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You searched for subject:(Alkaloid). Showing records 1 – 30 of 150 total matches.

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Cornell University

1. Hinze, Meagan. Marine Natural Product Neurotoxins And The Synthesis Of A Surugatoxin Progenitor .

Degree: 2015, Cornell University

 Marine natural products possess diverse architectures and pharmacology, and have provided scientists with a variety of neurotoxins with the potential to be used as research… (more)

Subjects/Keywords: alkaloid; synthesis; surugatoxin

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APA (6th Edition):

Hinze, M. (2015). Marine Natural Product Neurotoxins And The Synthesis Of A Surugatoxin Progenitor . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/40977

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):

Hinze, Meagan. “Marine Natural Product Neurotoxins And The Synthesis Of A Surugatoxin Progenitor .” 2015. Thesis, Cornell University. Accessed July 02, 2020. http://hdl.handle.net/1813/40977.

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

MLA Handbook (7th Edition):

Hinze, Meagan. “Marine Natural Product Neurotoxins And The Synthesis Of A Surugatoxin Progenitor .” 2015. Web. 02 Jul 2020.

Vancouver:

Hinze M. Marine Natural Product Neurotoxins And The Synthesis Of A Surugatoxin Progenitor . [Internet] [Thesis]. Cornell University; 2015. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1813/40977.

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

Council of Science Editors:

Hinze M. Marine Natural Product Neurotoxins And The Synthesis Of A Surugatoxin Progenitor . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/40977

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


University of Kashmir

2. Zutshi, Usha. Inter relationships in some non tuberous species of Indian Solanum with special reference to the Alkaloid content and the origin of Brinjal;.

Degree: 2014, University of Kashmir

The material for the present study includes 14 species of Solanum including 24 geographical races collected from different parts of India Of the 2000 species… (more)

Subjects/Keywords: Indian-Solanum; Alkaloid; Brinjal

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APA (6th Edition):

Zutshi, U. (2014). Inter relationships in some non tuberous species of Indian Solanum with special reference to the Alkaloid content and the origin of Brinjal;. (Thesis). University of Kashmir. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/24018

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):

Zutshi, Usha. “Inter relationships in some non tuberous species of Indian Solanum with special reference to the Alkaloid content and the origin of Brinjal;.” 2014. Thesis, University of Kashmir. Accessed July 02, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/24018.

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

MLA Handbook (7th Edition):

Zutshi, Usha. “Inter relationships in some non tuberous species of Indian Solanum with special reference to the Alkaloid content and the origin of Brinjal;.” 2014. Web. 02 Jul 2020.

Vancouver:

Zutshi U. Inter relationships in some non tuberous species of Indian Solanum with special reference to the Alkaloid content and the origin of Brinjal;. [Internet] [Thesis]. University of Kashmir; 2014. [cited 2020 Jul 02]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/24018.

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

Council of Science Editors:

Zutshi U. Inter relationships in some non tuberous species of Indian Solanum with special reference to the Alkaloid content and the origin of Brinjal;. [Thesis]. University of Kashmir; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/24018

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


Université Catholique de Louvain

3. Eviolitte, Christophe. Nouvelle application des orthoesters fonctionnalisés : vers la synthèse d'alcaloïdes.

Degree: 2014, Université Catholique de Louvain

Alkaloid Synthesis has always fascinated chemists both by the complexity of the structure of these natural products and by their diversity. To carry out these… (more)

Subjects/Keywords: Synthesis; Alkaloid; Orthoester; Alcaloïde; Synthèse

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APA (6th Edition):

Eviolitte, C. (2014). Nouvelle application des orthoesters fonctionnalisés : vers la synthèse d'alcaloïdes. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/150600

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):

Eviolitte, Christophe. “Nouvelle application des orthoesters fonctionnalisés : vers la synthèse d'alcaloïdes.” 2014. Thesis, Université Catholique de Louvain. Accessed July 02, 2020. http://hdl.handle.net/2078.1/150600.

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

MLA Handbook (7th Edition):

Eviolitte, Christophe. “Nouvelle application des orthoesters fonctionnalisés : vers la synthèse d'alcaloïdes.” 2014. Web. 02 Jul 2020.

Vancouver:

Eviolitte C. Nouvelle application des orthoesters fonctionnalisés : vers la synthèse d'alcaloïdes. [Internet] [Thesis]. Université Catholique de Louvain; 2014. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/2078.1/150600.

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

Council of Science Editors:

Eviolitte C. Nouvelle application des orthoesters fonctionnalisés : vers la synthèse d'alcaloïdes. [Thesis]. Université Catholique de Louvain; 2014. Available from: http://hdl.handle.net/2078.1/150600

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


University of Minnesota

4. Beckman, Karen L. Construction of the hasubanan alkaloid core through an oxidative dearomatization/lewis acid catalyzed cyclization.

Degree: PhD, Chemistry, 2014, University of Minnesota

 Access to novel opioid receptor binding ligands is important as chronic pain continues to be a pervasive problem in healthcare. The hasubanan (HB) alkaloids have… (more)

Subjects/Keywords: Alkaloid; Hasubanan; Hypervalent iodide; Synthesis

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APA (6th Edition):

Beckman, K. L. (2014). Construction of the hasubanan alkaloid core through an oxidative dearomatization/lewis acid catalyzed cyclization. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/165360

Chicago Manual of Style (16th Edition):

Beckman, Karen L. “Construction of the hasubanan alkaloid core through an oxidative dearomatization/lewis acid catalyzed cyclization.” 2014. Doctoral Dissertation, University of Minnesota. Accessed July 02, 2020. http://hdl.handle.net/11299/165360.

MLA Handbook (7th Edition):

Beckman, Karen L. “Construction of the hasubanan alkaloid core through an oxidative dearomatization/lewis acid catalyzed cyclization.” 2014. Web. 02 Jul 2020.

