Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(nitrone). Showing records 1 – 27 of 27 total matches.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


Kwame Nkrumah University of Science and Technology

1. Opoku, Ernest; Arhin, Grace; Pipim, George Baffour; Adams, Anita Houston; Tia, Richard. Site‑, enantio‑ and stereo‑selectivities of the 1,3‑dipolar cycloaddition reactions of oxanorbornadiene with C,N‑disubstituted nitrones and dimethyl nitrilimines: a DFT mechanistic study.

Degree: 2020, Kwame Nkrumah University of Science and Technology

1,3-Dipolar cycloaddition of nitrones to oxanorbornadienes is an important method for the enantioselective synthesis of highly substituted 5-membered heterocycles such as furans and isoxazolidines, which… (more)

Subjects/Keywords: Dipole; Oxanorbornadiene; Nitrone; Enantioselectivity; Density functional theory

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Opoku, Ernest; Arhin, Grace; Pipim, George Baffour; Adams, Anita Houston; Tia, R. (2020). Site‑, enantio‑ and stereo‑selectivities of the 1,3‑dipolar cycloaddition reactions of oxanorbornadiene with C,N‑disubstituted nitrones and dimethyl nitrilimines: a DFT mechanistic study. (Thesis). Kwame Nkrumah University of Science and Technology. Retrieved from Theoretical Chemistry Accounts (2020) 139:16 https://doi.org/10.1007/s00214-019-2529-8 ; http://dspace.knust.edu.gh:8080/jspui/handle/123456789/12659

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):

Opoku, Ernest; Arhin, Grace; Pipim, George Baffour; Adams, Anita Houston; Tia, Richard. “Site‑, enantio‑ and stereo‑selectivities of the 1,3‑dipolar cycloaddition reactions of oxanorbornadiene with C,N‑disubstituted nitrones and dimethyl nitrilimines: a DFT mechanistic study.” 2020. Thesis, Kwame Nkrumah University of Science and Technology. Accessed May 09, 2021. Theoretical Chemistry Accounts (2020) 139:16 https://doi.org/10.1007/s00214-019-2529-8 ; http://dspace.knust.edu.gh:8080/jspui/handle/123456789/12659.

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

MLA Handbook (7th Edition):

Opoku, Ernest; Arhin, Grace; Pipim, George Baffour; Adams, Anita Houston; Tia, Richard. “Site‑, enantio‑ and stereo‑selectivities of the 1,3‑dipolar cycloaddition reactions of oxanorbornadiene with C,N‑disubstituted nitrones and dimethyl nitrilimines: a DFT mechanistic study.” 2020. Web. 09 May 2021.

Vancouver:

Opoku, Ernest; Arhin, Grace; Pipim, George Baffour; Adams, Anita Houston; Tia R. Site‑, enantio‑ and stereo‑selectivities of the 1,3‑dipolar cycloaddition reactions of oxanorbornadiene with C,N‑disubstituted nitrones and dimethyl nitrilimines: a DFT mechanistic study. [Internet] [Thesis]. Kwame Nkrumah University of Science and Technology; 2020. [cited 2021 May 09]. Available from: Theoretical Chemistry Accounts (2020) 139:16 https://doi.org/10.1007/s00214-019-2529-8 ; http://dspace.knust.edu.gh:8080/jspui/handle/123456789/12659.

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

Council of Science Editors:

Opoku, Ernest; Arhin, Grace; Pipim, George Baffour; Adams, Anita Houston; Tia R. Site‑, enantio‑ and stereo‑selectivities of the 1,3‑dipolar cycloaddition reactions of oxanorbornadiene with C,N‑disubstituted nitrones and dimethyl nitrilimines: a DFT mechanistic study. [Thesis]. Kwame Nkrumah University of Science and Technology; 2020. Available from: Theoretical Chemistry Accounts (2020) 139:16 https://doi.org/10.1007/s00214-019-2529-8 ; http://dspace.knust.edu.gh:8080/jspui/handle/123456789/12659

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


University of Colorado

2. Michael, Ryan Edward. New Methods for the Synthesis of All-Carbon Quaternary Centers via the Reactions of N-Vinyl Nitrones and Phenyl Hydrazines with Ketenes.

