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You searched for subject:(Natural product). Showing records 1 – 30 of 388 total matches.

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Texas A&M University

1. McFarlin, Rae. Chemoselective Functionalization of Carboxylic Acid and Phenol Containing Natural Products and the Development and Use of a Nucleophile Catalyzed Michael Aldol Lactonization Process.

Degree: 2013, Texas A&M University

 The development of methods for site-selective derivatization of natural products to enable simultaneous arming and structure activity relationship (SAR) studies has shown great potential for… (more)

Subjects/Keywords: natural product functionalization; synthetic methodology

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APA (6th Edition):

McFarlin, R. (2013). Chemoselective Functionalization of Carboxylic Acid and Phenol Containing Natural Products and the Development and Use of a Nucleophile Catalyzed Michael Aldol Lactonization Process. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149474

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):

McFarlin, Rae. “Chemoselective Functionalization of Carboxylic Acid and Phenol Containing Natural Products and the Development and Use of a Nucleophile Catalyzed Michael Aldol Lactonization Process.” 2013. Thesis, Texas A&M University. Accessed December 07, 2019. http://hdl.handle.net/1969.1/149474.

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

MLA Handbook (7th Edition):

McFarlin, Rae. “Chemoselective Functionalization of Carboxylic Acid and Phenol Containing Natural Products and the Development and Use of a Nucleophile Catalyzed Michael Aldol Lactonization Process.” 2013. Web. 07 Dec 2019.

Vancouver:

McFarlin R. Chemoselective Functionalization of Carboxylic Acid and Phenol Containing Natural Products and the Development and Use of a Nucleophile Catalyzed Michael Aldol Lactonization Process. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/1969.1/149474.

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

Council of Science Editors:

McFarlin R. Chemoselective Functionalization of Carboxylic Acid and Phenol Containing Natural Products and the Development and Use of a Nucleophile Catalyzed Michael Aldol Lactonization Process. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/149474

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


Victoria University of Wellington

2. Brown, Sarah. Design and Synthesis of a Highly Simplified Pateamine Analogue.

Degree: 2016, Victoria University of Wellington

 Pateamine (1) is a natural product from the marine sponge Mycale hentscheli that exhibits potent anticancer properties, and has potential as an antiviral agent, and… (more)

Subjects/Keywords: Pateamine; Natural product; Analogue

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APA (6th Edition):

Brown, S. (2016). Design and Synthesis of a Highly Simplified Pateamine Analogue. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/5246

Chicago Manual of Style (16th Edition):

Brown, Sarah. “Design and Synthesis of a Highly Simplified Pateamine Analogue.” 2016. Masters Thesis, Victoria University of Wellington. Accessed December 07, 2019. http://hdl.handle.net/10063/5246.

MLA Handbook (7th Edition):

Brown, Sarah. “Design and Synthesis of a Highly Simplified Pateamine Analogue.” 2016. Web. 07 Dec 2019.

Vancouver:

Brown S. Design and Synthesis of a Highly Simplified Pateamine Analogue. [Internet] [Masters thesis]. Victoria University of Wellington; 2016. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/10063/5246.

Council of Science Editors:

Brown S. Design and Synthesis of a Highly Simplified Pateamine Analogue. [Masters Thesis]. Victoria University of Wellington; 2016. Available from: http://hdl.handle.net/10063/5246


Oregon State University

3. Medina, Rebecca A. Biologically active cyclic depsipeptides from marine cyanobacteria.

Degree: PhD, Pharmacy, 2009, Oregon State University

 This thesis describes the chemical investigation of marine cyanobacteria collected in Madagascar and Panama with an emphasis on the isolation and structure elucidation of medicinally… (more)

Subjects/Keywords: Natural Product Chemistry; Lyngbya

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APA (6th Edition):

Medina, R. A. (2009). Biologically active cyclic depsipeptides from marine cyanobacteria. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/11265

Chicago Manual of Style (16th Edition):

Medina, Rebecca A. “Biologically active cyclic depsipeptides from marine cyanobacteria.” 2009. Doctoral Dissertation, Oregon State University. Accessed December 07, 2019. http://hdl.handle.net/1957/11265.

MLA Handbook (7th Edition):

Medina, Rebecca A. “Biologically active cyclic depsipeptides from marine cyanobacteria.” 2009. Web. 07 Dec 2019.

Vancouver:

Medina RA. Biologically active cyclic depsipeptides from marine cyanobacteria. [Internet] [Doctoral dissertation]. Oregon State University; 2009. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/1957/11265.

Council of Science Editors:

Medina RA. Biologically active cyclic depsipeptides from marine cyanobacteria. [Doctoral Dissertation]. Oregon State University; 2009. Available from: http://hdl.handle.net/1957/11265


University of Southern California

4. Lo, Hsien-Chun. Molecular genetic mining of the secondary metabolome in Aspergillus nidulans.

Degree: PhD, Pharmaceutical Sciences, 2012, University of Southern California

Natural products (secondary metabolites) are an abundant source of bioactive compounds. These small molecules play substantial roles in modern drug development. Aspergillus, a member of… (more)

Subjects/Keywords: Secondary metabolites; Natural product

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APA (6th Edition):

Lo, H. (2012). Molecular genetic mining of the secondary metabolome in Aspergillus nidulans. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/64711/rec/4186

Chicago Manual of Style (16th Edition):

Lo, Hsien-Chun. “Molecular genetic mining of the secondary metabolome in Aspergillus nidulans.” 2012. Doctoral Dissertation, University of Southern California. Accessed December 07, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/64711/rec/4186.

