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You searched for subject:(Total Synthesis). Showing records 1 – 30 of 461 total matches.

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1. Kaiser, Thomas Maxwell. The Transannular bis-Michael Reaction in the Synthetic Studies of Celastrol and the Development of Novel Palladium-Catalyzed Reactions.

Degree: 2013, Texas Digital Library

 Pharmaceutical R&D is currently undergoing a productivity crisis. Also, the loss of activity of established medicines continues to reduce the pool of agents capable of… (more)

Subjects/Keywords: Total Synthesis

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APA (6th Edition):

Kaiser, T. M. (2013). The Transannular bis-Michael Reaction in the Synthetic Studies of Celastrol and the Development of Novel Palladium-Catalyzed Reactions. (Thesis). Texas Digital Library. Retrieved from http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66663

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):

Kaiser, Thomas Maxwell. “The Transannular bis-Michael Reaction in the Synthetic Studies of Celastrol and the Development of Novel Palladium-Catalyzed Reactions.” 2013. Thesis, Texas Digital Library. Accessed February 26, 2020. http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66663.

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

MLA Handbook (7th Edition):

Kaiser, Thomas Maxwell. “The Transannular bis-Michael Reaction in the Synthetic Studies of Celastrol and the Development of Novel Palladium-Catalyzed Reactions.” 2013. Web. 26 Feb 2020.

Vancouver:

Kaiser TM. The Transannular bis-Michael Reaction in the Synthetic Studies of Celastrol and the Development of Novel Palladium-Catalyzed Reactions. [Internet] [Thesis]. Texas Digital Library; 2013. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66663.

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

Council of Science Editors:

Kaiser TM. The Transannular bis-Michael Reaction in the Synthetic Studies of Celastrol and the Development of Novel Palladium-Catalyzed Reactions. [Thesis]. Texas Digital Library; 2013. Available from: http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66663

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

2. Huang, Jinhua. Synthetic Studies of Iriomoteolide-1A Total Synthesis of Alotaketal A and an Antifungal O-Hydroxy-P-Quinone Methide Diterpenoid.

Degree: 2013, Texas Digital Library

 Natural products are a rich source of compounds with interesting structures and biological activities. Three bioactive natural products, iriomoteolide-1a, alotaketal A, and an unnamed quinone… (more)

Subjects/Keywords: Total Synthesis

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APA (6th Edition):

Huang, J. (2013). Synthetic Studies of Iriomoteolide-1A Total Synthesis of Alotaketal A and an Antifungal O-Hydroxy-P-Quinone Methide Diterpenoid. (Thesis). Texas Digital Library. Retrieved from http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66691

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):

Huang, Jinhua. “Synthetic Studies of Iriomoteolide-1A Total Synthesis of Alotaketal A and an Antifungal O-Hydroxy-P-Quinone Methide Diterpenoid.” 2013. Thesis, Texas Digital Library. Accessed February 26, 2020. http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66691.

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

MLA Handbook (7th Edition):

Huang, Jinhua. “Synthetic Studies of Iriomoteolide-1A Total Synthesis of Alotaketal A and an Antifungal O-Hydroxy-P-Quinone Methide Diterpenoid.” 2013. Web. 26 Feb 2020.

Vancouver:

Huang J. Synthetic Studies of Iriomoteolide-1A Total Synthesis of Alotaketal A and an Antifungal O-Hydroxy-P-Quinone Methide Diterpenoid. [Internet] [Thesis]. Texas Digital Library; 2013. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66691.

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

Council of Science Editors:

Huang J. Synthetic Studies of Iriomoteolide-1A Total Synthesis of Alotaketal A and an Antifungal O-Hydroxy-P-Quinone Methide Diterpenoid. [Thesis]. Texas Digital Library; 2013. Available from: http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66691

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


University of Oxford

3. Richardson, Melodie. Towards the total synthesis of pectenotoxin-4 : synthesis of the CDE and F rings.

Degree: PhD, 2018, University of Oxford

 <b>Chapter 1: Introduction</b> This chapter outlines the isolation and structural identification of the pectenotoxin (PTX) family of natural products, as well as their reported biological… (more)

Subjects/Keywords: total synthesis

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APA (6th Edition):

Richardson, M. (2018). Towards the total synthesis of pectenotoxin-4 : synthesis of the CDE and F rings. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:29efecd9-60dd-4dc3-8aa0-25a69e03a3bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770676

Chicago Manual of Style (16th Edition):

Richardson, Melodie. “Towards the total synthesis of pectenotoxin-4 : synthesis of the CDE and F rings.” 2018. Doctoral Dissertation, University of Oxford. Accessed February 26, 2020. http://ora.ox.ac.uk/objects/uuid:29efecd9-60dd-4dc3-8aa0-25a69e03a3bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770676.

MLA Handbook (7th Edition):

Richardson, Melodie. “Towards the total synthesis of pectenotoxin-4 : synthesis of the CDE and F rings.” 2018. Web. 26 Feb 2020.

Vancouver:

Richardson M. Towards the total synthesis of pectenotoxin-4 : synthesis of the CDE and F rings. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2020 Feb 26]. Available from: http://ora.ox.ac.uk/objects/uuid:29efecd9-60dd-4dc3-8aa0-25a69e03a3bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770676.

