos, Alexander. Exploration de la diversité chimique des Apocynaceae par la technique des réseaux moléculaires : de la création d’une base de données vers l’annotation in silico : Exploration of the chemical diversity of Apocynaceae plants using molecular networking : From the creation of a spectral database to in silico annotations.

Degree: Docteur es, Chimie des substances naturelles, 2018, Paris Saclay

Les alcaloïdes indolo-monoterpéniques (AIMs) constituent une classe de molécules naturelles très étudiée en raison d’un fort potentiel pharmacologique et thérapeutique et d’une grande diversité structurale.… (more)

Subjects/Keywords: Alcaloïdes indolomonoterpéniques; Apocynaceae; Base de données; Déréplication; Réseau moléculaire; Spectrométrie de masse; Apocynaceae; Database; Dereplication; Mass spectrometry; Molecular networking; Monoterpene indole alkaloids

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

APA (6th Edition):

Fox ramos, A. (2018). Exploration de la diversité chimique des Apocynaceae par la technique des réseaux moléculaires : de la création d’une base de données vers l’annotation in silico : Exploration of the chemical diversity of Apocynaceae plants using molecular networking : From the creation of a spectral database to in silico annotations. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS543

Chicago Manual of Style (16th Edition):

Fox ramos, Alexander. “Exploration de la diversité chimique des Apocynaceae par la technique des réseaux moléculaires : de la création d’une base de données vers l’annotation in silico : Exploration of the chemical diversity of Apocynaceae plants using molecular networking : From the creation of a spectral database to in silico annotations.” 2018. Doctoral Dissertation, Paris Saclay. Accessed May 22, 2019. http://www.theses.fr/2018SACLS543.

MLA Handbook (7th Edition):

Fox ramos, Alexander. “Exploration de la diversité chimique des Apocynaceae par la technique des réseaux moléculaires : de la création d’une base de données vers l’annotation in silico : Exploration of the chemical diversity of Apocynaceae plants using molecular networking : From the creation of a spectral database to in silico annotations.” 2018. Web. 22 May 2019.

Vancouver:

Fox ramos A. Exploration de la diversité chimique des Apocynaceae par la technique des réseaux moléculaires : de la création d’une base de données vers l’annotation in silico : Exploration of the chemical diversity of Apocynaceae plants using molecular networking : From the creation of a spectral database to in silico annotations. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 May 22]. Available from: http://www.theses.fr/2018SACLS543.

Council of Science Editors:

Fox ramos A. Exploration de la diversité chimique des Apocynaceae par la technique des réseaux moléculaires : de la création d’une base de données vers l’annotation in silico : Exploration of the chemical diversity of Apocynaceae plants using molecular networking : From the creation of a spectral database to in silico annotations. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS543


Oregon State University

7. Swanson, Hollie I. Effects of the anticarcinogen indole-3-carbinol on Xenobiotic metabolizing enzymes in rainbow trout.

Degree: MS, Food Science and Technology, 1988, Oregon State University

Indole-3-carbinol (I3C) inhibits chemically induced tumor formation in rodents and rainbow trout. This study examines the effect of I3C and its analog, indole-3-acetonitrile (I3N) on… (more)

Subjects/Keywords: Indole alkaloids

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APA (6th Edition):

Swanson, H. I. (1988). Effects of the anticarcinogen indole-3-carbinol on Xenobiotic metabolizing enzymes in rainbow trout. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/27196

Chicago Manual of Style (16th Edition):

Swanson, Hollie I. “Effects of the anticarcinogen indole-3-carbinol on Xenobiotic metabolizing enzymes in rainbow trout.” 1988. Masters Thesis, Oregon State University. Accessed May 22, 2019. http://hdl.handle.net/1957/27196.

MLA Handbook (7th Edition):

Swanson, Hollie I. “Effects of the anticarcinogen indole-3-carbinol on Xenobiotic metabolizing enzymes in rainbow trout.” 1988. Web. 22 May 2019.

Vancouver:

Swanson HI. Effects of the anticarcinogen indole-3-carbinol on Xenobiotic metabolizing enzymes in rainbow trout. [Internet] [Masters thesis]. Oregon State University; 1988. [cited 2019 May 22]. Available from: http://hdl.handle.net/1957/27196.