MLA Handbook (7th Edition):

Lo, Hsien-Chun. “Molecular genetic mining of the secondary metabolome in Aspergillus nidulans.” 2012. Web. 07 Dec 2019.

Vancouver:

Lo H. Molecular genetic mining of the secondary metabolome in Aspergillus nidulans. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Dec 07]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/64711/rec/4186.

Council of Science Editors:

Lo H. Molecular genetic mining of the secondary metabolome in Aspergillus nidulans. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/64711/rec/4186


McMaster University

5. Zepeda-Velazquez, Carlos Armando. DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS.

Degree: PhD, 2015, McMaster University

In the thesis, the development of asymmetric organocatalytic [3+3] sequences for the assembly of aminocyclitols is described. A water-based Wittig reaction was developed in order… (more)

Subjects/Keywords: Organocatalysis; (+)-trans-dihydrolycoricidine; Natural product

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APA (6th Edition):

Zepeda-Velazquez, C. A. (2015). DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/18192

Chicago Manual of Style (16th Edition):

Zepeda-Velazquez, Carlos Armando. “DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS.” 2015. Doctoral Dissertation, McMaster University. Accessed December 07, 2019. http://hdl.handle.net/11375/18192.

MLA Handbook (7th Edition):

Zepeda-Velazquez, Carlos Armando. “DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS.” 2015. Web. 07 Dec 2019.

Vancouver:

Zepeda-Velazquez CA. DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS. [Internet] [Doctoral dissertation]. McMaster University; 2015. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/11375/18192.

Council of Science Editors:

Zepeda-Velazquez CA. DEVELOPMENT OF AN ORGANOCATALYTIC [3+3] REACTION SEQUENCE TOWARD AMINOCYCLITOLS AND TOTAL SYNTHESIS OF ANTICANCER AMARYLLIDACEAE ALKALOIDS. [Doctoral Dissertation]. McMaster University; 2015. Available from: http://hdl.handle.net/11375/18192


Virginia Tech

6. Dengada, Amrapali Harishkumar. Isolation and Structural Elucidation of Compounds from Natural Products.

Degree: MS, Chemistry, 2014, Virginia Tech

 Isolation and Structural Elucidation of Compounds from Natural Products Amrapali H. Dengada In continuation of the Kingston group's work to identify new compounds from natural(more)

Subjects/Keywords: Chemistry; Natural Product Chemistry

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APA (6th Edition):

Dengada, A. H. (2014). Isolation and Structural Elucidation of Compounds from Natural Products. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/64303

Chicago Manual of Style (16th Edition):

Dengada, Amrapali Harishkumar. “Isolation and Structural Elucidation of Compounds from Natural Products.” 2014. Masters Thesis, Virginia Tech. Accessed December 07, 2019. http://hdl.handle.net/10919/64303.

MLA Handbook (7th Edition):

Dengada, Amrapali Harishkumar. “Isolation and Structural Elucidation of Compounds from Natural Products.” 2014. Web. 07 Dec 2019.

Vancouver:

Dengada AH. Isolation and Structural Elucidation of Compounds from Natural Products. [Internet] [Masters thesis]. Virginia Tech; 2014. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/10919/64303.

Council of Science Editors:

Dengada AH. Isolation and Structural Elucidation of Compounds from Natural Products. [Masters Thesis]. Virginia Tech; 2014. Available from: http://hdl.handle.net/10919/64303


University of Cambridge

7. Usachova, Katsiaryna. Analysis and Engineering of Polyene Biosynthesis in Actinomycetes .

Degree: 2019, University of Cambridge

 The work in this thesis concerns the biosynthetic pathways to antibiotic natural products in actinomycete bacteria, and evaluates three different approaches to accessing novel chemical… (more)

Subjects/Keywords: Actinomycete; Natural product; Polyene

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APA (6th Edition):

Usachova, K. (2019). Analysis and Engineering of Polyene Biosynthesis in Actinomycetes . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290610

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):

Usachova, Katsiaryna. “Analysis and Engineering of Polyene Biosynthesis in Actinomycetes .” 2019. Thesis, University of Cambridge. Accessed December 07, 2019. https://www.repository.cam.ac.uk/handle/1810/290610.

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

MLA Handbook (7th Edition):

Usachova, Katsiaryna. “Analysis and Engineering of Polyene Biosynthesis in Actinomycetes .” 2019. Web. 07 Dec 2019.

Vancouver:

Usachova K. Analysis and Engineering of Polyene Biosynthesis in Actinomycetes . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Dec 07]. Available from: https://www.repository.cam.ac.uk/handle/1810/290610.

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

Council of Science Editors:

Usachova K. Analysis and Engineering of Polyene Biosynthesis in Actinomycetes . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290610

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


University of Cambridge

8. Gibson, Lisa. Studies towards the total synthesis of the chivosazoles.

Degree: PhD, 2011, University of Cambridge

 The chivosazoles, isolated in 1994 from the myxobacterium Sorangium cellulosum by Höfle and co-workers, are a family of polyketides that exhibit a range of potent… (more)

Subjects/Keywords: 540; Chivosazole; Natural product synthesis

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APA (6th Edition):

Gibson, L. (2011). Studies towards the total synthesis of the chivosazoles. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/241106 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545410

Chicago Manual of Style (16th Edition):

Gibson, Lisa. “Studies towards the total synthesis of the chivosazoles.” 2011. Doctoral Dissertation, University of Cambridge. Accessed December 07, 2019. https://www.repository.cam.ac.uk/handle/1810/241106 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545410.