Council of Science Editors:

Richardson M. Towards the total synthesis of pectenotoxin-4 : synthesis of the CDE and F rings. [Doctoral Dissertation]. University of Oxford; 2018. Available from: http://ora.ox.ac.uk/objects/uuid:29efecd9-60dd-4dc3-8aa0-25a69e03a3bd ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770676


Colorado State University

4. Thielman, Jonathan Rhines. Total synthesis of the baulamycins, The.

Degree: PhD, Chemistry, 2020, Colorado State University

 Described herein are the total syntheses of the antibiotic polyketides baulamycin A and baulamycin B. A synthesis giving rise to much of the baulamycins' initially-proposed… (more)

Subjects/Keywords: total synthesis; baulamycin

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APA (6th Edition):

Thielman, J. R. (2020). Total synthesis of the baulamycins, The. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/199800

Chicago Manual of Style (16th Edition):

Thielman, Jonathan Rhines. “Total synthesis of the baulamycins, The.” 2020. Doctoral Dissertation, Colorado State University. Accessed February 26, 2020. http://hdl.handle.net/10217/199800.

MLA Handbook (7th Edition):

Thielman, Jonathan Rhines. “Total synthesis of the baulamycins, The.” 2020. Web. 26 Feb 2020.

Vancouver:

Thielman JR. Total synthesis of the baulamycins, The. [Internet] [Doctoral dissertation]. Colorado State University; 2020. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/10217/199800.

Council of Science Editors:

Thielman JR. Total synthesis of the baulamycins, The. [Doctoral Dissertation]. Colorado State University; 2020. Available from: http://hdl.handle.net/10217/199800


University of Utah

5. Espejo, Vinson Ryan. The total synthesis of Kapakahines E and F: the evolution of the discovery of a unique reaction upon bromopyrroloindolines.

Degree: PhD, Chemistry, 2012, University of Utah

 The C(3)-quaternary substituted pyrroloindoline is a motif that is found in manynatural products; therefore, a suitable methodology that can construct such a motif andhas broad… (more)

Subjects/Keywords: kapakahine; pyrroloindoline; total synthesis

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APA (6th Edition):

Espejo, V. R. (2012). The total synthesis of Kapakahines E and F: the evolution of the discovery of a unique reaction upon bromopyrroloindolines. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/1936/rec/2699

Chicago Manual of Style (16th Edition):

Espejo, Vinson Ryan. “The total synthesis of Kapakahines E and F: the evolution of the discovery of a unique reaction upon bromopyrroloindolines.” 2012. Doctoral Dissertation, University of Utah. Accessed February 26, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/1936/rec/2699.

MLA Handbook (7th Edition):

Espejo, Vinson Ryan. “The total synthesis of Kapakahines E and F: the evolution of the discovery of a unique reaction upon bromopyrroloindolines.” 2012. Web. 26 Feb 2020.

Vancouver:

Espejo VR. The total synthesis of Kapakahines E and F: the evolution of the discovery of a unique reaction upon bromopyrroloindolines. [Internet] [Doctoral dissertation]. University of Utah; 2012. [cited 2020 Feb 26]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/1936/rec/2699.

Council of Science Editors:

Espejo VR. The total synthesis of Kapakahines E and F: the evolution of the discovery of a unique reaction upon bromopyrroloindolines. [Doctoral Dissertation]. University of Utah; 2012. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/1936/rec/2699


University of Rochester

6. Srinivasan, Venkatesan. Studies directed toward the total synthesis of (-)-apoptolidin A.

Degree: PhD, 2009, University of Rochester

 Progress towards the total synthesis of the cell specific apoptosis inducer (-)-Apoptolidin A is described. Part of this study includes development of a robust procedure… (more)

Subjects/Keywords: Total synthesis; Apoptolidin A; Apoptosis

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APA (6th Edition):

Srinivasan, V. (2009). Studies directed toward the total synthesis of (-)-apoptolidin A. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/7145

Chicago Manual of Style (16th Edition):

Srinivasan, Venkatesan. “Studies directed toward the total synthesis of (-)-apoptolidin A.” 2009. Doctoral Dissertation, University of Rochester. Accessed February 26, 2020. http://hdl.handle.net/1802/7145.

MLA Handbook (7th Edition):

Srinivasan, Venkatesan. “Studies directed toward the total synthesis of (-)-apoptolidin A.” 2009. Web. 26 Feb 2020.

Vancouver:

Srinivasan V. Studies directed toward the total synthesis of (-)-apoptolidin A. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/1802/7145.

Council of Science Editors:

Srinivasan V. Studies directed toward the total synthesis of (-)-apoptolidin A. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/7145


University of Rochester

7. Tusch, Douglas J. (1988 - ). Part I. Studies Towards the Total Synthesis of (-)-Apoptolidin A Part II. Hydroxymethylation of Aldehydes and Its Application to (-)-Rasfonin.

Degree: PhD, 2017, University of Rochester

 Part I. Studies Towards the Total Synthesis of (-)-Apoptolidin A An approach to the total synthesis of the potent anti-tumor agent (-)-Apoptolidin A has been… (more)

Subjects/Keywords: Apoptolidin; Rasfonin; Hydroxymethylation; Total synthesis

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APA (6th Edition):

Tusch, D. J. (. -. ). (2017). Part I. Studies Towards the Total Synthesis of (-)-Apoptolidin A Part II. Hydroxymethylation of Aldehydes and Its Application to (-)-Rasfonin. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/32994

Chicago Manual of Style (16th Edition):

Tusch, Douglas J (1988 - ). “Part I. Studies Towards the Total Synthesis of (-)-Apoptolidin A Part II. Hydroxymethylation of Aldehydes and Its Application to (-)-Rasfonin.” 2017. Doctoral Dissertation, University of Rochester. Accessed February 26, 2020. http://hdl.handle.net/1802/32994.