Degree: PhD, Chemistry & Biochemistry, 2013, University of Colorado

  This dissertation describes the development of new cascade reactions for the synthesis of quaternary carbons bearing additional proximal hindrance. The general reaction design principles… (more)

Subjects/Keywords: N-vinyl nitrone; pericyclic cascade reaction; Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Michael, R. E. (2013). New Methods for the Synthesis of All-Carbon Quaternary Centers via the Reactions of N-Vinyl Nitrones and Phenyl Hydrazines with Ketenes. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/100

Chicago Manual of Style (16th Edition):

Michael, Ryan Edward. “New Methods for the Synthesis of All-Carbon Quaternary Centers via the Reactions of N-Vinyl Nitrones and Phenyl Hydrazines with Ketenes.” 2013. Doctoral Dissertation, University of Colorado. Accessed May 09, 2021. https://scholar.colorado.edu/chem_gradetds/100.

MLA Handbook (7th Edition):

Michael, Ryan Edward. “New Methods for the Synthesis of All-Carbon Quaternary Centers via the Reactions of N-Vinyl Nitrones and Phenyl Hydrazines with Ketenes.” 2013. Web. 09 May 2021.

Vancouver:

Michael RE. New Methods for the Synthesis of All-Carbon Quaternary Centers via the Reactions of N-Vinyl Nitrones and Phenyl Hydrazines with Ketenes. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2021 May 09]. Available from: https://scholar.colorado.edu/chem_gradetds/100.

Council of Science Editors:

Michael RE. New Methods for the Synthesis of All-Carbon Quaternary Centers via the Reactions of N-Vinyl Nitrones and Phenyl Hydrazines with Ketenes. [Doctoral Dissertation]. University of Colorado; 2013. Available from: https://scholar.colorado.edu/chem_gradetds/100

3. Rosselin, Marie. Design of amphiphilic nitrones with improved spin-trapping and antioxidant properties : Conception de nitrones amphiphiles aux propriétés de piégeage et antioxydantes supérieure.

Degree: Docteur es, Chimie organique, 2014, Avignon

Le stress oxydant se définit comme un déséquilibre entre la production d’espèces oxygénées et azotés réactives et les défenses antioxydants. Ce phénomène est associé à… (more)

Subjects/Keywords: Amphiphilie; Stress oxydant; Nitrone; Antioxydant; Espèces oxygénées réactives; Reactive oxygen species; Oxidative stress; Nitrone; Amphiphily; Antioxidant; 570; 610

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rosselin, M. (2014). Design of amphiphilic nitrones with improved spin-trapping and antioxidant properties : Conception de nitrones amphiphiles aux propriétés de piégeage et antioxydantes supérieure. (Doctoral Dissertation). Avignon. Retrieved from http://www.theses.fr/2014AVIG0258

Chicago Manual of Style (16th Edition):

Rosselin, Marie. “Design of amphiphilic nitrones with improved spin-trapping and antioxidant properties : Conception de nitrones amphiphiles aux propriétés de piégeage et antioxydantes supérieure.” 2014. Doctoral Dissertation, Avignon. Accessed May 09, 2021. http://www.theses.fr/2014AVIG0258.

MLA Handbook (7th Edition):

Rosselin, Marie. “Design of amphiphilic nitrones with improved spin-trapping and antioxidant properties : Conception de nitrones amphiphiles aux propriétés de piégeage et antioxydantes supérieure.” 2014. Web. 09 May 2021.