MLA Handbook (7th Edition):

Gibson, Lisa. “Studies towards the total synthesis of the chivosazoles.” 2011. Web. 07 Dec 2019.

Vancouver:

Gibson L. Studies towards the total synthesis of the chivosazoles. [Internet] [Doctoral dissertation]. University of Cambridge; 2011. [cited 2019 Dec 07]. Available from: https://www.repository.cam.ac.uk/handle/1810/241106 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545410.

Council of Science Editors:

Gibson L. Studies towards the total synthesis of the chivosazoles. [Doctoral Dissertation]. University of Cambridge; 2011. Available from: https://www.repository.cam.ac.uk/handle/1810/241106 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545410


University of Illinois – Urbana-Champaign

9. Yang, Xiao. Biosynthesis and engineering of lanthipeptide natural products for novel applications.

Degree: PhD, Chemistry, 2015, University of Illinois – Urbana-Champaign

Natural products have played prominent roles in science and medicine due to their diverse chemical scaffolds and biological activities. Ribosomally synthesized and post-translationally modified peptides… (more)

Subjects/Keywords: Lanthipeptide; Lantibiotic; natural product; biosynthesis

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APA (6th Edition):

Yang, X. (2015). Biosynthesis and engineering of lanthipeptide natural products for novel applications. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89185

Chicago Manual of Style (16th Edition):

Yang, Xiao. “Biosynthesis and engineering of lanthipeptide natural products for novel applications.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 07, 2019. http://hdl.handle.net/2142/89185.

MLA Handbook (7th Edition):

Yang, Xiao. “Biosynthesis and engineering of lanthipeptide natural products for novel applications.” 2015. Web. 07 Dec 2019.

Vancouver:

Yang X. Biosynthesis and engineering of lanthipeptide natural products for novel applications. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/2142/89185.

Council of Science Editors:

Yang X. Biosynthesis and engineering of lanthipeptide natural products for novel applications. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89185


San Jose State University

10. Liu, Ke. An Investigation of the Natural Products of Some Eremophila Species.

Degree: MS, Chemistry, 2011, San Jose State University

  For centuries, the Australian aboriginals have relied on native plants as a source of medicinal agents. Although they employed a wide range of species… (more)

Subjects/Keywords: Eremophila species; Natural product; Sesquiterpenoid

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APA (6th Edition):

Liu, K. (2011). An Investigation of the Natural Products of Some Eremophila Species. (Masters Thesis). San Jose State University. Retrieved from https://doi.org/10.31979/etd.esw9-bemx ; https://scholarworks.sjsu.edu/etd_theses/4058

Chicago Manual of Style (16th Edition):

Liu, Ke. “An Investigation of the Natural Products of Some Eremophila Species.” 2011. Masters Thesis, San Jose State University. Accessed December 07, 2019. https://doi.org/10.31979/etd.esw9-bemx ; https://scholarworks.sjsu.edu/etd_theses/4058.

MLA Handbook (7th Edition):

Liu, Ke. “An Investigation of the Natural Products of Some Eremophila Species.” 2011. Web. 07 Dec 2019.

Vancouver:

Liu K. An Investigation of the Natural Products of Some Eremophila Species. [Internet] [Masters thesis]. San Jose State University; 2011. [cited 2019 Dec 07]. Available from: https://doi.org/10.31979/etd.esw9-bemx ; https://scholarworks.sjsu.edu/etd_theses/4058.

Council of Science Editors:

Liu K. An Investigation of the Natural Products of Some Eremophila Species. [Masters Thesis]. San Jose State University; 2011. Available from: https://doi.org/10.31979/etd.esw9-bemx ; https://scholarworks.sjsu.edu/etd_theses/4058


Rice University

11. Clinger, Jonathan A. Structure, Function, and Dynamics of Bacterial Phytochromes and Natural Product Biosynthesis Enzymes.

Degree: PhD, Natural Sciences, 2018, Rice University

 X-ray crystallography and solution biophysics experiments were used to study the dynamics of photoreceptor photoconversion and natural product biosynthesis enzyme catalysis. The mechanism of photoconversion… (more)

Subjects/Keywords: Photoconversion dynamics; Natural product enzymes

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APA (6th Edition):

Clinger, J. A. (2018). Structure, Function, and Dynamics of Bacterial Phytochromes and Natural Product Biosynthesis Enzymes. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105755

Chicago Manual of Style (16th Edition):

Clinger, Jonathan A. “Structure, Function, and Dynamics of Bacterial Phytochromes and Natural Product Biosynthesis Enzymes.” 2018. Doctoral Dissertation, Rice University. Accessed December 07, 2019. http://hdl.handle.net/1911/105755.

MLA Handbook (7th Edition):

Clinger, Jonathan A. “Structure, Function, and Dynamics of Bacterial Phytochromes and Natural Product Biosynthesis Enzymes.” 2018. Web. 07 Dec 2019.

Vancouver:

Clinger JA. Structure, Function, and Dynamics of Bacterial Phytochromes and Natural Product Biosynthesis Enzymes. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/1911/105755.

Council of Science Editors:

Clinger JA. Structure, Function, and Dynamics of Bacterial Phytochromes and Natural Product Biosynthesis Enzymes. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105755


University of Alberta

12. Necyk, Candace. The Detection and Causality Assessment of Adverse Events Related to Natural Health Product Use in Community Pharmacies through the Implementation of Active Surveillance.