MLA Handbook (7th Edition):

Tusch, Douglas J (1988 - ). “Part I. Studies Towards the Total Synthesis of (-)-Apoptolidin A Part II. Hydroxymethylation of Aldehydes and Its Application to (-)-Rasfonin.” 2017. Web. 26 Feb 2020.

Vancouver:

Tusch DJ(-). Part I. Studies Towards the Total Synthesis of (-)-Apoptolidin A Part II. Hydroxymethylation of Aldehydes and Its Application to (-)-Rasfonin. [Internet] [Doctoral dissertation]. University of Rochester; 2017. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/1802/32994.

Council of Science Editors:

Tusch DJ(-). Part I. Studies Towards the Total Synthesis of (-)-Apoptolidin A Part II. Hydroxymethylation of Aldehydes and Its Application to (-)-Rasfonin. [Doctoral Dissertation]. University of Rochester; 2017. Available from: http://hdl.handle.net/1802/32994


University of Notre Dame

8. Vince Lombardo. The Total Synthesis of 20-Deoxyapoptolidinone</h1>.

Degree: PhD, Chemistry and Biochemistry, 2012, University of Notre Dame

  The polyketide apoptolidin is an example from a class a class of 20-membered macrolides with potent and selective apoptosis-inducing activity and are believed to… (more)

Subjects/Keywords: Total Synthesis; 20-Deoxyapoptolidinone

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APA (6th Edition):

Lombardo, V. (2012). The Total Synthesis of 20-Deoxyapoptolidinone</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/vt150g37m7v

Chicago Manual of Style (16th Edition):

Lombardo, Vince. “The Total Synthesis of 20-Deoxyapoptolidinone</h1>.” 2012. Doctoral Dissertation, University of Notre Dame. Accessed February 26, 2020. https://curate.nd.edu/show/vt150g37m7v.

MLA Handbook (7th Edition):

Lombardo, Vince. “The Total Synthesis of 20-Deoxyapoptolidinone</h1>.” 2012. Web. 26 Feb 2020.

Vancouver:

Lombardo V. The Total Synthesis of 20-Deoxyapoptolidinone</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2020 Feb 26]. Available from: https://curate.nd.edu/show/vt150g37m7v.

Council of Science Editors:

Lombardo V. The Total Synthesis of 20-Deoxyapoptolidinone</h1>. [Doctoral Dissertation]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/vt150g37m7v


University of Notre Dame

9. Kai Liu. Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>.

Degree: PhD, Chemistry and Biochemistry, 2009, University of Notre Dame

  Numerous polyketide natural products contain methyl ether functionality generated by either methoxymalonyl extender units or a selective O-methyl transferase associated with the polyketide synthase… (more)

Subjects/Keywords: ether transfer total synthesis

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APA (6th Edition):

Liu, K. (2009). Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/7h149p30z94

Chicago Manual of Style (16th Edition):

Liu, Kai. “Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>.” 2009. Doctoral Dissertation, University of Notre Dame. Accessed February 26, 2020. https://curate.nd.edu/show/7h149p30z94.

MLA Handbook (7th Edition):

Liu, Kai. “Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>.” 2009. Web. 26 Feb 2020.

Vancouver:

Liu K. Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2009. [cited 2020 Feb 26]. Available from: https://curate.nd.edu/show/7h149p30z94.

Council of Science Editors:

Liu K. Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>. [Doctoral Dissertation]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/7h149p30z94


University of Southern California

10. Zhu, Min. Total synthesis of specialized pro-resolving lipid mediators and their analogs.

Degree: PhD, Chemistry, 2013, University of Southern California

 This dissertation reports research on the total synthesis of a series of DHA-derived specialized pro-resolving mediators (SPMs), which can be divided into four projects corresponding… (more)

Subjects/Keywords: total synthesis; lipid mediator

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APA (6th Edition):

Zhu, M. (2013). Total synthesis of specialized pro-resolving lipid mediators and their analogs. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/353055/rec/7508

Chicago Manual of Style (16th Edition):

Zhu, Min. “Total synthesis of specialized pro-resolving lipid mediators and their analogs.” 2013. Doctoral Dissertation, University of Southern California. Accessed February 26, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/353055/rec/7508.

MLA Handbook (7th Edition):

Zhu, Min. “Total synthesis of specialized pro-resolving lipid mediators and their analogs.” 2013. Web. 26 Feb 2020.

Vancouver:

Zhu M. Total synthesis of specialized pro-resolving lipid mediators and their analogs. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Feb 26]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/353055/rec/7508.

Council of Science Editors:

Zhu M. Total synthesis of specialized pro-resolving lipid mediators and their analogs. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/353055/rec/7508


University of Illinois – Urbana-Champaign

11. Holycross, Daniel Robert. Total synthesis of lycoricidine via photochemical dearomative dihydroxylation.

Degree: MS, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Lycoricidine a member of the amaryllidaceae isocarbostyril alkaloid family of natural products isolated from bulbs of plants in the amaryllidaceae family, which include the common… (more)

Subjects/Keywords: Lycoricidine; total synthesis; dearomative dihydroxylation

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APA (6th Edition):

Holycross, D. R. (2016). Total synthesis of lycoricidine via photochemical dearomative dihydroxylation. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95520

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):

Holycross, Daniel Robert. “Total synthesis of lycoricidine via photochemical dearomative dihydroxylation.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed February 26, 2020. http://hdl.handle.net/2142/95520.