Vancouver:

Beckman KL. Construction of the hasubanan alkaloid core through an oxidative dearomatization/lewis acid catalyzed cyclization. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/11299/165360.

Council of Science Editors:

Beckman KL. Construction of the hasubanan alkaloid core through an oxidative dearomatization/lewis acid catalyzed cyclization. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/165360


University of KwaZulu-Natal

5. [No author]. Progress towards the pyrrolizidine alkaloid xenovenine (223H) via hydroamination.

Degree: 2016, University of KwaZulu-Natal

 Many natural products, pharmaceuticals and fine chemicals possess carbon-nitrogen bonds and thus the formation of such bonds is of great importance. Pyrrolizidine, indolizidine, quinolizidine and… (more)

Subjects/Keywords: Pyrrolizidines.; Alkaloids.; Chemistry.; Pyrrolizidine alkaloid xenovenine.; Hydroamination.

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APA (6th Edition):

author], [. (2016). Progress towards the pyrrolizidine alkaloid xenovenine (223H) via hydroamination. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/13459

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):

author], [No. “Progress towards the pyrrolizidine alkaloid xenovenine (223H) via hydroamination. ” 2016. Thesis, University of KwaZulu-Natal. Accessed July 02, 2020. http://hdl.handle.net/10413/13459.

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

MLA Handbook (7th Edition):

author], [No. “Progress towards the pyrrolizidine alkaloid xenovenine (223H) via hydroamination. ” 2016. Web. 02 Jul 2020.

Vancouver:

author] [. Progress towards the pyrrolizidine alkaloid xenovenine (223H) via hydroamination. [Internet] [Thesis]. University of KwaZulu-Natal; 2016. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/10413/13459.

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

Council of Science Editors:

author] [. Progress towards the pyrrolizidine alkaloid xenovenine (223H) via hydroamination. [Thesis]. University of KwaZulu-Natal; 2016. Available from: http://hdl.handle.net/10413/13459

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


Penn State University

6. Nocket, Anthony Joseph. Total Synthesis of the Tetracyclic Antimalarial Alkaloid (±)-myrioneurinol.

Degree: PhD, Chemistry, 2015, Penn State University

 The first total synthesis of the tetracyclic antimalarial alkaloid myrioneurinol (19) in racemic form has been completed in twenty-seven steps and in 1.8% overall yield… (more)

Subjects/Keywords: Total Synthesis; Alkaloid; Myrioneuron; falciparum; anti-Malarial

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APA (6th Edition):

Nocket, A. J. (2015). Total Synthesis of the Tetracyclic Antimalarial Alkaloid (±)-myrioneurinol. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/26299

Chicago Manual of Style (16th Edition):

Nocket, Anthony Joseph. “Total Synthesis of the Tetracyclic Antimalarial Alkaloid (±)-myrioneurinol.” 2015. Doctoral Dissertation, Penn State University. Accessed July 02, 2020. https://etda.libraries.psu.edu/catalog/26299.

MLA Handbook (7th Edition):

Nocket, Anthony Joseph. “Total Synthesis of the Tetracyclic Antimalarial Alkaloid (±)-myrioneurinol.” 2015. Web. 02 Jul 2020.

Vancouver:

Nocket AJ. Total Synthesis of the Tetracyclic Antimalarial Alkaloid (±)-myrioneurinol. [Internet] [Doctoral dissertation]. Penn State University; 2015. [cited 2020 Jul 02]. Available from: https://etda.libraries.psu.edu/catalog/26299.

Council of Science Editors:

Nocket AJ. Total Synthesis of the Tetracyclic Antimalarial Alkaloid (±)-myrioneurinol. [Doctoral Dissertation]. Penn State University; 2015. Available from: https://etda.libraries.psu.edu/catalog/26299


Penn State University

7. Fodor, Matthew. PART 1. SYNTHESIS STUDIES IN THE PHAKELLIN ALKALOID AREA AND.

Degree: PhD, Chemistry, 2010, Penn State University

 The use of the Pummerer reaction to initiate an oxidative cyclization on substrates bearing an imidazole nucleus provides an efficient means to access members of… (more)

Subjects/Keywords: Pummerer; oxidative cyclization; dibromoagelaspongin; pyrrole-imidazole alkaloid

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APA (6th Edition):

Fodor, M. (2010). PART 1. SYNTHESIS STUDIES IN THE PHAKELLIN ALKALOID AREA AND. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11302

Chicago Manual of Style (16th Edition):

Fodor, Matthew. “PART 1. SYNTHESIS STUDIES IN THE PHAKELLIN ALKALOID AREA AND.” 2010. Doctoral Dissertation, Penn State University. Accessed July 02, 2020. https://etda.libraries.psu.edu/catalog/11302.

MLA Handbook (7th Edition):

Fodor, Matthew. “PART 1. SYNTHESIS STUDIES IN THE PHAKELLIN ALKALOID AREA AND.” 2010. Web. 02 Jul 2020.

Vancouver:

Fodor M. PART 1. SYNTHESIS STUDIES IN THE PHAKELLIN ALKALOID AREA AND. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2020 Jul 02]. Available from: https://etda.libraries.psu.edu/catalog/11302.

Council of Science Editors:

Fodor M. PART 1. SYNTHESIS STUDIES IN THE PHAKELLIN ALKALOID AREA AND. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11302


Penn State University

8. 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 02, 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. 02 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 02]. 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


University of California – Berkeley

9. Kisunzu, Jessica Kristine. A Ring Expansion Strategy Toward the Synthesis of Hetisine-Type C20-Diterpenoid Alkaloids.

Degree: Chemistry, 2014, University of California – Berkeley

 A benzyne insertion ring expansion strategy toward the synthesis of hetisine-type C20-diterpenoid alkaloids has been developed. The first chapter of this manuscript presents an introduction… (more)

Subjects/Keywords: Organic chemistry; Chemistry; benzyne; diterpenoid alkaloid; hetisine

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APA (6th Edition):

Kisunzu, J. K. (2014). A Ring Expansion Strategy Toward the Synthesis of Hetisine-Type C20-Diterpenoid Alkaloids. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/8f4726x5

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):

Kisunzu, Jessica Kristine. “A Ring Expansion Strategy Toward the Synthesis of Hetisine-Type C20-Diterpenoid Alkaloids.” 2014. Thesis, University of California – Berkeley. Accessed July 02, 2020. http://www.escholarship.org/uc/item/8f4726x5.