Council of Science Editors:

Swanson HI. Effects of the anticarcinogen indole-3-carbinol on Xenobiotic metabolizing enzymes in rainbow trout. [Masters Thesis]. Oregon State University; 1988. Available from: http://hdl.handle.net/1957/27196


University of British Columbia

8. De Souza, Joao Pedro. Synthetic studies in dihydroindole and indole alkaloids .

Degree: 1973, University of British Columbia

 A synthetic approach toward the synthesis of vindoline (3) and a reinvestigation of the total synthesis of vincaminoridine (4) and epivincaminoridine (4a) is described. The… (more)

Subjects/Keywords: Indole; Alkaloids

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APA (6th Edition):

De Souza, J. P. (1973). Synthetic studies in dihydroindole and indole alkaloids . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/19047

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):

De Souza, Joao Pedro. “Synthetic studies in dihydroindole and indole alkaloids .” 1973. Thesis, University of British Columbia. Accessed May 22, 2019. http://hdl.handle.net/2429/19047.

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

MLA Handbook (7th Edition):

De Souza, Joao Pedro. “Synthetic studies in dihydroindole and indole alkaloids .” 1973. Web. 22 May 2019.

Vancouver:

De Souza JP. Synthetic studies in dihydroindole and indole alkaloids . [Internet] [Thesis]. University of British Columbia; 1973. [cited 2019 May 22]. Available from: http://hdl.handle.net/2429/19047.

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

Council of Science Editors:

De Souza JP. Synthetic studies in dihydroindole and indole alkaloids . [Thesis]. University of British Columbia; 1973. Available from: http://hdl.handle.net/2429/19047

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


University of British Columbia

9. Fuller, George Bohn. Studies on the synthesis and biosynthesis of indole alkaloids .

Degree: 1974, University of British Columbia

 Part A of this thesis provides a resume1 of the synthesis of various radioactively labelled forms of secodine C76) and provides an evaluation of these… (more)

Subjects/Keywords: Indole alkaloids

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APA (6th Edition):

Fuller, G. B. (1974). Studies on the synthesis and biosynthesis of indole alkaloids . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/19051

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):

Fuller, George Bohn. “Studies on the synthesis and biosynthesis of indole alkaloids .” 1974. Thesis, University of British Columbia. Accessed May 22, 2019. http://hdl.handle.net/2429/19051.

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

MLA Handbook (7th Edition):

Fuller, George Bohn. “Studies on the synthesis and biosynthesis of indole alkaloids .” 1974. Web. 22 May 2019.

Vancouver:

Fuller GB. Studies on the synthesis and biosynthesis of indole alkaloids . [Internet] [Thesis]. University of British Columbia; 1974. [cited 2019 May 22]. Available from: http://hdl.handle.net/2429/19051.

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

Council of Science Editors:

Fuller GB. Studies on the synthesis and biosynthesis of indole alkaloids . [Thesis]. University of British Columbia; 1974. Available from: http://hdl.handle.net/2429/19051

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


University of British Columbia

10. Treasurywala, Adi Minoo. Studies related to the synthesis of bisindole alkaloids of the Indole-Indoline type .

Degree: 1974, University of British Columbia

 The first part of this thesis describes the synthesis of 3,4- functionalized cleavamine templates bearing a C₁₈- carbomethoxy group. Thus hydroboration of 18β-carbomethoxycleavamine (29) produced… (more)

Subjects/Keywords: Indole; Alkaloids

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APA (6th Edition):

Treasurywala, A. M. (1974). Studies related to the synthesis of bisindole alkaloids of the Indole-Indoline type . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/19195

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):

Treasurywala, Adi Minoo. “Studies related to the synthesis of bisindole alkaloids of the Indole-Indoline type .” 1974. Thesis, University of British Columbia. Accessed May 22, 2019. http://hdl.handle.net/2429/19195.

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

MLA Handbook (7th Edition):

Treasurywala, Adi Minoo. “Studies related to the synthesis of bisindole alkaloids of the Indole-Indoline type .” 1974. Web. 22 May 2019.

Vancouver:

Treasurywala AM. Studies related to the synthesis of bisindole alkaloids of the Indole-Indoline type . [Internet] [Thesis]. University of British Columbia; 1974. [cited 2019 May 22]. Available from: http://hdl.handle.net/2429/19195.

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

Council of Science Editors:

Treasurywala AM. Studies related to the synthesis of bisindole alkaloids of the Indole-Indoline type . [Thesis]. University of British Columbia; 1974. Available from: http://hdl.handle.net/2429/19195

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


University of British Columbia

11. Lewis, Norman G. Studies on the synthesis and biosynthesis of indole alkaloids .

Degree: 1978, University of British Columbia

 Part I of this thesis describes the more recent investigations towards the elucidation of the biosynthetic pathways leading to the formation of a class of… (more)

Subjects/Keywords: Indole alkaloids

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APA (6th Edition):

Lewis, N. G. (1978). Studies on the synthesis and biosynthesis of indole alkaloids . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/21626

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):

Lewis, Norman G. “Studies on the synthesis and biosynthesis of indole alkaloids .” 1978. Thesis, University of British Columbia. Accessed May 22, 2019. http://hdl.handle.net/2429/21626.