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

MLA Handbook (7th Edition):

Holycross, Daniel Robert. “Total synthesis of lycoricidine via photochemical dearomative dihydroxylation.” 2016. Web. 26 Feb 2020.

Vancouver:

Holycross DR. Total synthesis of lycoricidine via photochemical dearomative dihydroxylation. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/2142/95520.

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

Council of Science Editors:

Holycross DR. Total synthesis of lycoricidine via photochemical dearomative dihydroxylation. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95520

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


University of St. Andrews

12. McLennan, Ross Sinclair. Studies towards the total synthesis of the pyrronazols .

Degree: 2019, University of St. Andrews

 In 2014, the pyrronazols, a family of closely related natural products were isolated from a soil dwelling myxobacteria, Nannocystis pusilla strain Ari7. The family represent… (more)

Subjects/Keywords: Natural products; Total synthesis

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APA (6th Edition):

McLennan, R. S. (2019). Studies towards the total synthesis of the pyrronazols . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/17368

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):

McLennan, Ross Sinclair. “Studies towards the total synthesis of the pyrronazols .” 2019. Thesis, University of St. Andrews. Accessed February 26, 2020. http://hdl.handle.net/10023/17368.

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

MLA Handbook (7th Edition):

McLennan, Ross Sinclair. “Studies towards the total synthesis of the pyrronazols .” 2019. Web. 26 Feb 2020.

Vancouver:

McLennan RS. Studies towards the total synthesis of the pyrronazols . [Internet] [Thesis]. University of St. Andrews; 2019. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/10023/17368.

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

Council of Science Editors:

McLennan RS. Studies towards the total synthesis of the pyrronazols . [Thesis]. University of St. Andrews; 2019. Available from: http://hdl.handle.net/10023/17368

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


Cornell University

13. Moschitto, Matthew. Synthesis And Manipulation Of Carbasugars And Natural Product Scaffolds .

Degree: 2016, Cornell University

 My doctoral studies have focused on the construction of natural products and diversification of complex natural product scaffolds. A specific natural product with interesting bioactivity,… (more)

Subjects/Keywords: Organic Chemistry; Total Synthesis; Catalysis

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APA (6th Edition):

Moschitto, M. (2016). Synthesis And Manipulation Of Carbasugars And Natural Product Scaffolds . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/44346

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):

Moschitto, Matthew. “Synthesis And Manipulation Of Carbasugars And Natural Product Scaffolds .” 2016. Thesis, Cornell University. Accessed February 26, 2020. http://hdl.handle.net/1813/44346.

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

MLA Handbook (7th Edition):

Moschitto, Matthew. “Synthesis And Manipulation Of Carbasugars And Natural Product Scaffolds .” 2016. Web. 26 Feb 2020.

Vancouver:

Moschitto M. Synthesis And Manipulation Of Carbasugars And Natural Product Scaffolds . [Internet] [Thesis]. Cornell University; 2016. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/1813/44346.

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

Council of Science Editors:

Moschitto M. Synthesis And Manipulation Of Carbasugars And Natural Product Scaffolds . [Thesis]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/44346

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


Australian National University

14. Drew, Samuel. Explorations in polyene chemistry .

Degree: 2015, Australian National University

 Conjugated polyenes are an important class of organic molecules that have found applications in chemistry, medicine, and materials science. The ability of π-bond rich polyenes… (more)

Subjects/Keywords: total synthesis; natural products; polyenes

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APA (6th Edition):

Drew, S. (2015). Explorations in polyene chemistry . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/98324

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):

Drew, Samuel. “Explorations in polyene chemistry .” 2015. Thesis, Australian National University. Accessed February 26, 2020. http://hdl.handle.net/1885/98324.

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

MLA Handbook (7th Edition):

Drew, Samuel. “Explorations in polyene chemistry .” 2015. Web. 26 Feb 2020.

Vancouver:

Drew S. Explorations in polyene chemistry . [Internet] [Thesis]. Australian National University; 2015. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/1885/98324.

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

Council of Science Editors:

Drew S. Explorations in polyene chemistry . [Thesis]. Australian National University; 2015. Available from: http://hdl.handle.net/1885/98324

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

15. Chen, Joanna. Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins.

Degree: 2017, University of California – eScholarship, University of California

 Cyanobacteria, also known as blue-green algae, are prokaryotic organisms that inhabit freshwater and brackish lakes. They produce toxic secondary metabolites known as cyanotoxins, the increased… (more)

Subjects/Keywords: Organic chemistry; natural product synthesis; total synthesis

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APA (6th Edition):

Chen, J. (2017). Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins. (Thesis). University of California – eScholarship, University of California. Retrieved from http://www.escholarship.org/uc/item/5m39680q

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):

Chen, Joanna. “Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins.” 2017. Thesis, University of California – eScholarship, University of California. Accessed February 26, 2020. http://www.escholarship.org/uc/item/5m39680q.

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

MLA Handbook (7th Edition):

Chen, Joanna. “Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins.” 2017. Web. 26 Feb 2020.

Vancouver:

Chen J. Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins. [Internet] [Thesis]. University of California – eScholarship, University of California; 2017. [cited 2020 Feb 26]. Available from: http://www.escholarship.org/uc/item/5m39680q.