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

MLA Handbook (7th Edition):

Kisunzu, Jessica Kristine. “A Ring Expansion Strategy Toward the Synthesis of Hetisine-Type C20-Diterpenoid Alkaloids.” 2014. Web. 02 Jul 2020.

Vancouver:

Kisunzu JK. A Ring Expansion Strategy Toward the Synthesis of Hetisine-Type C20-Diterpenoid Alkaloids. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2020 Jul 02]. Available from: http://www.escholarship.org/uc/item/8f4726x5.

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

Council of Science Editors:

Kisunzu JK. A Ring Expansion Strategy Toward the Synthesis of Hetisine-Type C20-Diterpenoid Alkaloids. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/8f4726x5

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


UCLA

10. Smith, Joel Michael. Total Synthesis of Picrinine.

Degree: Chemistry, 2015, UCLA

 Throughout history, organisms have ensured their survival by producing a wide variety of small molecule natural products. These entities commonly serve roles in cell function… (more)

Subjects/Keywords: Organic chemistry; Akuammiline; Alkaloid; Picrinine; Total Synthesis

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APA (6th Edition):

Smith, J. M. (2015). Total Synthesis of Picrinine. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6d93p334

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):

Smith, Joel Michael. “Total Synthesis of Picrinine.” 2015. Thesis, UCLA. Accessed July 02, 2020. http://www.escholarship.org/uc/item/6d93p334.

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

MLA Handbook (7th Edition):

Smith, Joel Michael. “Total Synthesis of Picrinine.” 2015. Web. 02 Jul 2020.

Vancouver:

Smith JM. Total Synthesis of Picrinine. [Internet] [Thesis]. UCLA; 2015. [cited 2020 Jul 02]. Available from: http://www.escholarship.org/uc/item/6d93p334.

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

Council of Science Editors:

Smith JM. Total Synthesis of Picrinine. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/6d93p334

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


University of California – Berkeley

11. House, Sarah Elizabeth. A Unified Approach Toward the Total Synthesis of Lycopodium Alkaloids of the Miscellaneous Class.

Degree: Chemistry, 2010, University of California – Berkeley

 A unified approach to the total synthesis of Lycopodium alkaloids belonging to the miscellaneous class has been developed, wherein a single tetracyclic amine is employed… (more)

Subjects/Keywords: Chemistry; alkaloid; dihydrolycolucine; Lycopodium; nankakurine; spirolucidine; synthesis

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APA (6th Edition):

House, S. E. (2010). A Unified Approach Toward the Total Synthesis of Lycopodium Alkaloids of the Miscellaneous Class. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/48m5m0g7

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):

House, Sarah Elizabeth. “A Unified Approach Toward the Total Synthesis of Lycopodium Alkaloids of the Miscellaneous Class.” 2010. Thesis, University of California – Berkeley. Accessed July 02, 2020. http://www.escholarship.org/uc/item/48m5m0g7.

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

MLA Handbook (7th Edition):

House, Sarah Elizabeth. “A Unified Approach Toward the Total Synthesis of Lycopodium Alkaloids of the Miscellaneous Class.” 2010. Web. 02 Jul 2020.

Vancouver:

House SE. A Unified Approach Toward the Total Synthesis of Lycopodium Alkaloids of the Miscellaneous Class. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2020 Jul 02]. Available from: http://www.escholarship.org/uc/item/48m5m0g7.

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

Council of Science Editors:

House SE. A Unified Approach Toward the Total Synthesis of Lycopodium Alkaloids of the Miscellaneous Class. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/48m5m0g7

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


University of Pennsylvania

12. Gober, Claire Marie. Integration Of Fermentation And Organic Synthesis: Studies Of Roquefortine C And Biosynthetic Derivatives.

Degree: 2017, University of Pennsylvania

 Roquefortine C is one of the most ubiquitous indoline alkaloids of fungal origin. It has been isolated from over 30 different species of Penicillium fungi… (more)

Subjects/Keywords: Fermentation; Indole alkaloid; Roquefortine; Organic Chemistry

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APA (6th Edition):

Gober, C. M. (2017). Integration Of Fermentation And Organic Synthesis: Studies Of Roquefortine C And Biosynthetic Derivatives. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2312

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):

Gober, Claire Marie. “Integration Of Fermentation And Organic Synthesis: Studies Of Roquefortine C And Biosynthetic Derivatives.” 2017. Thesis, University of Pennsylvania. Accessed July 02, 2020. https://repository.upenn.edu/edissertations/2312.

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

MLA Handbook (7th Edition):

Gober, Claire Marie. “Integration Of Fermentation And Organic Synthesis: Studies Of Roquefortine C And Biosynthetic Derivatives.” 2017. Web. 02 Jul 2020.

Vancouver:

Gober CM. Integration Of Fermentation And Organic Synthesis: Studies Of Roquefortine C And Biosynthetic Derivatives. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2020 Jul 02]. Available from: https://repository.upenn.edu/edissertations/2312.

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

Council of Science Editors:

Gober CM. Integration Of Fermentation And Organic Synthesis: Studies Of Roquefortine C And Biosynthetic Derivatives. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2312

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


University of Nairobi

13. Kariuki, Hellen Nyambura. Antinociceptive activities of extracts from selected medicinal plants using animal models .