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

MLA Handbook (7th Edition):

Lewis, Norman G. “Studies on the synthesis and biosynthesis of indole alkaloids .” 1978. Web. 22 May 2019.

Vancouver:

Lewis NG. Studies on the synthesis and biosynthesis of indole alkaloids . [Internet] [Thesis]. University of British Columbia; 1978. [cited 2019 May 22]. Available from: http://hdl.handle.net/2429/21626.

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

Council of Science Editors:

Lewis NG. Studies on the synthesis and biosynthesis of indole alkaloids . [Thesis]. University of British Columbia; 1978. Available from: http://hdl.handle.net/2429/21626

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


University of British Columbia

12. Grierson, David Scott. Studies on the biosynthesis, degradation and synthesis of olivacine-ellipticine type indole alkaloids .

Degree: 1975, University of British Columbia

 Part I of this thesis describes the isolation of representatives of a class of indole alkaloids, lacking the 3-Ƃ-ethylamino side chain, from two plant sources… (more)

Subjects/Keywords: Indole alkaloids

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APA (6th Edition):

Grierson, D. S. (1975). Studies on the biosynthesis, degradation and synthesis of olivacine-ellipticine type indole alkaloids . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/19670

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):

Grierson, David Scott. “Studies on the biosynthesis, degradation and synthesis of olivacine-ellipticine type indole alkaloids .” 1975. Thesis, University of British Columbia. Accessed May 22, 2019. http://hdl.handle.net/2429/19670.

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

MLA Handbook (7th Edition):

Grierson, David Scott. “Studies on the biosynthesis, degradation and synthesis of olivacine-ellipticine type indole alkaloids .” 1975. Web. 22 May 2019.

Vancouver:

Grierson DS. Studies on the biosynthesis, degradation and synthesis of olivacine-ellipticine type indole alkaloids . [Internet] [Thesis]. University of British Columbia; 1975. [cited 2019 May 22]. Available from: http://hdl.handle.net/2429/19670.

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

Council of Science Editors:

Grierson DS. Studies on the biosynthesis, degradation and synthesis of olivacine-ellipticine type indole alkaloids . [Thesis]. University of British Columbia; 1975. Available from: http://hdl.handle.net/2429/19670

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


University of Johannesburg

13. 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 May 22, 2019. 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. 22 May 2019.

Vancouver:

Greyling HF. Die sintese van alkaloiedagtige glikosidase-inhibeerders vanuit monosakkariede. [Internet] [Thesis]. University of Johannesburg; 2014. [cited 2019 May 22]. 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


Universidade do Rio Grande do Sul

14. Fragoso, Variluska. Alcalóides de Psychotria : fotorregulação e propriedades antioxidantes e antimutagênicas.

Degree: 2007, Universidade do Rio Grande do Sul

Espécies de Psychotria encontradas no sul do Brasil produzem alcalóides do tipo monoterpeno indólicos, alguns deles com interessantes atividades biológicas e oriundos de novas rotas… (more)

Subjects/Keywords: Psychotria leiocarpa; Psychotria leiocarpa Cham. & Schlecht; Psychotria umbellata; Psychotria umbellata Vell.; Saccharomyces cerevisiae; Monoterpene indole alkaloids; Atividade antioxidante; N; Biotecnologia vegetal; b-D-Glucopyranosylvincosamide; Psychollatine; Alcalóides; Photoregulation; VLFR; Saccharomyces cerevisiae; Antioxidant activity; Antimutagenic activity

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APA (6th Edition):

Fragoso, V. (2007). Alcalóides de Psychotria : fotorregulação e propriedades antioxidantes e antimutagênicas. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/10958

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):

Fragoso, Variluska. “Alcalóides de Psychotria : fotorregulação e propriedades antioxidantes e antimutagênicas.” 2007. Thesis, Universidade do Rio Grande do Sul. Accessed May 22, 2019. http://hdl.handle.net/10183/10958.

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

MLA Handbook (7th Edition):

Fragoso, Variluska. “Alcalóides de Psychotria : fotorregulação e propriedades antioxidantes e antimutagênicas.” 2007. Web. 22 May 2019.

Vancouver:

Fragoso V. Alcalóides de Psychotria : fotorregulação e propriedades antioxidantes e antimutagênicas. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2007. [cited 2019 May 22]. Available from: http://hdl.handle.net/10183/10958.