Degree: MS, Department of Medicine, 2013, University of Alberta

 Background: Natural health products (NHP) are widely used by the public. Since NHPs are pharmacologically active products, their ability to cause adverse reactions (AR) is… (more)

Subjects/Keywords: Natural Health Product; Safety; Active Surveillance

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APA (6th Edition):

Necyk, C. (2013). The Detection and Causality Assessment of Adverse Events Related to Natural Health Product Use in Community Pharmacies through the Implementation of Active Surveillance. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/9306sz64n

Chicago Manual of Style (16th Edition):

Necyk, Candace. “The Detection and Causality Assessment of Adverse Events Related to Natural Health Product Use in Community Pharmacies through the Implementation of Active Surveillance.” 2013. Masters Thesis, University of Alberta. Accessed December 07, 2019. https://era.library.ualberta.ca/files/9306sz64n.

MLA Handbook (7th Edition):

Necyk, Candace. “The Detection and Causality Assessment of Adverse Events Related to Natural Health Product Use in Community Pharmacies through the Implementation of Active Surveillance.” 2013. Web. 07 Dec 2019.

Vancouver:

Necyk C. The Detection and Causality Assessment of Adverse Events Related to Natural Health Product Use in Community Pharmacies through the Implementation of Active Surveillance. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2019 Dec 07]. Available from: https://era.library.ualberta.ca/files/9306sz64n.

Council of Science Editors:

Necyk C. The Detection and Causality Assessment of Adverse Events Related to Natural Health Product Use in Community Pharmacies through the Implementation of Active Surveillance. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/9306sz64n


Texas A&M University

13. Kelly, Gilbert Thomson. Probing the Biosynthesis and Mode of Action of Azinomycin B.

Degree: 2010, Texas A&M University

 Since the isolation of azinomycins A and B in 1954 from the soil bacterium, Streptomyces sahachiroi, these natural products have been synthetic targets. Both compounds… (more)

Subjects/Keywords: Biosynthesis; Bioorganic Chemistry; azinomycin; natural product

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APA (6th Edition):

Kelly, G. T. (2010). Probing the Biosynthesis and Mode of Action of Azinomycin B. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-08-820

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):

Kelly, Gilbert Thomson. “Probing the Biosynthesis and Mode of Action of Azinomycin B.” 2010. Thesis, Texas A&M University. Accessed December 07, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-08-820.

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

MLA Handbook (7th Edition):

Kelly, Gilbert Thomson. “Probing the Biosynthesis and Mode of Action of Azinomycin B.” 2010. Web. 07 Dec 2019.

Vancouver:

Kelly GT. Probing the Biosynthesis and Mode of Action of Azinomycin B. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-08-820.

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

Council of Science Editors:

Kelly GT. Probing the Biosynthesis and Mode of Action of Azinomycin B. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-08-820

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


University of Edinburgh

14. Niblock, Helen Sarah. Synthesis of the C(1)-C(9) fragment of disorazole C1 and novel heterocyclic analogues.

Degree: 2012, University of Edinburgh

 A highly convergent strategy for the synthesis of the antitubulin polyketide disorazole C1 is proposed based around the alkyne precursor I, featuring a novel Evans-Tishchenko/ring… (more)

Subjects/Keywords: 547.59; organic synthesis; disorazole; natural product; oxazole

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APA (6th Edition):

Niblock, H. S. (2012). Synthesis of the C(1)-C(9) fragment of disorazole C1 and novel heterocyclic analogues. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/6251

Chicago Manual of Style (16th Edition):

Niblock, Helen Sarah. “Synthesis of the C(1)-C(9) fragment of disorazole C1 and novel heterocyclic analogues.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed December 07, 2019. http://hdl.handle.net/1842/6251.

MLA Handbook (7th Edition):

Niblock, Helen Sarah. “Synthesis of the C(1)-C(9) fragment of disorazole C1 and novel heterocyclic analogues.” 2012. Web. 07 Dec 2019.

Vancouver:

Niblock HS. Synthesis of the C(1)-C(9) fragment of disorazole C1 and novel heterocyclic analogues. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/1842/6251.

Council of Science Editors:

Niblock HS. Synthesis of the C(1)-C(9) fragment of disorazole C1 and novel heterocyclic analogues. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/6251


NSYSU

15. Hsieh, Chi-hua. Studies on the Natural Products of the Formosan Soft Coral Sinularia sp.

Degree: Master, Marine Resources, 2005, NSYSU

 The chemical constituents of EtOH extracts of the soft coral Sinularia sp. have led to the isolation of nature compoundsï¼1-12ï¼,sinularioperoxides A-Dï¼1-4ï¼, sinulariolins A-Dï¼5-8ï¼, 1a,3b-Dihydroxy-24-methylencholesta-5,9-dieneï¼9ï¼,ï¼3Sï¼-3,7-Dimethyl-nona- 6,8-dienoicacidï¼10ï¼,… (more)

Subjects/Keywords: marine; natural product

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APA (6th Edition):

Hsieh, C. (2005). Studies on the Natural Products of the Formosan Soft Coral Sinularia sp. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816105-233855

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):

Hsieh, Chi-hua. “Studies on the Natural Products of the Formosan Soft Coral Sinularia sp.” 2005. Thesis, NSYSU. Accessed December 07, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816105-233855.