Degree: 2013, University of Nairobi

 This study reports the findings of the scientific evaluation of selected indigenous plants used by Kenyan communities for the management of pain and painful conditions.… (more)

Subjects/Keywords: Antinociception; Toddalia asiatica; Mice; Alkaloid; dihydrochlerythrine

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APA (6th Edition):

Kariuki, H. N. (2013). Antinociceptive activities of extracts from selected medicinal plants using animal models . (Thesis). University of Nairobi. Retrieved from http://hdl.handle.net/11295/62657

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):

Kariuki, Hellen Nyambura. “Antinociceptive activities of extracts from selected medicinal plants using animal models .” 2013. Thesis, University of Nairobi. Accessed July 02, 2020. http://hdl.handle.net/11295/62657.

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

MLA Handbook (7th Edition):

Kariuki, Hellen Nyambura. “Antinociceptive activities of extracts from selected medicinal plants using animal models .” 2013. Web. 02 Jul 2020.

Vancouver:

Kariuki HN. Antinociceptive activities of extracts from selected medicinal plants using animal models . [Internet] [Thesis]. University of Nairobi; 2013. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/11295/62657.

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

Council of Science Editors:

Kariuki HN. Antinociceptive activities of extracts from selected medicinal plants using animal models . [Thesis]. University of Nairobi; 2013. Available from: http://hdl.handle.net/11295/62657

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


Oregon State University

14. Tonsiengsom, Sorasaree. Studies toward the total synthesis of alkaloids : nagelamide A and D, agelastatin D, dragmacidin A-C, salacin and almazoles.

Degree: PhD, Chemistry, 2007, Oregon State University

 Studies toward the total syntheses of highly potent cytotoxic alkaloids including the bromopyrrole alkaloids and indole alkaloids were conducted and are described. Studies carried out… (more)

Subjects/Keywords: alkaloid; Alkaloids  – Synthesis

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APA (6th Edition):

Tonsiengsom, S. (2007). Studies toward the total synthesis of alkaloids : nagelamide A and D, agelastatin D, dragmacidin A-C, salacin and almazoles. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/3883

Chicago Manual of Style (16th Edition):

Tonsiengsom, Sorasaree. “Studies toward the total synthesis of alkaloids : nagelamide A and D, agelastatin D, dragmacidin A-C, salacin and almazoles.” 2007. Doctoral Dissertation, Oregon State University. Accessed July 02, 2020. http://hdl.handle.net/1957/3883.

MLA Handbook (7th Edition):

Tonsiengsom, Sorasaree. “Studies toward the total synthesis of alkaloids : nagelamide A and D, agelastatin D, dragmacidin A-C, salacin and almazoles.” 2007. Web. 02 Jul 2020.

Vancouver:

Tonsiengsom S. Studies toward the total synthesis of alkaloids : nagelamide A and D, agelastatin D, dragmacidin A-C, salacin and almazoles. [Internet] [Doctoral dissertation]. Oregon State University; 2007. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1957/3883.

Council of Science Editors:

Tonsiengsom S. Studies toward the total synthesis of alkaloids : nagelamide A and D, agelastatin D, dragmacidin A-C, salacin and almazoles. [Doctoral Dissertation]. Oregon State University; 2007. Available from: http://hdl.handle.net/1957/3883


University of Minnesota

15. Seki, Hajime. Cyclic enaminones: methodology development, total synthesis, and library construction.

Degree: PhD, Chemistry, 2011, University of Minnesota

 The cyclic enaminone lies at the core of this entire doctoral work. It possesses exceptionally versatile reactivities, and can thus be utilized in the synthesis… (more)

Subjects/Keywords: Alkaloid; Enaminone; Heterocycle; Indolizidine; Methodology; Quinolizidine; Chemistry

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APA (6th Edition):

Seki, H. (2011). Cyclic enaminones: methodology development, total synthesis, and library construction. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/127080

Chicago Manual of Style (16th Edition):

Seki, Hajime. “Cyclic enaminones: methodology development, total synthesis, and library construction.” 2011. Doctoral Dissertation, University of Minnesota. Accessed July 02, 2020. http://purl.umn.edu/127080.

MLA Handbook (7th Edition):

Seki, Hajime. “Cyclic enaminones: methodology development, total synthesis, and library construction.” 2011. Web. 02 Jul 2020.

Vancouver:

Seki H. Cyclic enaminones: methodology development, total synthesis, and library construction. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2020 Jul 02]. Available from: http://purl.umn.edu/127080.

Council of Science Editors:

Seki H. Cyclic enaminones: methodology development, total synthesis, and library construction. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/127080


Utah State University

16. Zhao, Bo. Alkaloid Production by Hairy Root Cultures.

Degree: PhD, Biological and Irrigation Engineering, 2014, Utah State University

  In the present research, nicotine alkaloid production by Nicotiana tabacum (tobacco) hairy roots and tropane alkaloid production by Hyoscyamus niger hairy roots were investigated.… (more)

Subjects/Keywords: Alkaloid Production; Hairy Root Cultures; Biological Engineering

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APA (6th Edition):

Zhao, B. (2014). Alkaloid Production by Hairy Root Cultures. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/3884

Chicago Manual of Style (16th Edition):

Zhao, Bo. “Alkaloid Production by Hairy Root Cultures.” 2014. Doctoral Dissertation, Utah State University. Accessed July 02, 2020. https://digitalcommons.usu.edu/etd/3884.

MLA Handbook (7th Edition):

Zhao, Bo. “Alkaloid Production by Hairy Root Cultures.” 2014. Web. 02 Jul 2020.

Vancouver:

Zhao B. Alkaloid Production by Hairy Root Cultures. [Internet] [Doctoral dissertation]. Utah State University; 2014. [cited 2020 Jul 02]. Available from: https://digitalcommons.usu.edu/etd/3884.

Council of Science Editors:

Zhao B. Alkaloid Production by Hairy Root Cultures. [Doctoral Dissertation]. Utah State University; 2014. Available from: https://digitalcommons.usu.edu/etd/3884


Colorado State University

17. Newcomb, Eric Thomas. Studies concerning platinum-catalyzed 1,6-enyne cycloisomerizations: a unified synthetic approach to the Gelsemium alkaloids.