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

Council of Science Editors:

Fragoso V. Alcalóides de Psychotria : fotorregulação e propriedades antioxidantes e antimutagênicas. [Thesis]. Universidade do Rio Grande do Sul; 2007. Available from: http://hdl.handle.net/10183/10958

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

15. Chebbi, Mouadh. Implication de facteurs de transcription de type doigt de zinc et de la famille des WRKY dans la régulation de la voie du MEP et de la biosynthèse des alcaloïdes indoliques monoterpéniques de Catharanthus roseus : Involvment of transcription factors of the zinc finger and the WRKY families in the regulation of the MEP pathway and the MIA biosynthesis in Catharanthus roseus.

Degree: Docteur es, Sciences de la vie, spécialité Physiologie végétale, 2015, Université François-Rabelais de Tours

Les alcaloïdes indoliques monoterpéniques (AIM) sont des molécules à propriétés anti-tumorales extraites de Catharanthus roseus. Leur coût de production et les besoins encore importants de… (more)

Subjects/Keywords: Catharanthus roseus; Alcaloïdes indoliques monoterpéniques; Facteurs de transcription; WRKY; ZCT; Méthyl érythritol phosphate; Criblage par simple de levure; Transactivation; Promoteur Crhds; Régulation génique; Catharanthus roseus; Monoterpene indole alkaloids; Transcription factors; WRKY; ZCT; Methyl erythritol phosphate; Yeast one-hybrid screening; Transactivation; Crhds promoter; Gene regulation

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APA (6th Edition):

Chebbi, M. (2015). Implication de facteurs de transcription de type doigt de zinc et de la famille des WRKY dans la régulation de la voie du MEP et de la biosynthèse des alcaloïdes indoliques monoterpéniques de Catharanthus roseus : Involvment of transcription factors of the zinc finger and the WRKY families in the regulation of the MEP pathway and the MIA biosynthesis in Catharanthus roseus. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2015TOUR3801

Chicago Manual of Style (16th Edition):

Chebbi, Mouadh. “Implication de facteurs de transcription de type doigt de zinc et de la famille des WRKY dans la régulation de la voie du MEP et de la biosynthèse des alcaloïdes indoliques monoterpéniques de Catharanthus roseus : Involvment of transcription factors of the zinc finger and the WRKY families in the regulation of the MEP pathway and the MIA biosynthesis in Catharanthus roseus.” 2015. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed May 22, 2019. http://www.theses.fr/2015TOUR3801.

MLA Handbook (7th Edition):

Chebbi, Mouadh. “Implication de facteurs de transcription de type doigt de zinc et de la famille des WRKY dans la régulation de la voie du MEP et de la biosynthèse des alcaloïdes indoliques monoterpéniques de Catharanthus roseus : Involvment of transcription factors of the zinc finger and the WRKY families in the regulation of the MEP pathway and the MIA biosynthesis in Catharanthus roseus.” 2015. Web. 22 May 2019.

Vancouver:

Chebbi M. Implication de facteurs de transcription de type doigt de zinc et de la famille des WRKY dans la régulation de la voie du MEP et de la biosynthèse des alcaloïdes indoliques monoterpéniques de Catharanthus roseus : Involvment of transcription factors of the zinc finger and the WRKY families in the regulation of the MEP pathway and the MIA biosynthesis in Catharanthus roseus. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2015. [cited 2019 May 22]. Available from: http://www.theses.fr/2015TOUR3801.

Council of Science Editors:

Chebbi M. Implication de facteurs de transcription de type doigt de zinc et de la famille des WRKY dans la régulation de la voie du MEP et de la biosynthèse des alcaloïdes indoliques monoterpéniques de Catharanthus roseus : Involvment of transcription factors of the zinc finger and the WRKY families in the regulation of the MEP pathway and the MIA biosynthesis in Catharanthus roseus. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2015. Available from: http://www.theses.fr/2015TOUR3801

16. Putkonen, Tiina. Preparation of Indole Alkaloids via 1,4-Dihydropyridine Stage or Cyano-Masked Iminium Intermediates.

Degree: 2004, Helsinki University of Technology

Methods to synthesise substituted pyridine derivatives utilising 1,4-dihydropyridines were studied. Addition of nucleophiles to N-alkyl pyridinium salts and application of the products to alkaloid synthesis… (more)

Subjects/Keywords: indole alkaloids; 1,4-dihydropyridines; cyano-trapping

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APA (6th Edition):

Putkonen, T. (2004). Preparation of Indole Alkaloids via 1,4-Dihydropyridine Stage or Cyano-Masked Iminium Intermediates. (Thesis). Helsinki University of Technology. Retrieved from http://lib.tkk.fi/Diss/2004/isbn9512268612/

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):

Putkonen, Tiina. “Preparation of Indole Alkaloids via 1,4-Dihydropyridine Stage or Cyano-Masked Iminium Intermediates.” 2004. Thesis, Helsinki University of Technology. Accessed May 22, 2019. http://lib.tkk.fi/Diss/2004/isbn9512268612/.