Vancouver:

Rosselin M. Design of amphiphilic nitrones with improved spin-trapping and antioxidant properties : Conception de nitrones amphiphiles aux propriétés de piégeage et antioxydantes supérieure. [Internet] [Doctoral dissertation]. Avignon; 2014. [cited 2021 May 09]. Available from: http://www.theses.fr/2014AVIG0258.

Council of Science Editors:

Rosselin M. Design of amphiphilic nitrones with improved spin-trapping and antioxidant properties : Conception de nitrones amphiphiles aux propriétés de piégeage et antioxydantes supérieure. [Doctoral Dissertation]. Avignon; 2014. Available from: http://www.theses.fr/2014AVIG0258


Texas A&M University

4. Huehls, Christopher Bryan. Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes.

Degree: PhD, Chemistry, 2014, Texas A&M University

 Indole-containing structures and their generation still draw much attention because of their ubiquity in natural products, medicinal compounds, and organic materials. Given this prevalence, synthetic… (more)

Subjects/Keywords: indole; indolenine; nitrone; pyrroloindoline; hydrocarbazole; conjugate addition; iron; amination; hydroamination

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Huehls, C. B. (2014). Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152597

Chicago Manual of Style (16th Edition):

Huehls, Christopher Bryan. “Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes.” 2014. Doctoral Dissertation, Texas A&M University. Accessed May 09, 2021. http://hdl.handle.net/1969.1/152597.

MLA Handbook (7th Edition):

Huehls, Christopher Bryan. “Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes.” 2014. Web. 09 May 2021.

Vancouver:

Huehls CB. Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/1969.1/152597.

Council of Science Editors:

Huehls CB. Novel Methodology Towards the Indole Core and Iron-Catalyzed Electrophilic Hydroamination of Alkenes. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152597


Colorado State University

5. Smith, Genessa M. Progress toward the total synthesis of citrinadins A and B.

Degree: PhD, Chemistry, 2012, Colorado State University

 In 2005 Kobayashi reported the isolation and absolute stereochemistry of Citrinadin A (1) and Citrinadin B (2), novel secondary metabolites of the marine fungus Penicillium… (more)

Subjects/Keywords: (3+2) dipolar cycloaddition; nitrone; Citrinadin B; Citrinadin A

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Smith, G. M. (2012). Progress toward the total synthesis of citrinadins A and B. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/67651

Chicago Manual of Style (16th Edition):

Smith, Genessa M. “Progress toward the total synthesis of citrinadins A and B.” 2012. Doctoral Dissertation, Colorado State University. Accessed May 09, 2021. http://hdl.handle.net/10217/67651.

MLA Handbook (7th Edition):

Smith, Genessa M. “Progress toward the total synthesis of citrinadins A and B.” 2012. Web. 09 May 2021.

Vancouver:

Smith GM. Progress toward the total synthesis of citrinadins A and B. [Internet] [Doctoral dissertation]. Colorado State University; 2012. [cited 2021 May 09]. Available from: http://hdl.handle.net/10217/67651.

Council of Science Editors:

Smith GM. Progress toward the total synthesis of citrinadins A and B. [Doctoral Dissertation]. Colorado State University; 2012. Available from: http://hdl.handle.net/10217/67651


University of Melbourne

6. Johnson, Brian A. Synthesis of histrionicotoxin analogues using coventional and continuous flow approaches.

Degree: 2011, University of Melbourne

 The histrionicotoxins are a family of alkaloids, originally isolated from the skin extracts of the amphibian Dendrobatidae histrionicus, that display non-competitive inhibition of the nicotinic… (more)

Subjects/Keywords: alkaloids; histrionicotoxin; analogues; continuous flow; synthesis; nitrone dipolar cycloadditions

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Johnson, B. A. (2011). Synthesis of histrionicotoxin analogues using coventional and continuous flow approaches. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/36699

Chicago Manual of Style (16th Edition):

Johnson, Brian A. “Synthesis of histrionicotoxin analogues using coventional and continuous flow approaches.” 2011. Doctoral Dissertation, University of Melbourne. Accessed May 09, 2021. http://hdl.handle.net/11343/36699.