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

Council of Science Editors:

Chen J. Total Synthesis of Isotopically-Labeled Cylindrospermopsin Cyanotoxins. [Thesis]. University of California – eScholarship, University of California; 2017. Available from: http://www.escholarship.org/uc/item/5m39680q

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

16. Herrmann, Aaron Thomas. Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations.

Degree: 2015, University of California – eScholarship, University of California

 Marine natural products have long served as promising compounds and scaffolds for new therapeutic agents; however, their utilization is often extremely limited due to poor… (more)

Subjects/Keywords: Chemistry; Chemistry; Methodology; Organic; Synthesis; Total Synthesis

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APA (6th Edition):

Herrmann, A. T. (2015). Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations. (Thesis). University of California – eScholarship, University of California. Retrieved from http://www.escholarship.org/uc/item/8fd8138z

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):

Herrmann, Aaron Thomas. “Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations.” 2015. Thesis, University of California – eScholarship, University of California. Accessed February 26, 2020. http://www.escholarship.org/uc/item/8fd8138z.

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

MLA Handbook (7th Edition):

Herrmann, Aaron Thomas. “Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations.” 2015. Web. 26 Feb 2020.

Vancouver:

Herrmann AT. Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations. [Internet] [Thesis]. University of California – eScholarship, University of California; 2015. [cited 2020 Feb 26]. Available from: http://www.escholarship.org/uc/item/8fd8138z.

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

Council of Science Editors:

Herrmann AT. Total Synthesis of Bioactive Marine Natural Products Inspired by Enolate Chemsitry & Developments of New Haloalkylations via Soft Enolizations. [Thesis]. University of California – eScholarship, University of California; 2015. Available from: http://www.escholarship.org/uc/item/8fd8138z

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


University of New South Wales

17. Wangsahardja, Jonatan. Towards a treatment for stroke: a novel synthesis of dictyoquinazol A.

Degree: Chemistry, 2015, University of New South Wales

 Stroke can be defined as a loss of brain function due to a disturbance of the blood flow. There are two types of stroke: ischemic… (more)

Subjects/Keywords: Synthesis; Stroke; Total synthesis; Dictyoquinazol; Dictyoquinazols; Analogue

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APA (6th Edition):

Wangsahardja, J. (2015). Towards a treatment for stroke: a novel synthesis of dictyoquinazol A. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55297 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37056/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Wangsahardja, Jonatan. “Towards a treatment for stroke: a novel synthesis of dictyoquinazol A.” 2015. Masters Thesis, University of New South Wales. Accessed February 26, 2020. http://handle.unsw.edu.au/1959.4/55297 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37056/SOURCE02?view=true.

MLA Handbook (7th Edition):

Wangsahardja, Jonatan. “Towards a treatment for stroke: a novel synthesis of dictyoquinazol A.” 2015. Web. 26 Feb 2020.

Vancouver:

Wangsahardja J. Towards a treatment for stroke: a novel synthesis of dictyoquinazol A. [Internet] [Masters thesis]. University of New South Wales; 2015. [cited 2020 Feb 26]. Available from: http://handle.unsw.edu.au/1959.4/55297 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37056/SOURCE02?view=true.

Council of Science Editors:

Wangsahardja J. Towards a treatment for stroke: a novel synthesis of dictyoquinazol A. [Masters Thesis]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55297 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:37056/SOURCE02?view=true


University of Cambridge

18. Reich, Dominik. A novel photocatalytic strategy for complex aliphatic amine synthesis and the total synthesis of alkaloids (−) FR901483 and (+)-TAN1251C.

Degree: PhD, 2020, University of Cambridge

 Owing to their unique properties, the synthesis and functionalization of aliphatic amines plays a central role in the field of visible light photoredox chemistry. In… (more)

Subjects/Keywords: total synthesis; amine synthesis; photoredox catalysis

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APA (6th Edition):

Reich, D. (2020). A novel photocatalytic strategy for complex aliphatic amine synthesis and the total synthesis of alkaloids (−) FR901483 and (+)-TAN1251C. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/301779

Chicago Manual of Style (16th Edition):

Reich, Dominik. “A novel photocatalytic strategy for complex aliphatic amine synthesis and the total synthesis of alkaloids (−) FR901483 and (+)-TAN1251C.” 2020. Doctoral Dissertation, University of Cambridge. Accessed February 26, 2020. https://www.repository.cam.ac.uk/handle/1810/301779.

MLA Handbook (7th Edition):

Reich, Dominik. “A novel photocatalytic strategy for complex aliphatic amine synthesis and the total synthesis of alkaloids (−) FR901483 and (+)-TAN1251C.” 2020. Web. 26 Feb 2020.

Vancouver:

Reich D. A novel photocatalytic strategy for complex aliphatic amine synthesis and the total synthesis of alkaloids (−) FR901483 and (+)-TAN1251C. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Feb 26]. Available from: https://www.repository.cam.ac.uk/handle/1810/301779.

Council of Science Editors:

Reich D. A novel photocatalytic strategy for complex aliphatic amine synthesis and the total synthesis of alkaloids (−) FR901483 and (+)-TAN1251C. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/301779


University of Alberta

19. Malihi, Farzad. Studies towards the total synthesis of CP-225,917 and CP-263,114.

Degree: PhD, Department of Chemistry, 2012, University of Alberta

 This thesis describes advanced model studies directed to the synthesis of CP- 225,917 and CP-263,114, complex natural products that have been shown to inhibit enzymes… (more)

Subjects/Keywords: Total synthesis; CP-263,114; CP-225,917

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APA (6th Edition):

Malihi, F. (2012). Studies towards the total synthesis of CP-225,917 and CP-263,114. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/dr26xz79k

Chicago Manual of Style (16th Edition):

Malihi, Farzad. “Studies towards the total synthesis of CP-225,917 and CP-263,114.” 2012. Doctoral Dissertation, University of Alberta. Accessed February 26, 2020. https://era.library.ualberta.ca/files/dr26xz79k.