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

MLA Handbook (7th Edition):

Hsieh, Chi-hua. “Studies on the Natural Products of the Formosan Soft Coral Sinularia sp.” 2005. Web. 07 Dec 2019.

Vancouver:

Hsieh C. Studies on the Natural Products of the Formosan Soft Coral Sinularia sp. [Internet] [Thesis]. NSYSU; 2005. [cited 2019 Dec 07]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816105-233855.

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

Council of Science Editors:

Hsieh C. Studies on the Natural Products of the Formosan Soft Coral Sinularia sp. [Thesis]. NSYSU; 2005. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816105-233855

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


NSYSU

16. Teng, Wan-Ting. Lobane Diterpenes and their Biological Activities from Formosan Soft Coral Lobophytum varium.

Degree: Master, Marine Biotechnology and Resources, 2015, NSYSU

 In order to discover bioactive secondary metabolites, we have studied the chemical consitutents from the organic extracts of the soft coral Lobophytum varium, which collected… (more)

Subjects/Keywords: natural product; soft coral; Lobophytum; lobane; bioactivity

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APA (6th Edition):

Teng, W. (2015). Lobane Diterpenes and their Biological Activities from Formosan Soft Coral Lobophytum varium. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0712115-154806

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):

Teng, Wan-Ting. “Lobane Diterpenes and their Biological Activities from Formosan Soft Coral Lobophytum varium.” 2015. Thesis, NSYSU. Accessed December 07, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0712115-154806.

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

MLA Handbook (7th Edition):

Teng, Wan-Ting. “Lobane Diterpenes and their Biological Activities from Formosan Soft Coral Lobophytum varium.” 2015. Web. 07 Dec 2019.

Vancouver:

Teng W. Lobane Diterpenes and their Biological Activities from Formosan Soft Coral Lobophytum varium. [Internet] [Thesis]. NSYSU; 2015. [cited 2019 Dec 07]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0712115-154806.

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

Council of Science Editors:

Teng W. Lobane Diterpenes and their Biological Activities from Formosan Soft Coral Lobophytum varium. [Thesis]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0712115-154806

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


University of Alberta

17. Sullivan, Erin Rae. Enantioselective formation of propargylic alcohols.

Degree: PhD, Department of Chemistry, 2011, University of Alberta

 Propargylic alcohol natural products are found in many species of terrestrial plants and marine organisms. Because these compounds are usually isolated from the natural source… (more)

Subjects/Keywords: Alcohol; Polyyne; Enantioselective; natural product; Propargylic

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

APA (6th Edition):

Sullivan, E. R. (2011). Enantioselective formation of propargylic alcohols. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/mk61rh89v

Chicago Manual of Style (16th Edition):

Sullivan, Erin Rae. “Enantioselective formation of propargylic alcohols.” 2011. Doctoral Dissertation, University of Alberta. Accessed December 07, 2019. https://era.library.ualberta.ca/files/mk61rh89v.

MLA Handbook (7th Edition):

Sullivan, Erin Rae. “Enantioselective formation of propargylic alcohols.” 2011. Web. 07 Dec 2019.

Vancouver:

Sullivan ER. Enantioselective formation of propargylic alcohols. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2019 Dec 07]. Available from: https://era.library.ualberta.ca/files/mk61rh89v.

Council of Science Editors:

Sullivan ER. Enantioselective formation of propargylic alcohols. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/mk61rh89v


UCLA

18. Baker-Tripp, Emma Lee. Total Synthesis of N-Methylwelwitindolinone B Isothiocyanate and Nickel-Catalyzed Reactions of Amide Derivatives.

Degree: Chemistry, 2018, UCLA

 This dissertation describes our efforts toward the total synthesis of N-methyl welwitindolinone B isothioscyanate, as well as the development of reactions involving the nickel-catalyzed activation… (more)

Subjects/Keywords: Chemistry; catalysis; methodology; natural product; nickel; synthesis

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APA (6th Edition):

Baker-Tripp, E. L. (2018). Total Synthesis of N-Methylwelwitindolinone B Isothiocyanate and Nickel-Catalyzed Reactions of Amide Derivatives. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/4pf903kx

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):

Baker-Tripp, Emma Lee. “Total Synthesis of N-Methylwelwitindolinone B Isothiocyanate and Nickel-Catalyzed Reactions of Amide Derivatives.” 2018. Thesis, UCLA. Accessed December 07, 2019. http://www.escholarship.org/uc/item/4pf903kx.

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

MLA Handbook (7th Edition):

Baker-Tripp, Emma Lee. “Total Synthesis of N-Methylwelwitindolinone B Isothiocyanate and Nickel-Catalyzed Reactions of Amide Derivatives.” 2018. Web. 07 Dec 2019.

Vancouver:

Baker-Tripp EL. Total Synthesis of N-Methylwelwitindolinone B Isothiocyanate and Nickel-Catalyzed Reactions of Amide Derivatives. [Internet] [Thesis]. UCLA; 2018. [cited 2019 Dec 07]. Available from: http://www.escholarship.org/uc/item/4pf903kx.