Degree: PhD, Chemistry, 2015, Colorado State University

 The development and application of transition metal-catalyzed enyne cyclization reactions is an ever growing and active area of research in modern organic synthesis. One prolific… (more)

Subjects/Keywords: catalysis; gelsemium; total synthesis; cycloisomerization; alkaloid; platinum

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APA (6th Edition):

Newcomb, E. T. (2015). Studies concerning platinum-catalyzed 1,6-enyne cycloisomerizations: a unified synthetic approach to the Gelsemium alkaloids. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/166874

Chicago Manual of Style (16th Edition):

Newcomb, Eric Thomas. “Studies concerning platinum-catalyzed 1,6-enyne cycloisomerizations: a unified synthetic approach to the Gelsemium alkaloids.” 2015. Doctoral Dissertation, Colorado State University. Accessed July 02, 2020. http://hdl.handle.net/10217/166874.

MLA Handbook (7th Edition):

Newcomb, Eric Thomas. “Studies concerning platinum-catalyzed 1,6-enyne cycloisomerizations: a unified synthetic approach to the Gelsemium alkaloids.” 2015. Web. 02 Jul 2020.

Vancouver:

Newcomb ET. Studies concerning platinum-catalyzed 1,6-enyne cycloisomerizations: a unified synthetic approach to the Gelsemium alkaloids. [Internet] [Doctoral dissertation]. Colorado State University; 2015. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/10217/166874.

Council of Science Editors:

Newcomb ET. Studies concerning platinum-catalyzed 1,6-enyne cycloisomerizations: a unified synthetic approach to the Gelsemium alkaloids. [Doctoral Dissertation]. Colorado State University; 2015. Available from: http://hdl.handle.net/10217/166874


University of Bath

18. Williams, Colin Stephen. An enantioselective synthesis of substituted 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocines.

Degree: PhD, 1990, University of Bath

Subjects/Keywords: 547; Alkaloid biosynthesis

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APA (6th Edition):

Williams, C. S. (1990). An enantioselective synthesis of substituted 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocines. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/an-enantioselective-synthesis-of-substituted-123456hexahydro26methano3benzazocines(dc9e2f98-b71c-43bb-998c-5c194186f3a2).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278236

Chicago Manual of Style (16th Edition):

Williams, Colin Stephen. “An enantioselective synthesis of substituted 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocines.” 1990. Doctoral Dissertation, University of Bath. Accessed July 02, 2020. https://researchportal.bath.ac.uk/en/studentthesis/an-enantioselective-synthesis-of-substituted-123456hexahydro26methano3benzazocines(dc9e2f98-b71c-43bb-998c-5c194186f3a2).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278236.

MLA Handbook (7th Edition):

Williams, Colin Stephen. “An enantioselective synthesis of substituted 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocines.” 1990. Web. 02 Jul 2020.

Vancouver:

Williams CS. An enantioselective synthesis of substituted 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocines. [Internet] [Doctoral dissertation]. University of Bath; 1990. [cited 2020 Jul 02]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/an-enantioselective-synthesis-of-substituted-123456hexahydro26methano3benzazocines(dc9e2f98-b71c-43bb-998c-5c194186f3a2).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278236.

Council of Science Editors:

Williams CS. An enantioselective synthesis of substituted 1,2,3,4,5,6-hexahydro-2,6-methano-3-benzazocines. [Doctoral Dissertation]. University of Bath; 1990. Available from: https://researchportal.bath.ac.uk/en/studentthesis/an-enantioselective-synthesis-of-substituted-123456hexahydro26methano3benzazocines(dc9e2f98-b71c-43bb-998c-5c194186f3a2).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278236


Loughborough University

19. James, Stella L. Routes to chiral N-acyliminium ion precursors for the synthesis of optically active pure ring-fused pyrroloisoquinoline alkaloids.

Degree: PhD, 2003, Loughborough University

 Pyrrolisoquinoline (B) is found as a major structural motif of the erythrina alkaloid group of natural products. We recognised that a suitably substituted bicyclic lactam… (more)

Subjects/Keywords: 547; Erythrina alkaloid

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APA (6th Edition):

James, S. L. (2003). Routes to chiral N-acyliminium ion precursors for the synthesis of optically active pure ring-fused pyrroloisoquinoline alkaloids. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/12922

Chicago Manual of Style (16th Edition):

James, Stella L. “Routes to chiral N-acyliminium ion precursors for the synthesis of optically active pure ring-fused pyrroloisoquinoline alkaloids.” 2003. Doctoral Dissertation, Loughborough University. Accessed July 02, 2020. http://hdl.handle.net/2134/12922.

MLA Handbook (7th Edition):

James, Stella L. “Routes to chiral N-acyliminium ion precursors for the synthesis of optically active pure ring-fused pyrroloisoquinoline alkaloids.” 2003. Web. 02 Jul 2020.

Vancouver:

James SL. Routes to chiral N-acyliminium ion precursors for the synthesis of optically active pure ring-fused pyrroloisoquinoline alkaloids. [Internet] [Doctoral dissertation]. Loughborough University; 2003. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/2134/12922.