MLA Handbook (7th Edition):

Malihi, Farzad. “Studies towards the total synthesis of CP-225,917 and CP-263,114.” 2012. Web. 26 Feb 2020.

Vancouver:

Malihi F. Studies towards the total synthesis of CP-225,917 and CP-263,114. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Feb 26]. Available from: https://era.library.ualberta.ca/files/dr26xz79k.

Council of Science Editors:

Malihi F. Studies towards the total synthesis of CP-225,917 and CP-263,114. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/dr26xz79k


University of Alberta

20. Elford, Timothy. α-exo-Alkylidene γ-lactones and γ-lactams via 2-alkoxycarbonyl allylboronates: mechanistic studies, diversity-oriented synthesis and target-oriented synthesis.

Degree: PhD, Department of Chemistry, 2010, University of Alberta

 Allylboration reactions have been thoroughly utilized in organic chemistry since it was discovered that they could add in a nucleophilic fashion to aldehydes and ketones… (more)

Subjects/Keywords: total synthesis; catalysis; combinatorial chemistry; allylboration reaction

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APA (6th Edition):

Elford, T. (2010). α-exo-Alkylidene γ-lactones and γ-lactams via 2-alkoxycarbonyl allylboronates: mechanistic studies, diversity-oriented synthesis and target-oriented synthesis. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/9w0324052

Chicago Manual of Style (16th Edition):

Elford, Timothy. “α-exo-Alkylidene γ-lactones and γ-lactams via 2-alkoxycarbonyl allylboronates: mechanistic studies, diversity-oriented synthesis and target-oriented synthesis.” 2010. Doctoral Dissertation, University of Alberta. Accessed February 26, 2020. https://era.library.ualberta.ca/files/9w0324052.

MLA Handbook (7th Edition):

Elford, Timothy. “α-exo-Alkylidene γ-lactones and γ-lactams via 2-alkoxycarbonyl allylboronates: mechanistic studies, diversity-oriented synthesis and target-oriented synthesis.” 2010. Web. 26 Feb 2020.

Vancouver:

Elford T. α-exo-Alkylidene γ-lactones and γ-lactams via 2-alkoxycarbonyl allylboronates: mechanistic studies, diversity-oriented synthesis and target-oriented synthesis. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2020 Feb 26]. Available from: https://era.library.ualberta.ca/files/9w0324052.

Council of Science Editors:

Elford T. α-exo-Alkylidene γ-lactones and γ-lactams via 2-alkoxycarbonyl allylboronates: mechanistic studies, diversity-oriented synthesis and target-oriented synthesis. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/9w0324052


University of Minnesota

21. 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 (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 February 26, 2020. 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. 26 Feb 2020.

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 2020 Feb 26]. 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 Minnesota

22. Willoughby, Patrick. Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction.

Degree: Chemistry, 2013, University of Minnesota

 Part I: The salinosporamides are a subset of polyketide-derived marine natural products that have as their key structural feature a fused γ-lactam/β-lactone moiety. These molecules… (more)

Subjects/Keywords: Natural products; Synthetic methodology; Total synthesis; Chemistry

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APA (6th Edition):

Willoughby, P. (2013). Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction. (Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/167685

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):

Willoughby, Patrick. “Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction.” 2013. Thesis, University of Minnesota. Accessed February 26, 2020. http://hdl.handle.net/11299/167685.

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

MLA Handbook (7th Edition):

Willoughby, Patrick. “Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction.” 2013. Web. 26 Feb 2020.

Vancouver:

Willoughby P. Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction. [Internet] [Thesis]. University of Minnesota; 2013. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/11299/167685.

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

Council of Science Editors:

Willoughby P. Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction. [Thesis]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/167685

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


Rochester Institute of Technology

23. Rugg, Kyle. Studies Toward the Total Synthesis of Eletefine.

Degree: MS, School of Chemistry and Materials Science (COS), 2013, Rochester Institute of Technology

  Eletefine is a natural product of the stephaoxocane family of alkaloids. It possesses an isoquinoline moiety functionalized with three methoxy groups forming an electron… (more)

Subjects/Keywords: Des-hydroxyeletefine; Eletefine; Sonogashira; Stephaoxocane; Total synthesis

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APA (6th Edition):

Rugg, K. (2013). Studies Toward the Total Synthesis of Eletefine. (Masters Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/8150

Chicago Manual of Style (16th Edition):

Rugg, Kyle. “Studies Toward the Total Synthesis of Eletefine.” 2013. Masters Thesis, Rochester Institute of Technology. Accessed February 26, 2020. https://scholarworks.rit.edu/theses/8150.

MLA Handbook (7th Edition):

Rugg, Kyle. “Studies Toward the Total Synthesis of Eletefine.” 2013. Web. 26 Feb 2020.

Vancouver:

Rugg K. Studies Toward the Total Synthesis of Eletefine. [Internet] [Masters thesis]. Rochester Institute of Technology; 2013. [cited 2020 Feb 26]. Available from: https://scholarworks.rit.edu/theses/8150.