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

Council of Science Editors:

Baker-Tripp EL. Total Synthesis of N-Methylwelwitindolinone B Isothiocyanate and Nickel-Catalyzed Reactions of Amide Derivatives. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/4pf903kx

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


University of Manchester

19. Willis, Mark David. Towards the total synthesis of chaetochalasin A.

Degree: PhD, 2012, University of Manchester

 This thesis describes tin and non-tin mediated approaches towards the total synthesis of chaetochalasin A 1 through an intramolecular domino Diels-Alder approach, and subsequent synthesis… (more)

Subjects/Keywords: 660; Diels-Alder; Natural Product Synthesis

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

APA (6th Edition):

Willis, M. D. (2012). Towards the total synthesis of chaetochalasin A. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/towards-the-total-synthesis-of-chaetochalasin-a(07be20b4-6083-42d3-b0f5-c50088d99e5d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564345

Chicago Manual of Style (16th Edition):

Willis, Mark David. “Towards the total synthesis of chaetochalasin A.” 2012. Doctoral Dissertation, University of Manchester. Accessed December 07, 2019. https://www.research.manchester.ac.uk/portal/en/theses/towards-the-total-synthesis-of-chaetochalasin-a(07be20b4-6083-42d3-b0f5-c50088d99e5d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564345.

MLA Handbook (7th Edition):

Willis, Mark David. “Towards the total synthesis of chaetochalasin A.” 2012. Web. 07 Dec 2019.

Vancouver:

Willis MD. Towards the total synthesis of chaetochalasin A. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2019 Dec 07]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/towards-the-total-synthesis-of-chaetochalasin-a(07be20b4-6083-42d3-b0f5-c50088d99e5d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564345.

Council of Science Editors:

Willis MD. Towards the total synthesis of chaetochalasin A. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/towards-the-total-synthesis-of-chaetochalasin-a(07be20b4-6083-42d3-b0f5-c50088d99e5d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564345


University of California – Berkeley

20. Larson, Kimberly Katherine. The Total Synthesis of Galbulimima Alkaloid (+/-) G. B. 13 and the Development of an Anomalous Heck Reaction.

Degree: Chemistry, 2009, University of California – Berkeley

 This dissertation describes our strategy for the total synthesis of Galbulimima alkaloid (<±>)-G. B. 13. First, an overview of the isolation and structural classification of… (more)

Subjects/Keywords: Organic chemistry; natural product; rhodium hydroarylation

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APA (6th Edition):

Larson, K. K. (2009). The Total Synthesis of Galbulimima Alkaloid (+/-) G. B. 13 and the Development of an Anomalous Heck Reaction. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/3fg3n2n4

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):

Larson, Kimberly Katherine. “The Total Synthesis of Galbulimima Alkaloid (+/-) G. B. 13 and the Development of an Anomalous Heck Reaction.” 2009. Thesis, University of California – Berkeley. Accessed December 07, 2019. http://www.escholarship.org/uc/item/3fg3n2n4.

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

MLA Handbook (7th Edition):

Larson, Kimberly Katherine. “The Total Synthesis of Galbulimima Alkaloid (+/-) G. B. 13 and the Development of an Anomalous Heck Reaction.” 2009. Web. 07 Dec 2019.

Vancouver:

Larson KK. The Total Synthesis of Galbulimima Alkaloid (+/-) G. B. 13 and the Development of an Anomalous Heck Reaction. [Internet] [Thesis]. University of California – Berkeley; 2009. [cited 2019 Dec 07]. Available from: http://www.escholarship.org/uc/item/3fg3n2n4.

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

Council of Science Editors:

Larson KK. The Total Synthesis of Galbulimima Alkaloid (+/-) G. B. 13 and the Development of an Anomalous Heck Reaction. [Thesis]. University of California – Berkeley; 2009. Available from: http://www.escholarship.org/uc/item/3fg3n2n4

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


University of California – Irvine

21. Tartakoff, Samuel Steucek. Progress Towards the Total Synthesis of Steroidal Natural Products Clionastatins A and B.

Degree: Chemistry, 2015, University of California – Irvine

 A total synthesis of naturally occurring polychlorinated steroids, clionastatins A and B, was undertaken. Efforts were first directed at the synthesis of a truncated tricyclic… (more)

Subjects/Keywords: Organic chemistry; Chlorination; Natural Product; Steroid; Synthesis

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APA (6th Edition):

Tartakoff, S. S. (2015). Progress Towards the Total Synthesis of Steroidal Natural Products Clionastatins A and B. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/43q1g6bx

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):

Tartakoff, Samuel Steucek. “Progress Towards the Total Synthesis of Steroidal Natural Products Clionastatins A and B.” 2015. Thesis, University of California – Irvine. Accessed December 07, 2019. http://www.escholarship.org/uc/item/43q1g6bx.

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

MLA Handbook (7th Edition):

Tartakoff, Samuel Steucek. “Progress Towards the Total Synthesis of Steroidal Natural Products Clionastatins A and B.” 2015. Web. 07 Dec 2019.

Vancouver:

Tartakoff SS. Progress Towards the Total Synthesis of Steroidal Natural Products Clionastatins A and B. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2019 Dec 07]. Available from: http://www.escholarship.org/uc/item/43q1g6bx.

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

Council of Science Editors:

Tartakoff SS. Progress Towards the Total Synthesis of Steroidal Natural Products Clionastatins A and B. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/43q1g6bx

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


University of Ottawa

22. McGee, Philippe. Application of Gold(I) Catalysis in the Synthesis of Bridged Carbocycles, (±)-Magellanine and (±)-Salvinorin A .