Council of Science Editors:

James SL. Routes to chiral N-acyliminium ion precursors for the synthesis of optically active pure ring-fused pyrroloisoquinoline alkaloids. [Doctoral Dissertation]. Loughborough University; 2003. Available from: http://hdl.handle.net/2134/12922


Penn State University

20. Sacher, Joshua Ryan. PROGRESS TOWARD A TOTAL SYNTHESIS OF THE MARINE ALKALOID PEROPHORAMIDINE.

Degree: MS, Chemistry, 2009, Penn State University

 ABSTRACT Two strategies toward a synthesis of the marine alkaloid perophoramidine (1) have been investigated. Previous work utilizing a tandem Heck reaction/carbonylation strategy was initially… (more)

Subjects/Keywords: carbonylation; intramolecular; Heck; alkaloid; synthesis; chemistry; organic; marine; perophoramidine

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APA (6th Edition):

Sacher, J. R. (2009). PROGRESS TOWARD A TOTAL SYNTHESIS OF THE MARINE ALKALOID PEROPHORAMIDINE. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/10154

Chicago Manual of Style (16th Edition):

Sacher, Joshua Ryan. “PROGRESS TOWARD A TOTAL SYNTHESIS OF THE MARINE ALKALOID PEROPHORAMIDINE.” 2009. Masters Thesis, Penn State University. Accessed July 02, 2020. https://etda.libraries.psu.edu/catalog/10154.

MLA Handbook (7th Edition):

Sacher, Joshua Ryan. “PROGRESS TOWARD A TOTAL SYNTHESIS OF THE MARINE ALKALOID PEROPHORAMIDINE.” 2009. Web. 02 Jul 2020.

Vancouver:

Sacher JR. PROGRESS TOWARD A TOTAL SYNTHESIS OF THE MARINE ALKALOID PEROPHORAMIDINE. [Internet] [Masters thesis]. Penn State University; 2009. [cited 2020 Jul 02]. Available from: https://etda.libraries.psu.edu/catalog/10154.

Council of Science Editors:

Sacher JR. PROGRESS TOWARD A TOTAL SYNTHESIS OF THE MARINE ALKALOID PEROPHORAMIDINE. [Masters Thesis]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/10154


Penn State University

21. Antoline, Joshua F. Total Synthesis of (±)-meloscine via an Allenyl Azide Cycloaddition/diradical Cyclization Cascade.

Degree: PhD, Chemistry, 2012, Penn State University

 Model studies towards and the total synthesis of the Melodan alkaloid (±)-meloscine (2-1) are described. An allenyl azide cycloaddition/diradical cyclization cascade was employed to form… (more)

Subjects/Keywords: meloscine; diradical; total synthesis; cyclization cascade; alkaloid; allenyl azide

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APA (6th Edition):

Antoline, J. F. (2012). Total Synthesis of (±)-meloscine via an Allenyl Azide Cycloaddition/diradical Cyclization Cascade. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/15365

Chicago Manual of Style (16th Edition):

Antoline, Joshua F. “Total Synthesis of (±)-meloscine via an Allenyl Azide Cycloaddition/diradical Cyclization Cascade.” 2012. Doctoral Dissertation, Penn State University. Accessed July 02, 2020. https://etda.libraries.psu.edu/catalog/15365.

MLA Handbook (7th Edition):

Antoline, Joshua F. “Total Synthesis of (±)-meloscine via an Allenyl Azide Cycloaddition/diradical Cyclization Cascade.” 2012. Web. 02 Jul 2020.

Vancouver:

Antoline JF. Total Synthesis of (±)-meloscine via an Allenyl Azide Cycloaddition/diradical Cyclization Cascade. [Internet] [Doctoral dissertation]. Penn State University; 2012. [cited 2020 Jul 02]. Available from: https://etda.libraries.psu.edu/catalog/15365.

Council of Science Editors:

Antoline JF. Total Synthesis of (±)-meloscine via an Allenyl Azide Cycloaddition/diradical Cyclization Cascade. [Doctoral Dissertation]. Penn State University; 2012. Available from: https://etda.libraries.psu.edu/catalog/15365


Penn State University

22. 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 02, 2020. https://etda.libraries.psu.edu/catalog/27568.

MLA Handbook (7th Edition):

Folda, Tamara Sandra. “Progress Towards the Total Synthesis of (-)-gilbertine.” 2015. Web. 02 Jul 2020.

Vancouver:

Folda TS. Progress Towards the Total Synthesis of (-)-gilbertine. [Internet] [Doctoral dissertation]. Penn State University; 2015. [cited 2020 Jul 02]. 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

23. Heller, Stephen Todd. Heterocycles Old and New: Carbonylazoles as Chemoselective Acylation Reagents and the Synthesis and Applications of Benzindolizinones.

Degree: Chemistry, 2012, University of California – Berkeley

 Carbonylazole derivatives have been shown to be chemoselective and efficient acylating reagents under a variety of conditions. Catalysis with pyridinium salts, as well as with… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Acylation; Benzindolizinone; Erythrina Alkaloid; Heterocycles

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APA (6th Edition):

Heller, S. T. (2012). Heterocycles Old and New: Carbonylazoles as Chemoselective Acylation Reagents and the Synthesis and Applications of Benzindolizinones. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/3k03p8kt

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):

Heller, Stephen Todd. “Heterocycles Old and New: Carbonylazoles as Chemoselective Acylation Reagents and the Synthesis and Applications of Benzindolizinones.” 2012. Thesis, University of California – Berkeley. Accessed July 02, 2020. http://www.escholarship.org/uc/item/3k03p8kt.

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

MLA Handbook (7th Edition):

Heller, Stephen Todd. “Heterocycles Old and New: Carbonylazoles as Chemoselective Acylation Reagents and the Synthesis and Applications of Benzindolizinones.” 2012. Web. 02 Jul 2020.

Vancouver:

Heller ST. Heterocycles Old and New: Carbonylazoles as Chemoselective Acylation Reagents and the Synthesis and Applications of Benzindolizinones. [Internet] [Thesis]. University of California – Berkeley; 2012. [cited 2020 Jul 02]. Available from: http://www.escholarship.org/uc/item/3k03p8kt.