Council of Science Editors:

Rugg K. Studies Toward the Total Synthesis of Eletefine. [Masters Thesis]. Rochester Institute of Technology; 2013. Available from: https://scholarworks.rit.edu/theses/8150


University of Pennsylvania

24. Shvartsbart, Artem. Total Synthesis of (-)-Calyciphylline N.

Degree: 2014, University of Pennsylvania

 The dissertation herein describes the first total synthesis of the complex Daphniphyllum alkaloid, (-)-calyciphylline N. This alkaloid was chosen as the target in our synthetic… (more)

Subjects/Keywords: Alkaloids; Calyciphylline; Daphniphyllum; Total Synthesis; Organic Chemistry

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APA (6th Edition):

Shvartsbart, A. (2014). Total Synthesis of (-)-Calyciphylline N. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1442

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):

Shvartsbart, Artem. “Total Synthesis of (-)-Calyciphylline N.” 2014. Thesis, University of Pennsylvania. Accessed February 26, 2020. https://repository.upenn.edu/edissertations/1442.

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

MLA Handbook (7th Edition):

Shvartsbart, Artem. “Total Synthesis of (-)-Calyciphylline N.” 2014. Web. 26 Feb 2020.

Vancouver:

Shvartsbart A. Total Synthesis of (-)-Calyciphylline N. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2020 Feb 26]. Available from: https://repository.upenn.edu/edissertations/1442.

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

Council of Science Editors:

Shvartsbart A. Total Synthesis of (-)-Calyciphylline N. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1442

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


North Carolina State University

25. Cash, Brandon Michael. Advances in the Total Synthesis of Dihydrolycolucine.

Degree: PhD, Chemistry, 2010, North Carolina State University

 Dihydrolycolucine is a Lycopodium alkaloid that has gained attention over the recent years due to its complex architecture and potential medicinal value. In an effort… (more)

Subjects/Keywords: total synthesis; natural product; lycopodium; dihydropyridone; dihydrolycolucine

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APA (6th Edition):

Cash, B. M. (2010). Advances in the Total Synthesis of Dihydrolycolucine. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/3010

Chicago Manual of Style (16th Edition):

Cash, Brandon Michael. “Advances in the Total Synthesis of Dihydrolycolucine.” 2010. Doctoral Dissertation, North Carolina State University. Accessed February 26, 2020. http://www.lib.ncsu.edu/resolver/1840.16/3010.

MLA Handbook (7th Edition):

Cash, Brandon Michael. “Advances in the Total Synthesis of Dihydrolycolucine.” 2010. Web. 26 Feb 2020.

Vancouver:

Cash BM. Advances in the Total Synthesis of Dihydrolycolucine. [Internet] [Doctoral dissertation]. North Carolina State University; 2010. [cited 2020 Feb 26]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3010.

Council of Science Editors:

Cash BM. Advances in the Total Synthesis of Dihydrolycolucine. [Doctoral Dissertation]. North Carolina State University; 2010. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3010


University of Rochester

26. Malona, John A. (1981 - ). I. scandium (III) catalyzed Nazarov cyclization of heteroaryl-vinyl ketones : II. Efforts towards the total synthesis of (±) - rocaglamide via a Nazarov cyclization strategy ; III. Efforts towards the total synthesis of (±) - rocaglamide via an alkoxy allene epoxidation/Nazarov cyclization.

Degree: PhD, 2009, University of Rochester

 I. Scandium (III) Catalyzed Nazarov Cyclizations of Heteroaryl-Vinyl Ketones This chapter describes the successful development of a catalytic method for the Nazarov cyclization of heteroaryl-vinyl… (more)

Subjects/Keywords: Nazarov; Allene oxide; Total synthesis; Rocaglamide

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APA (6th Edition):

Malona, J. A. (. -. ). (2009). I. scandium (III) catalyzed Nazarov cyclization of heteroaryl-vinyl ketones : II. Efforts towards the total synthesis of (±) - rocaglamide via a Nazarov cyclization strategy ; III. Efforts towards the total synthesis of (±) - rocaglamide via an alkoxy allene epoxidation/Nazarov cyclization. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/7445

Chicago Manual of Style (16th Edition):

Malona, John A (1981 - ). “I. scandium (III) catalyzed Nazarov cyclization of heteroaryl-vinyl ketones : II. Efforts towards the total synthesis of (±) - rocaglamide via a Nazarov cyclization strategy ; III. Efforts towards the total synthesis of (±) - rocaglamide via an alkoxy allene epoxidation/Nazarov cyclization.” 2009. Doctoral Dissertation, University of Rochester. Accessed February 26, 2020. http://hdl.handle.net/1802/7445.

MLA Handbook (7th Edition):

Malona, John A (1981 - ). “I. scandium (III) catalyzed Nazarov cyclization of heteroaryl-vinyl ketones : II. Efforts towards the total synthesis of (±) - rocaglamide via a Nazarov cyclization strategy ; III. Efforts towards the total synthesis of (±) - rocaglamide via an alkoxy allene epoxidation/Nazarov cyclization.” 2009. Web. 26 Feb 2020.

Vancouver:

Malona JA(-). I. scandium (III) catalyzed Nazarov cyclization of heteroaryl-vinyl ketones : II. Efforts towards the total synthesis of (±) - rocaglamide via a Nazarov cyclization strategy ; III. Efforts towards the total synthesis of (±) - rocaglamide via an alkoxy allene epoxidation/Nazarov cyclization. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/1802/7445.