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

MLA Handbook (7th Edition):

Putkonen, Tiina. “Preparation of Indole Alkaloids via 1,4-Dihydropyridine Stage or Cyano-Masked Iminium Intermediates.” 2004. Web. 22 May 2019.

Vancouver:

Putkonen T. Preparation of Indole Alkaloids via 1,4-Dihydropyridine Stage or Cyano-Masked Iminium Intermediates. [Internet] [Thesis]. Helsinki University of Technology; 2004. [cited 2019 May 22]. Available from: http://lib.tkk.fi/Diss/2004/isbn9512268612/.

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

Council of Science Editors:

Putkonen T. Preparation of Indole Alkaloids via 1,4-Dihydropyridine Stage or Cyano-Masked Iminium Intermediates. [Thesis]. Helsinki University of Technology; 2004. Available from: http://lib.tkk.fi/Diss/2004/isbn9512268612/

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

17. 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 May 22, 2019. 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. 22 May 2019.

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 2019 May 22]. 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.


University of Hong Kong

18. 李輝途; Lee, Victor. Synthetic study of seco-yuehchukene and inverto-yuehchukene.

Degree: M. Phil., 1987, University of Hong Kong

published_or_final_version

Chemistry

Master

Master of Philosophy

Subjects/Keywords: Indole alkaloids - Synthesis.

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APA (6th Edition):

李輝途; Lee, V. (1987). Synthetic study of seco-yuehchukene and inverto-yuehchukene. (Masters Thesis). University of Hong Kong. Retrieved from Lee, V. [李輝途]. (1987). Synthetic study of seco-yuehchukene and inverto-yuehchukene. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3120824 ; http://dx.doi.org/10.5353/th_b3120824 ; http://hdl.handle.net/10722/32314

Chicago Manual of Style (16th Edition):

李輝途; Lee, Victor. “Synthetic study of seco-yuehchukene and inverto-yuehchukene.” 1987. Masters Thesis, University of Hong Kong. Accessed May 22, 2019. Lee, V. [李輝途]. (1987). Synthetic study of seco-yuehchukene and inverto-yuehchukene. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3120824 ; http://dx.doi.org/10.5353/th_b3120824 ; http://hdl.handle.net/10722/32314.

MLA Handbook (7th Edition):

李輝途; Lee, Victor. “Synthetic study of seco-yuehchukene and inverto-yuehchukene.” 1987. Web. 22 May 2019.

Vancouver:

李輝途; Lee V. Synthetic study of seco-yuehchukene and inverto-yuehchukene. [Internet] [Masters thesis]. University of Hong Kong; 1987. [cited 2019 May 22]. Available from: Lee, V. [李輝途]. (1987). Synthetic study of seco-yuehchukene and inverto-yuehchukene. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3120824 ; http://dx.doi.org/10.5353/th_b3120824 ; http://hdl.handle.net/10722/32314.

Council of Science Editors:

李輝途; Lee V. Synthetic study of seco-yuehchukene and inverto-yuehchukene. [Masters Thesis]. University of Hong Kong; 1987. Available from: Lee, V. [李輝途]. (1987). Synthetic study of seco-yuehchukene and inverto-yuehchukene. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3120824 ; http://dx.doi.org/10.5353/th_b3120824 ; http://hdl.handle.net/10722/32314


University of Hong Kong

19. Wong, Tze-tat, Edward. 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: PhD, 1992, University of Hong Kong

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Indole alkaloids - Synthesis.

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APA (6th Edition):

Wong, Tze-tat, E. (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. (Doctoral Dissertation). University of Hong Kong. Retrieved from Wong, T. E. [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, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123285 ; http://dx.doi.org/10.5353/th_b3123285 ; http://hdl.handle.net/10722/34656

Chicago Manual of Style (16th Edition):

Wong, Tze-tat, Edward. “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. Doctoral Dissertation, University of Hong Kong. Accessed May 22, 2019. Wong, T. E. [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, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123285 ; http://dx.doi.org/10.5353/th_b3123285 ; http://hdl.handle.net/10722/34656.

MLA Handbook (7th Edition):

Wong, Tze-tat, Edward. “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. 22 May 2019.

Vancouver:

Wong, Tze-tat E. 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] [Doctoral dissertation]. University of Hong Kong; 1992. [cited 2019 May 22]. Available from: Wong, T. E. [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, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123285 ; http://dx.doi.org/10.5353/th_b3123285 ; http://hdl.handle.net/10722/34656.