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

Council of Science Editors:

Heller ST. Heterocycles Old and New: Carbonylazoles as Chemoselective Acylation Reagents and the Synthesis and Applications of Benzindolizinones. [Thesis]. University of California – Berkeley; 2012. Available from: http://www.escholarship.org/uc/item/3k03p8kt

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


UCLA

24. Styduhar, Evan Daniel. Enantiospecific Total Synthesis of Welwitindolinone Alkaloids.

Degree: Chemistry, 2015, UCLA

 Chapter one provides a summary of efforts towards the syntheses of the welwitindolinones with bicyclo[4.3.1]decane cores. Emphasis is given to more recent approaches that have… (more)

Subjects/Keywords: Organic chemistry; Alkaloid; Indolyne; Nitrene; Oxabicycle; Total Synthesis; Welwitindolinone

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APA (6th Edition):

Styduhar, E. D. (2015). Enantiospecific Total Synthesis of Welwitindolinone Alkaloids. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/59v1f339

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):

Styduhar, Evan Daniel. “Enantiospecific Total Synthesis of Welwitindolinone Alkaloids.” 2015. Thesis, UCLA. Accessed July 02, 2020. http://www.escholarship.org/uc/item/59v1f339.

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

MLA Handbook (7th Edition):

Styduhar, Evan Daniel. “Enantiospecific Total Synthesis of Welwitindolinone Alkaloids.” 2015. Web. 02 Jul 2020.

Vancouver:

Styduhar ED. Enantiospecific Total Synthesis of Welwitindolinone Alkaloids. [Internet] [Thesis]. UCLA; 2015. [cited 2020 Jul 02]. Available from: http://www.escholarship.org/uc/item/59v1f339.

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

Council of Science Editors:

Styduhar ED. Enantiospecific Total Synthesis of Welwitindolinone Alkaloids. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/59v1f339

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


University of California – Berkeley

25. West, Scott P. Total Synthesis of (±) and (+)-Lyconadin A and Mechanistic Studies of Oxidative C-N Bond Formation.

Degree: Chemistry, 2010, University of California – Berkeley

 An overview of the Lycopodium alkaloids is presented covering their isolation, structural classification and biosynthesis. The isolation, biological activity and biosynthesis of the miscellaneous group… (more)

Subjects/Keywords: Organic chemistry; alkaloid; lyconadin; lycopodium; organic; oxidative; synthesis

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APA (6th Edition):

West, S. P. (2010). Total Synthesis of (±) and (+)-Lyconadin A and Mechanistic Studies of Oxidative C-N Bond Formation. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/5kc8r4pt

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):

West, Scott P. “Total Synthesis of (±) and (+)-Lyconadin A and Mechanistic Studies of Oxidative C-N Bond Formation.” 2010. Thesis, University of California – Berkeley. Accessed July 02, 2020. http://www.escholarship.org/uc/item/5kc8r4pt.

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

MLA Handbook (7th Edition):

West, Scott P. “Total Synthesis of (±) and (+)-Lyconadin A and Mechanistic Studies of Oxidative C-N Bond Formation.” 2010. Web. 02 Jul 2020.

Vancouver:

West SP. Total Synthesis of (±) and (+)-Lyconadin A and Mechanistic Studies of Oxidative C-N Bond Formation. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2020 Jul 02]. Available from: http://www.escholarship.org/uc/item/5kc8r4pt.

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

Council of Science Editors:

West SP. Total Synthesis of (±) and (+)-Lyconadin A and Mechanistic Studies of Oxidative C-N Bond Formation. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/5kc8r4pt

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


University of California – Berkeley

26. Murphy, Rebecca Anne. Toward the Synthesis of the Magellaninone- and Lycopladine-type Lycopodium Alkaloids.

Degree: Chemistry, 2013, University of California – Berkeley

 This dissertation describes our strategy toward the synthesis of a variety of fawcettimine–type Lycopodium alkaloids. The first section focuses on the classification, structure, and historical… (more)

Subjects/Keywords: Chemistry; C-H functionalization; Lycopladine B-D; Lycopodium alkaloid; Magellaninone; Serratine

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APA (6th Edition):

Murphy, R. A. (2013). Toward the Synthesis of the Magellaninone- and Lycopladine-type Lycopodium Alkaloids. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6mq230z7

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):

Murphy, Rebecca Anne. “Toward the Synthesis of the Magellaninone- and Lycopladine-type Lycopodium Alkaloids.” 2013. Thesis, University of California – Berkeley. Accessed July 02, 2020. http://www.escholarship.org/uc/item/6mq230z7.

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

MLA Handbook (7th Edition):

Murphy, Rebecca Anne. “Toward the Synthesis of the Magellaninone- and Lycopladine-type Lycopodium Alkaloids.” 2013. Web. 02 Jul 2020.

Vancouver:

Murphy RA. Toward the Synthesis of the Magellaninone- and Lycopladine-type Lycopodium Alkaloids. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2020 Jul 02]. Available from: http://www.escholarship.org/uc/item/6mq230z7.

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

Council of Science Editors:

Murphy RA. Toward the Synthesis of the Magellaninone- and Lycopladine-type Lycopodium Alkaloids. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/6mq230z7

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


University of California – Berkeley

27. Gallego, Gary Michael. Enantioselective Hydroarylation of Unactivated Ketones with Aryl Pinacolboronic Esters and A Hydrindanone-Based Approach Toward Natural Products.

Degree: Chemistry, 2013, University of California – Berkeley

 The first section of this dissertation describes our efforts to further develop the rhodium–catalyzed 1,2–addition of pinacolboronic ester nucleophiles into unactivated ketones. This reaction represents… (more)

Subjects/Keywords: Chemistry; Boronic Ester; Diterpenoid Alkaloid; Limonoid; Phragmalin; Rhodium

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APA (6th Edition):

Gallego, G. M. (2013). Enantioselective Hydroarylation of Unactivated Ketones with Aryl Pinacolboronic Esters and A Hydrindanone-Based Approach Toward Natural Products. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6n18n878

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):

Gallego, Gary Michael. “Enantioselective Hydroarylation of Unactivated Ketones with Aryl Pinacolboronic Esters and A Hydrindanone-Based Approach Toward Natural Products.” 2013. Thesis, University of California – Berkeley. Accessed July 02, 2020. http://www.escholarship.org/uc/item/6n18n878.