Council of Science Editors:

Malona JA(-). I. scandium (III) catalyzed Nazarov cyclization of heteroaryl-vinyl ketones : II. Efforts towards the total synthesis of (±) - rocaglamide via a Nazarov cyclization strategy ; III. Efforts towards the total synthesis of (±) - rocaglamide via an alkoxy allene epoxidation/Nazarov cyclization. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/7445


University of Rochester

27. Biegasiewicz, Kyle Francis (1988 - ). Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506.

Degree: PhD, 2017, University of Rochester

 Part I. Mechanistic Studies, Optimization, and Further Applications of the Organocatalytic α -Hydroxymethylation of Aldehydes: </br> Further developments in studies of the direct α-hydroymethylation of… (more)

Subjects/Keywords: FK-506; Hydroxymethylation; Organocatalysis; Total synthesis

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APA (6th Edition):

Biegasiewicz, K. F. (. -. ). (2017). Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/31893

Chicago Manual of Style (16th Edition):

Biegasiewicz, Kyle Francis (1988 - ). “Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506.” 2017. Doctoral Dissertation, University of Rochester. Accessed February 26, 2020. http://hdl.handle.net/1802/31893.

MLA Handbook (7th Edition):

Biegasiewicz, Kyle Francis (1988 - ). “Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506.” 2017. Web. 26 Feb 2020.

Vancouver:

Biegasiewicz KF(-). Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506. [Internet] [Doctoral dissertation]. University of Rochester; 2017. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/1802/31893.

Council of Science Editors:

Biegasiewicz KF(-). Part I. Mechanistic studies, optimization, and further applications of the organocatalytic α -hydroxymethylation of aldehydes ; Part II. Studies toward the total synthesis of FK-506. [Doctoral Dissertation]. University of Rochester; 2017. Available from: http://hdl.handle.net/1802/31893


Brock University

28. Varghese, Vimal. Chemoenzymatic Total Synthesis of Morphine alkaloids: Synthesis of Dihydrocodeine and Hydrocodone via a Double Claisen Strategy and ent-Hydromorphone via an Oxidative Dearomatization/intramolecular [4+2] Cycloaddition .

Degree: Department of Chemistry, 2015, Brock University

 This thesis describes the chemoenzymatic synthesis of three morphine alkaloids. The total synthesis of dihydrocodeine and hydrocodone was accomplished starting from bromobenzene in 16 and… (more)

Subjects/Keywords: Total synthesis; Chemoenzymatic; Natural product; Morphine alkaloids

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

APA (6th Edition):

Varghese, V. (2015). Chemoenzymatic Total Synthesis of Morphine alkaloids: Synthesis of Dihydrocodeine and Hydrocodone via a Double Claisen Strategy and ent-Hydromorphone via an Oxidative Dearomatization/intramolecular [4+2] Cycloaddition . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/5980

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):

Varghese, Vimal. “Chemoenzymatic Total Synthesis of Morphine alkaloids: Synthesis of Dihydrocodeine and Hydrocodone via a Double Claisen Strategy and ent-Hydromorphone via an Oxidative Dearomatization/intramolecular [4+2] Cycloaddition .” 2015. Thesis, Brock University. Accessed February 26, 2020. http://hdl.handle.net/10464/5980.

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

MLA Handbook (7th Edition):

Varghese, Vimal. “Chemoenzymatic Total Synthesis of Morphine alkaloids: Synthesis of Dihydrocodeine and Hydrocodone via a Double Claisen Strategy and ent-Hydromorphone via an Oxidative Dearomatization/intramolecular [4+2] Cycloaddition .” 2015. Web. 26 Feb 2020.

Vancouver:

Varghese V. Chemoenzymatic Total Synthesis of Morphine alkaloids: Synthesis of Dihydrocodeine and Hydrocodone via a Double Claisen Strategy and ent-Hydromorphone via an Oxidative Dearomatization/intramolecular [4+2] Cycloaddition . [Internet] [Thesis]. Brock University; 2015. [cited 2020 Feb 26]. Available from: http://hdl.handle.net/10464/5980.

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

Council of Science Editors:

Varghese V. Chemoenzymatic Total Synthesis of Morphine alkaloids: Synthesis of Dihydrocodeine and Hydrocodone via a Double Claisen Strategy and ent-Hydromorphone via an Oxidative Dearomatization/intramolecular [4+2] Cycloaddition . [Thesis]. Brock University; 2015. Available from: http://hdl.handle.net/10464/5980

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


Penn State University

29. Liu, Peng. TOTAL SYNTHESES OF (-)-SECU AMAMINE A.

Degree: PhD, Chemistry, 2010, Penn State University

 In part I, a convergent stereoselective total synthesis of the novel Securinega alkaloid (-)- secu’amamine A (9) was described. The synthesis requires 15 steps starting… (more)

Subjects/Keywords: communesin F; total synthesis; secuamamine A

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

APA (6th Edition):

Liu, P. (2010). TOTAL SYNTHESES OF (-)-SECU AMAMINE A. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11178

Chicago Manual of Style (16th Edition):

Liu, Peng. “TOTAL SYNTHESES OF (-)-SECU AMAMINE A.” 2010. Doctoral Dissertation, Penn State University. Accessed February 26, 2020. https://etda.libraries.psu.edu/catalog/11178.

MLA Handbook (7th Edition):

Liu, Peng. “TOTAL SYNTHESES OF (-)-SECU AMAMINE A.” 2010. Web. 26 Feb 2020.

Vancouver:

Liu P. TOTAL SYNTHESES OF (-)-SECU AMAMINE A. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2020 Feb 26]. Available from: https://etda.libraries.psu.edu/catalog/11178.

Council of Science Editors:

Liu P. TOTAL SYNTHESES OF (-)-SECU AMAMINE A. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11178


Penn State University

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

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 February 26, 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. 26 Feb 2020.

Vancouver:

Nocket AJ. Total Synthesis of the Tetracyclic Antimalarial Alkaloid (±)-myrioneurinol. [Internet] [Doctoral dissertation]. Penn State University; 2015. [cited 2020 Feb 26]. 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

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