Degree: 2018, University of Ottawa

 Gold was considered for a long time to be an inert metal and was only in 1986 that the first homogeneous gold-catalyzed transformation was reported.… (more)

Subjects/Keywords: Gold catalysis; Natural product; Total synthesis

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APA (6th Edition):

McGee, P. (2018). Application of Gold(I) Catalysis in the Synthesis of Bridged Carbocycles, (±)-Magellanine and (±)-Salvinorin A . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/38485

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):

McGee, Philippe. “Application of Gold(I) Catalysis in the Synthesis of Bridged Carbocycles, (±)-Magellanine and (±)-Salvinorin A .” 2018. Thesis, University of Ottawa. Accessed December 07, 2019. http://hdl.handle.net/10393/38485.

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

MLA Handbook (7th Edition):

McGee, Philippe. “Application of Gold(I) Catalysis in the Synthesis of Bridged Carbocycles, (±)-Magellanine and (±)-Salvinorin A .” 2018. Web. 07 Dec 2019.

Vancouver:

McGee P. Application of Gold(I) Catalysis in the Synthesis of Bridged Carbocycles, (±)-Magellanine and (±)-Salvinorin A . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/10393/38485.

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

Council of Science Editors:

McGee P. Application of Gold(I) Catalysis in the Synthesis of Bridged Carbocycles, (±)-Magellanine and (±)-Salvinorin A . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/38485

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


Loughborough University

23. Brown, Natalie J. Novel synthetic routes towards the anti-inflammatory mediator resolvin E1, and methodology development.

Degree: PhD, 2015, Loughborough University

 The benefits of fish oil supplementation for inflammation based disorders has been well-documented,[1] prompting investigations into the pathways through which these benefits are achieved. This… (more)

Subjects/Keywords: 615.2; Resolvins; Anti-inflammatory; Indium; Natural product

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APA (6th Edition):

Brown, N. J. (2015). Novel synthetic routes towards the anti-inflammatory mediator resolvin E1, and methodology development. (Doctoral Dissertation). Loughborough University. Retrieved from https://dspace.lboro.ac.uk/2134/19587 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674605

Chicago Manual of Style (16th Edition):

Brown, Natalie J. “Novel synthetic routes towards the anti-inflammatory mediator resolvin E1, and methodology development.” 2015. Doctoral Dissertation, Loughborough University. Accessed December 07, 2019. https://dspace.lboro.ac.uk/2134/19587 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674605.

MLA Handbook (7th Edition):

Brown, Natalie J. “Novel synthetic routes towards the anti-inflammatory mediator resolvin E1, and methodology development.” 2015. Web. 07 Dec 2019.

Vancouver:

Brown NJ. Novel synthetic routes towards the anti-inflammatory mediator resolvin E1, and methodology development. [Internet] [Doctoral dissertation]. Loughborough University; 2015. [cited 2019 Dec 07]. Available from: https://dspace.lboro.ac.uk/2134/19587 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674605.

Council of Science Editors:

Brown NJ. Novel synthetic routes towards the anti-inflammatory mediator resolvin E1, and methodology development. [Doctoral Dissertation]. Loughborough University; 2015. Available from: https://dspace.lboro.ac.uk/2134/19587 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.674605


Temple University

24. Brzozowski, Richard Stephen. Synthesis and Biological Evaluation of Carolacton and Analogs.

Degree: PhD, 2016, Temple University

Chemistry

The oral microbiome represents an extremely diverse environment that harbors many species of bacteria; over 700 different species have been identified overall. These organisms… (more)

Subjects/Keywords: Organic chemistry;

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APA (6th Edition):

Brzozowski, R. S. (2016). Synthesis and Biological Evaluation of Carolacton and Analogs. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,383311

Chicago Manual of Style (16th Edition):

Brzozowski, Richard Stephen. “Synthesis and Biological Evaluation of Carolacton and Analogs.” 2016. Doctoral Dissertation, Temple University. Accessed December 07, 2019. http://digital.library.temple.edu/u?/p245801coll10,383311.

MLA Handbook (7th Edition):

Brzozowski, Richard Stephen. “Synthesis and Biological Evaluation of Carolacton and Analogs.” 2016. Web. 07 Dec 2019.

Vancouver:

Brzozowski RS. Synthesis and Biological Evaluation of Carolacton and Analogs. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2019 Dec 07]. Available from: http://digital.library.temple.edu/u?/p245801coll10,383311.

Council of Science Editors:

Brzozowski RS. Synthesis and Biological Evaluation of Carolacton and Analogs. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,383311


University of Adelaide

25. Pepper, Henry Patrick. Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies.

Degree: 2016, University of Adelaide

 Synthetic efforts towards various meroterpenoid natural products based on biosynthetic speculation were undertaken in order to gain biosynthetic insight and to develop efficient syntheses of… (more)

Subjects/Keywords: chemistry; organic; biomimetic synthesis; natural product synthesis

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APA (6th Edition):

Pepper, H. P. (2016). Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/114063

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):

Pepper, Henry Patrick. “Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies.” 2016. Thesis, University of Adelaide. Accessed December 07, 2019. http://hdl.handle.net/2440/114063.

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

MLA Handbook (7th Edition):

Pepper, Henry Patrick. “Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies.” 2016. Web. 07 Dec 2019.

Vancouver:

Pepper HP. Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies. [Internet] [Thesis]. University of Adelaide; 2016. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/2440/114063.