Council of Science Editors:

Wong, Tze-tat E. 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. [Doctoral Dissertation]. University of Hong Kong; 1992. Available from: Wong, T. E. [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, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123285 ; http://dx.doi.org/10.5353/th_b3123285 ; http://hdl.handle.net/10722/34656


University of Hong Kong

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

Degree: PhD, 1995, University of Hong Kong

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Subjects/Keywords: Indole alkaloids - Synthesis.

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APA (6th Edition):

張文驥; Cheung, M. (1995). Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. (Doctoral Dissertation). University of Hong Kong. Retrieved from Cheung, M. [張文驥]. (1995). Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123414 ; http://dx.doi.org/10.5353/th_b3123414 ; http://hdl.handle.net/10722/35207

Chicago Manual of Style (16th Edition):

張文驥; Cheung, Man-ki. “Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole.” 1995. Doctoral Dissertation, University of Hong Kong. Accessed May 22, 2019. Cheung, M. [張文驥]. (1995). Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123414 ; http://dx.doi.org/10.5353/th_b3123414 ; http://hdl.handle.net/10722/35207.

MLA Handbook (7th Edition):

張文驥; Cheung, Man-ki. “Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole.” 1995. Web. 22 May 2019.

Vancouver:

張文驥; Cheung M. Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. [Internet] [Doctoral dissertation]. University of Hong Kong; 1995. [cited 2019 May 22]. Available from: Cheung, M. [張文驥]. (1995). Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123414 ; http://dx.doi.org/10.5353/th_b3123414 ; http://hdl.handle.net/10722/35207.

Council of Science Editors:

張文驥; Cheung M. Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. [Doctoral Dissertation]. University of Hong Kong; 1995. Available from: Cheung, M. [張文驥]. (1995). Synthesis of inverto-yuehchukene and substituted 1,2,3,4-tetrahydrocyclopent[b]indole. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3123414 ; http://dx.doi.org/10.5353/th_b3123414 ; http://hdl.handle.net/10722/35207


Oregon State University

21. 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 May 22, 2019. 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. 22 May 2019.

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 2019 May 22]. 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

22. 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 May 22, 2019. 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. 22 May 2019.

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 2019 May 22]. 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 British Columbia

23. Ridaura-Sanz, Vincente Ernesto. Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine .

Degree: 1979, University of British Columbia

 The work presented in this thesis is aimed at the total synthesis of 14,21-dehydrosecodine (1). This substance is an indole derivative with reactive substituents at… (more)

Subjects/Keywords: Indole alkaloids; Biosynthesis

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APA (6th Edition):

Ridaura-Sanz, V. E. (1979). Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/22057

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):

Ridaura-Sanz, Vincente Ernesto. “Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine .” 1979. Thesis, University of British Columbia. Accessed May 22, 2019. http://hdl.handle.net/2429/22057.

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

MLA Handbook (7th Edition):

Ridaura-Sanz, Vincente Ernesto. “Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine .” 1979. Web. 22 May 2019.

Vancouver:

Ridaura-Sanz VE. Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine . [Internet] [Thesis]. University of British Columbia; 1979. [cited 2019 May 22]. Available from: http://hdl.handle.net/2429/22057.

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

Council of Science Editors:

Ridaura-Sanz VE. Novel chromium carbonyl complexes of dihydropyridines and their application to the synthesis of dehydrosecodine . [Thesis]. University of British Columbia; 1979. Available from: http://hdl.handle.net/2429/22057

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


University of Adelaide

24. 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 May 22, 2019. 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. 22 May 2019.

Vancouver:

Liljegren DR. Synthetical experiments related to the indole alkaloids / by David Roland Liljegren. [Internet] [Thesis]. University of Adelaide; 1962. [cited 2019 May 22]. 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 Tasmania

25. Hai, MA. Alkaloids of aristotelia species.

Degree: 1981, University of Tasmania

 A detailed phytochemical examination of the alkaloid content of two species of the family Elaeocarpaceae - Aristotelia serrata W.R.B. Oliver and Aristotelia fruticosa Hook F.… (more)

Subjects/Keywords: Elaeocarpaceae; Alkaloids; Indole alkaloids

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APA (6th Edition):

Hai, M. (1981). Alkaloids of aristotelia species. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/19454/7/whole_HaiMohammadAbdul.pdf

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):

Hai, MA. “Alkaloids of aristotelia species.” 1981. Thesis, University of Tasmania. Accessed May 22, 2019. https://eprints.utas.edu.au/19454/7/whole_HaiMohammadAbdul.pdf.

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

MLA Handbook (7th Edition):

Hai, MA. “Alkaloids of aristotelia species.” 1981. Web. 22 May 2019.

Vancouver:

Hai M. Alkaloids of aristotelia species. [Internet] [Thesis]. University of Tasmania; 1981. [cited 2019 May 22]. Available from: https://eprints.utas.edu.au/19454/7/whole_HaiMohammadAbdul.pdf.