MLA Handbook (7th Edition):

Johnson, Brian A. “Synthesis of histrionicotoxin analogues using coventional and continuous flow approaches.” 2011. Web. 09 May 2021.

Vancouver:

Johnson BA. Synthesis of histrionicotoxin analogues using coventional and continuous flow approaches. [Internet] [Doctoral dissertation]. University of Melbourne; 2011. [cited 2021 May 09]. Available from: http://hdl.handle.net/11343/36699.

Council of Science Editors:

Johnson BA. Synthesis of histrionicotoxin analogues using coventional and continuous flow approaches. [Doctoral Dissertation]. University of Melbourne; 2011. Available from: http://hdl.handle.net/11343/36699


University of Illinois – Chicago

7. Dimitra Kontokosta (1909459). The Versatile Reactivity of Oximes with Vinyl Boronic Acids and Development of 4-Phosphono-β-Lactams.

Degree: 2014, University of Illinois – Chicago

 The tunable reactivity of oximes with alkenyl boronic acids towards C–O versus C–N bond formation has been explored. O-alkenyl oximes have been evaluated as precursors… (more)

Subjects/Keywords: Uncategorized; benzophenone oxime; alkenyl boronic acid; [1,3] rearrangement; vinyl nitrone

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

(1909459), D. K. (2014). The Versatile Reactivity of Oximes with Vinyl Boronic Acids and Development of 4-Phosphono-β-Lactams. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/11219

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):

(1909459), Dimitra Kontokosta. “The Versatile Reactivity of Oximes with Vinyl Boronic Acids and Development of 4-Phosphono-β-Lactams.” 2014. Thesis, University of Illinois – Chicago. Accessed May 09, 2021. http://hdl.handle.net/10027/11219.

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

MLA Handbook (7th Edition):

(1909459), Dimitra Kontokosta. “The Versatile Reactivity of Oximes with Vinyl Boronic Acids and Development of 4-Phosphono-β-Lactams.” 2014. Web. 09 May 2021.

Vancouver:

(1909459) DK. The Versatile Reactivity of Oximes with Vinyl Boronic Acids and Development of 4-Phosphono-β-Lactams. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/10027/11219.

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

Council of Science Editors:

(1909459) DK. The Versatile Reactivity of Oximes with Vinyl Boronic Acids and Development of 4-Phosphono-β-Lactams. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/11219

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


Université de Grenoble

8. Boisson, Julien. Synthèse de nouveaux iminosucres et évaluation de leur activité inhibitrice de glycosidases : Synthesis of new iminosugar and evaluation of their inhibitory activity to glycosidase.

Degree: Docteur es, Chimie organique, 2014, Université de Grenoble

Le travail présenté dans ce manuscrit concerne la synthèse et une évaluation biologique de 10 nouveaux iminosucres. Les iminosucres sont une classe importante d'inhibiteurs de… (more)

Subjects/Keywords: Iminosucres; Nitrone; Chimie organique; Réaction de métathèse cyclisante; Inhibiteur; Activité biologique; Iminosugars; Nitrone; Organic chemistry; Ring closing metathesis; Inhibitor; Biological activity; 540

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Boisson, J. (2014). Synthèse de nouveaux iminosucres et évaluation de leur activité inhibitrice de glycosidases : Synthesis of new iminosugar and evaluation of their inhibitory activity to glycosidase. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2014GRENV027

Chicago Manual of Style (16th Edition):

Boisson, Julien. “Synthèse de nouveaux iminosucres et évaluation de leur activité inhibitrice de glycosidases : Synthesis of new iminosugar and evaluation of their inhibitory activity to glycosidase.” 2014. Doctoral Dissertation, Université de Grenoble. Accessed May 09, 2021. http://www.theses.fr/2014GRENV027.