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

Council of Science Editors:

Pepper HP. Biomimetic synthesis of meroterpenoid natural products using dearomatization strategies. [Thesis]. University of Adelaide; 2016. Available from: http://hdl.handle.net/2440/114063

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


McMaster University

26. Vanner, Stephanie. Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies.

Degree: MSc, 2014, McMaster University

Natural products are an important resource for cancer therapy, with highly potent and diverse anticancer activities. Natural product biosynthesis is well comprehended, however the evolutionary… (more)

Subjects/Keywords: natural product; antibody-drug conjugate; cancer

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APA (6th Edition):

Vanner, S. (2014). Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15390

Chicago Manual of Style (16th Edition):

Vanner, Stephanie. “Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies.” 2014. Masters Thesis, McMaster University. Accessed December 07, 2019. http://hdl.handle.net/11375/15390.

MLA Handbook (7th Edition):

Vanner, Stephanie. “Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies.” 2014. Web. 07 Dec 2019.

Vancouver:

Vanner S. Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/11375/15390.

Council of Science Editors:

Vanner S. Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies. [Masters Thesis]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/15390


University of Cambridge

27. Jin, Jialu. Studies Towards the Total Synthesis of the Chivosazoles .

Degree: 2018, University of Cambridge

 First isolated from the myxobacterium Sorangium cellulosm So Ce12 in 1994, the chivosazoles have been reported to possess antiproliferative activity against human cancer cell lines,… (more)

Subjects/Keywords: Total synthesis; Chivosazoles; Natural product; Anticancer drugs

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APA (6th Edition):

Jin, J. (2018). Studies Towards the Total Synthesis of the Chivosazoles . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/273144

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):

Jin, Jialu. “Studies Towards the Total Synthesis of the Chivosazoles .” 2018. Thesis, University of Cambridge. Accessed December 07, 2019. https://www.repository.cam.ac.uk/handle/1810/273144.

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

MLA Handbook (7th Edition):

Jin, Jialu. “Studies Towards the Total Synthesis of the Chivosazoles .” 2018. Web. 07 Dec 2019.

Vancouver:

Jin J. Studies Towards the Total Synthesis of the Chivosazoles . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Dec 07]. Available from: https://www.repository.cam.ac.uk/handle/1810/273144.

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

Council of Science Editors:

Jin J. Studies Towards the Total Synthesis of the Chivosazoles . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/273144

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


University of Toronto

28. Le, Christine. Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products.

Degree: 2012, University of Toronto

Transition metal-catalyzed olefin hydroacylation represents an atom-economical approach for the synthesis of valuable ketone products. To date, the intermolecular variant of this reaction suffers from… (more)

Subjects/Keywords: Hydroacylation; Octaketide natural product; Rhodium-catalysis; 0490

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APA (6th Edition):

Le, C. (2012). Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33305

Chicago Manual of Style (16th Edition):

Le, Christine. “Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products.” 2012. Masters Thesis, University of Toronto. Accessed December 07, 2019. http://hdl.handle.net/1807/33305.

MLA Handbook (7th Edition):

Le, Christine. “Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products.” 2012. Web. 07 Dec 2019.

Vancouver:

Le C. Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/1807/33305.

Council of Science Editors:

Le C. Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33305


University of Minnesota

29. Niu, Dawen. A Biomimetic Approach to Okilactomycin and Chrolactomycin and The Hexadehydro-Diels-Alder (HDDA) Reaction.

Degree: PhD, Chemistry, 2013, University of Minnesota

 We hypothesized that spirotetronate (+)-okilactomycin (1) and (-)-chrolactomycin (2) are biogenetically derived from a common intermediate, (-)-okilactomycin D (3), which in turn arises via an… (more)

Subjects/Keywords: aryne; benzyne; natural product; spirotetronate; total synthesis

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

APA (6th Edition):

Niu, D. (2013). A Biomimetic Approach to Okilactomycin and Chrolactomycin and The Hexadehydro-Diels-Alder (HDDA) Reaction. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/177120

Chicago Manual of Style (16th Edition):

Niu, Dawen. “A Biomimetic Approach to Okilactomycin and Chrolactomycin and The Hexadehydro-Diels-Alder (HDDA) Reaction.” 2013. Doctoral Dissertation, University of Minnesota. Accessed December 07, 2019. http://hdl.handle.net/11299/177120.

MLA Handbook (7th Edition):

Niu, Dawen. “A Biomimetic Approach to Okilactomycin and Chrolactomycin and The Hexadehydro-Diels-Alder (HDDA) Reaction.” 2013. Web. 07 Dec 2019.

Vancouver:

Niu D. A Biomimetic Approach to Okilactomycin and Chrolactomycin and The Hexadehydro-Diels-Alder (HDDA) Reaction. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/11299/177120.

Council of Science Editors:

Niu D. A Biomimetic Approach to Okilactomycin and Chrolactomycin and The Hexadehydro-Diels-Alder (HDDA) Reaction. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/177120


University of Illinois – Urbana-Champaign

30. Bultman, Michael Scott. Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine.

Degree: PhD, 0335, 2010, University of Illinois – Urbana-Champaign

 Our developments toward the total synthesis of the original and revised structures of palau’amine are presented in this study. This includes the construction of the… (more)

Subjects/Keywords: palau'amine; alkaloid; natural product; synthetic studies

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

APA (6th Edition):

Bultman, M. S. (2010). Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/14694

Chicago Manual of Style (16th Edition):

Bultman, Michael Scott. “Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 07, 2019. http://hdl.handle.net/2142/14694.

MLA Handbook (7th Edition):

Bultman, Michael Scott. “Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine.” 2010. Web. 07 Dec 2019.

Vancouver:

Bultman MS. Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/2142/14694.

Council of Science Editors:

Bultman MS. Efforts Toward the Total Synthesis of the Original and Revised Structures of Palau'amine. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/14694

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