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

MLA Handbook (7th Edition):

Gallego, Gary Michael. “Enantioselective Hydroarylation of Unactivated Ketones with Aryl Pinacolboronic Esters and A Hydrindanone-Based Approach Toward Natural Products.” 2013. Web. 02 Jul 2020.

Vancouver:

Gallego GM. Enantioselective Hydroarylation of Unactivated Ketones with Aryl Pinacolboronic Esters and A Hydrindanone-Based Approach Toward Natural Products. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2020 Jul 02]. Available from: http://www.escholarship.org/uc/item/6n18n878.

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

Council of Science Editors:

Gallego GM. Enantioselective Hydroarylation of Unactivated Ketones with Aryl Pinacolboronic Esters and A Hydrindanone-Based Approach Toward Natural Products. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/6n18n878

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

28. Prado, Viviana da Silva. Estudos visando a síntese do alcaloide indolizidínico (+)-ipalbidina.

Degree: Mestrado, Química Orgânica e Biológica, 2012, University of São Paulo

A ipalbidina é um alcaloide indolizidínico com propriedades analgésica e antirradicais livres. Este alcaloide possui como fonte natural a Ipomoea alba L., uma espécie de… (more)

Subjects/Keywords: alcaloide; alkaloid; chloroketone; clorocetona; enantioselectivity; enantiosseletividade; ipalbidina; ipalbidine

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

APA (6th Edition):

Prado, V. d. S. (2012). Estudos visando a síntese do alcaloide indolizidínico (+)-ipalbidina. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/75/75133/tde-17042012-164758/ ;

Chicago Manual of Style (16th Edition):

Prado, Viviana da Silva. “Estudos visando a síntese do alcaloide indolizidínico (+)-ipalbidina.” 2012. Masters Thesis, University of São Paulo. Accessed July 02, 2020. http://www.teses.usp.br/teses/disponiveis/75/75133/tde-17042012-164758/ ;.

MLA Handbook (7th Edition):

Prado, Viviana da Silva. “Estudos visando a síntese do alcaloide indolizidínico (+)-ipalbidina.” 2012. Web. 02 Jul 2020.

Vancouver:

Prado VdS. Estudos visando a síntese do alcaloide indolizidínico (+)-ipalbidina. [Internet] [Masters thesis]. University of São Paulo; 2012. [cited 2020 Jul 02]. Available from: http://www.teses.usp.br/teses/disponiveis/75/75133/tde-17042012-164758/ ;.

Council of Science Editors:

Prado VdS. Estudos visando a síntese do alcaloide indolizidínico (+)-ipalbidina. [Masters Thesis]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/75/75133/tde-17042012-164758/ ;

29. Wang, Shaohui. Synthetic studies toward palau?ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin.

Degree: 2009, Texas A&M University

 Oroidin alkaloids, also known as pyrrole-imidazole alkaloids, have become a hot area of chemical and biological research due to their diverse and intriguing structural features… (more)

Subjects/Keywords: alkaloid; palau'amine; phakellin; synthesis

…was reported in 1997 by Pettit and co-workers.18 The alkaloid was isolated from Phakellia… …Stylissadines are the dimers of a known oroidin-alkaloid massadine (1.15), which was… 

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

APA (6th Edition):

Wang, S. (2009). Synthetic studies toward palau?ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2680

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):

Wang, Shaohui. “Synthetic studies toward palau?ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin.” 2009. Thesis, Texas A&M University. Accessed July 02, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2680.

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

MLA Handbook (7th Edition):

Wang, Shaohui. “Synthetic studies toward palau?ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin.” 2009. Web. 02 Jul 2020.

Vancouver:

Wang S. Synthetic studies toward palau?ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Jul 02]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2680.

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

Council of Science Editors:

Wang S. Synthetic studies toward palau?ne and enantioselective total synthesis of biogenetically related (+)-phakellin and (+)-monobromophakellin. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2680

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

30. Kumar, Krishan. The use of a combined administration of noscapine, an opium alkaloid and extracts of the roots of withania somnifera in treating skin carcinoma, induced by UV-B radiation, in an animal model; -.

Degree: Biomedical, 2004, Bundelkhand University

None

-

Advisors/Committee Members: Ghosh, N N ;Tiwari, Manisha.

Subjects/Keywords: administration; alkaloid; noscapine; opium; roots

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

APA (6th Edition):

Kumar, K. (2004). The use of a combined administration of noscapine, an opium alkaloid and extracts of the roots of withania somnifera in treating skin carcinoma, induced by UV-B radiation, in an animal model; -. (Thesis). Bundelkhand University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/12369

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):

Kumar, Krishan. “The use of a combined administration of noscapine, an opium alkaloid and extracts of the roots of withania somnifera in treating skin carcinoma, induced by UV-B radiation, in an animal model; -.” 2004. Thesis, Bundelkhand University. Accessed July 02, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/12369.

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

MLA Handbook (7th Edition):

Kumar, Krishan. “The use of a combined administration of noscapine, an opium alkaloid and extracts of the roots of withania somnifera in treating skin carcinoma, induced by UV-B radiation, in an animal model; -.” 2004. Web. 02 Jul 2020.

Vancouver:

Kumar K. The use of a combined administration of noscapine, an opium alkaloid and extracts of the roots of withania somnifera in treating skin carcinoma, induced by UV-B radiation, in an animal model; -. [Internet] [Thesis]. Bundelkhand University; 2004. [cited 2020 Jul 02]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12369.

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

Council of Science Editors:

Kumar K. The use of a combined administration of noscapine, an opium alkaloid and extracts of the roots of withania somnifera in treating skin carcinoma, induced by UV-B radiation, in an animal model; -. [Thesis]. Bundelkhand University; 2004. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12369

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

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