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

Council of Science Editors:

Hai M. Alkaloids of aristotelia species. [Thesis]. University of Tasmania; 1981. Available from: https://eprints.utas.edu.au/19454/7/whole_HaiMohammadAbdul.pdf

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

26. Ginis, Olivia. Identification de facteurs de transcription régulateurs de la voie de biosynthèse des alcaloïdes indoliques monoterpéniques chez Catharanthus roseus : Identification of transcription factors regulating the biosynthesis pathway of monoterpene indole alkaloids in catharanthus roseus.

Degree: Docteur es, Sciences de la vie, spécialité Physiologie végétale, 2012, Université François-Rabelais de Tours

Catharanthus roseus est une plante tropicale qui produit spécifiquement des alcaloïdes indoliques monoterpéniques (AIM) d’intérêt thérapeutique. Chez C. roseus, la branche terpénique incluant la voie… (more)

Subjects/Keywords: Catharanthus roseus; Cultures cellulaires; Alcaloïdes indoliques monoterpéniques; Terpènes; MEP; Promoteur; Facteur de transcription; Phytohormones; Signalisation cytokinine; Biolistique; Criblage par simple hybride de levure; Ingénierie métabolique; Méthylérytritol Phosphate; Catharanthus roseus; Cell cultures; Monoterpene indole alkaloids; Terpanoid; MEP; Promoter; Transcription factor; Plant hormones; Cytokinin signaling; Boilistic; Yeast one-hybrid screening; Metabolic engineering

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APA (6th Edition):

Ginis, O. (2012). Identification de facteurs de transcription régulateurs de la voie de biosynthèse des alcaloïdes indoliques monoterpéniques chez Catharanthus roseus : Identification of transcription factors regulating the biosynthesis pathway of monoterpene indole alkaloids in catharanthus roseus. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2012TOUR4014

Chicago Manual of Style (16th Edition):

Ginis, Olivia. “Identification de facteurs de transcription régulateurs de la voie de biosynthèse des alcaloïdes indoliques monoterpéniques chez Catharanthus roseus : Identification of transcription factors regulating the biosynthesis pathway of monoterpene indole alkaloids in catharanthus roseus.” 2012. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed May 22, 2019. http://www.theses.fr/2012TOUR4014.

MLA Handbook (7th Edition):

Ginis, Olivia. “Identification de facteurs de transcription régulateurs de la voie de biosynthèse des alcaloïdes indoliques monoterpéniques chez Catharanthus roseus : Identification of transcription factors regulating the biosynthesis pathway of monoterpene indole alkaloids in catharanthus roseus.” 2012. Web. 22 May 2019.

Vancouver:

Ginis O. Identification de facteurs de transcription régulateurs de la voie de biosynthèse des alcaloïdes indoliques monoterpéniques chez Catharanthus roseus : Identification of transcription factors regulating the biosynthesis pathway of monoterpene indole alkaloids in catharanthus roseus. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2012. [cited 2019 May 22]. Available from: http://www.theses.fr/2012TOUR4014.

Council of Science Editors:

Ginis O. Identification de facteurs de transcription régulateurs de la voie de biosynthèse des alcaloïdes indoliques monoterpéniques chez Catharanthus roseus : Identification of transcription factors regulating the biosynthesis pathway of monoterpene indole alkaloids in catharanthus roseus. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2012. Available from: http://www.theses.fr/2012TOUR4014


Universidade de Brasília

27. Luciana Machado Ramos. Obtenção do alcalóide indólico bufotenina de sementes de Anadenanthera sp (Fabaceae: Mimosideae) do bioma Cerrado e sua utilização para síntese de substâncias bioativas.

Degree: 2008, Universidade de Brasília

The biome Brazilian Cerrado (Savannah) has a variety of plant species rich in organic chemicals of interest, especially alkaloids, found at different levels in the… (more)

Subjects/Keywords: bufotenine; Anadenanthera; alcalóides indólicos; QUIMICA; indole alkaloids; Anadenanthera; bufotenina

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APA (6th Edition):

Ramos, L. M. (2008). Obtenção do alcalóide indólico bufotenina de sementes de Anadenanthera sp (Fabaceae: Mimosideae) do bioma Cerrado e sua utilização para síntese de substâncias bioativas. (Thesis). Universidade de Brasília. Retrieved from http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=4418

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):

Ramos, Luciana Machado. “Obtenção do alcalóide indólico bufotenina de sementes de Anadenanthera sp (Fabaceae: Mimosideae) do bioma Cerrado e sua utilização para síntese de substâncias bioativas.” 2008. Thesis, Universidade de Brasília. Accessed May 22, 2019. http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=4418.

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

MLA Handbook (7th Edition):

Ramos, Luciana Machado. “Obtenção do alcalóide indólico bufotenina de sementes de Anadenanthera sp (Fabaceae: Mimosideae) do bioma Cerrado e sua utilização para síntese de substâncias bioativas.” 2008. Web. 22 May 2019.

Vancouver:

Ramos LM. Obtenção do alcalóide indólico bufotenina de sementes de Anadenanthera sp (Fabaceae: Mimosideae) do bioma Cerrado e sua utilização para síntese de substâncias bioativas. [Internet] [Thesis]. Universidade de Brasília; 2008. [cited 2019 May 22]. Available from: http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=4418.

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

Council of Science Editors:

Ramos LM. Obtenção do alcalóide indólico bufotenina de sementes de Anadenanthera sp (Fabaceae: Mimosideae) do bioma Cerrado e sua utilização para síntese de substâncias bioativas. [Thesis]. Universidade de Brasília; 2008. Available from: http://bdtd.bce.unb.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=4418

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


University of Hong Kong

28. Au, Tak-yan, Francis. Structures of indole alkaloids from Strychnos angustiflora.

Degree: MS, 1973, University of Hong Kong

(Uncorrected OCR) �Abstract of thesis entitled "Structures of Indole Alkaloids from Strychnos angustiflora" submitted by ~ AU Tak-yan, Francis for the degree of Master of… (more)

Subjects/Keywords: Indole alkaloids; Strychnos angustiflora.

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APA (6th Edition):

Au, Tak-yan, F. (1973). Structures of indole alkaloids from Strychnos angustiflora. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/27404

Chicago Manual of Style (16th Edition):

Au, Tak-yan, Francis. “Structures of indole alkaloids from Strychnos angustiflora.” 1973. Masters Thesis, University of Hong Kong. Accessed May 22, 2019. http://hdl.handle.net/10722/27404.

MLA Handbook (7th Edition):

Au, Tak-yan, Francis. “Structures of indole alkaloids from Strychnos angustiflora.” 1973. Web. 22 May 2019.

Vancouver:

Au, Tak-yan F. Structures of indole alkaloids from Strychnos angustiflora. [Internet] [Masters thesis]. University of Hong Kong; 1973. [cited 2019 May 22]. Available from: http://hdl.handle.net/10722/27404.

Council of Science Editors:

Au, Tak-yan F. Structures of indole alkaloids from Strychnos angustiflora. [Masters Thesis]. University of Hong Kong; 1973. Available from: http://hdl.handle.net/10722/27404


University of St Andrews

29. 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 May 22, 2019. 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. 22 May 2019.

Vancouver:

Johnston CA. Progress towards the synthesis of perophoramidine : formation of the contiguous quaternary centres. [Internet] [Doctoral dissertation]. University of St Andrews; 2013. [cited 2019 May 22]. 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


University of Hong Kong

30. Lam, Shuk-mei. Studies on diazoketone rearrangements and application toward the synthesis of welwistatin.

Degree: PhD, 2013, University of Hong Kong

published_or_final_version

Chemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Chiu, P.

Subjects/Keywords: Indole alkaloids - Synthesis; Diazo compounds

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APA (6th Edition):

Lam, S. (2013). Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. (Doctoral Dissertation). University of Hong Kong. Retrieved from Lam, S. [林淑媚]. (2013). Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153691 ; http://dx.doi.org/10.5353/th_b5153691 ; http://hdl.handle.net/10722/196009

Chicago Manual of Style (16th Edition):

Lam, Shuk-mei. “Studies on diazoketone rearrangements and application toward the synthesis of welwistatin.” 2013. Doctoral Dissertation, University of Hong Kong. Accessed May 22, 2019. Lam, S. [林淑媚]. (2013). Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153691 ; http://dx.doi.org/10.5353/th_b5153691 ; http://hdl.handle.net/10722/196009.

MLA Handbook (7th Edition):

Lam, Shuk-mei. “Studies on diazoketone rearrangements and application toward the synthesis of welwistatin.” 2013. Web. 22 May 2019.

Vancouver:

Lam S. Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. [Internet] [Doctoral dissertation]. University of Hong Kong; 2013. [cited 2019 May 22]. Available from: Lam, S. [林淑媚]. (2013). Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153691 ; http://dx.doi.org/10.5353/th_b5153691 ; http://hdl.handle.net/10722/196009.

Council of Science Editors:

Lam S. Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. [Doctoral Dissertation]. University of Hong Kong; 2013. Available from: Lam, S. [林淑媚]. (2013). Studies on diazoketone rearrangements and application toward the synthesis of welwistatin. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5153691 ; http://dx.doi.org/10.5353/th_b5153691 ; http://hdl.handle.net/10722/196009

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