MLA Handbook (7th Edition):

Boisson, Julien. “Synthèse de nouveaux iminosucres et évaluation de leur activité inhibitrice de glycosidases : Synthesis of new iminosugar and evaluation of their inhibitory activity to glycosidase.” 2014. Web. 09 May 2021.

Vancouver:

Boisson J. Synthèse de nouveaux iminosucres et évaluation de leur activité inhibitrice de glycosidases : Synthesis of new iminosugar and evaluation of their inhibitory activity to glycosidase. [Internet] [Doctoral dissertation]. Université de Grenoble; 2014. [cited 2021 May 09]. Available from: http://www.theses.fr/2014GRENV027.

Council of Science Editors:

Boisson J. Synthèse de nouveaux iminosucres et évaluation de leur activité inhibitrice de glycosidases : Synthesis of new iminosugar and evaluation of their inhibitory activity to glycosidase. [Doctoral Dissertation]. Université de Grenoble; 2014. Available from: http://www.theses.fr/2014GRENV027


Texas A&M University

9. Kang, Jun Yong. Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene.

Degree: MS, Chemistry, 2010, Texas A&M University

 A new synthetic method toward 5-substituted isoxazolidines by [3 plus 2] cycloaddition of nitrones generated from nitrosobenzene and styrene was discovered. The formation of nitrones… (more)

Subjects/Keywords: [3+2] dipolar cycloaddition; isoxazolidine; nitrone

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kang, J. Y. (2010). Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82

Chicago Manual of Style (16th Edition):

Kang, Jun Yong. “Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene.” 2010. Masters Thesis, Texas A&M University. Accessed May 09, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82.

MLA Handbook (7th Edition):

Kang, Jun Yong. “Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene.” 2010. Web. 09 May 2021.

Vancouver:

Kang JY. Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene. [Internet] [Masters thesis]. Texas A&M University; 2010. [cited 2021 May 09]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82.

Council of Science Editors:

Kang JY. Synthesis of 5-Substituted Isoxazolidines by [3 plus 2] Cycloaddition of Nitrones Generated in an Unusual Way from Nitrosobenzene and Styrene. [Masters Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2008-12-82


University of Illinois – Chicago

10. Tyler W Reidl (8973620). Exploitation of Nitrone and Hydroxylamine N–O Bonds for the Construction of Functionalized Heterocycles.

Degree: 2019, University of Illinois – Chicago

 In the Anderson group at UIC, we aim to develop new transformations involving N-vinylnitrone and N,O-divinylhydroxylamine intermediates to access functionalized molecules and novel heterocyclic scaffolds… (more)

Subjects/Keywords: Uncategorized; Nitrone; pyrroline; azetidine; cycloaddition; cascade; asymmetric; catalysis; rearrangement; alkyne; allene; tetrahydrofuran

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

(8973620), T. W. R. (2019). Exploitation of Nitrone and Hydroxylamine N–O Bonds for the Construction of Functionalized Heterocycles. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10.25417/uic.12481601.v1

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):

(8973620), Tyler W Reidl. “Exploitation of Nitrone and Hydroxylamine N–O Bonds for the Construction of Functionalized Heterocycles.” 2019. Thesis, University of Illinois – Chicago. Accessed May 09, 2021. http://hdl.handle.net/10.25417/uic.12481601.v1.

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

MLA Handbook (7th Edition):

(8973620), Tyler W Reidl. “Exploitation of Nitrone and Hydroxylamine N–O Bonds for the Construction of Functionalized Heterocycles.” 2019. Web. 09 May 2021.

Vancouver:

(8973620) TWR. Exploitation of Nitrone and Hydroxylamine N–O Bonds for the Construction of Functionalized Heterocycles. [Internet] [Thesis]. University of Illinois – Chicago; 2019. [cited 2021 May 09]. Available from: http://hdl.handle.net/10.25417/uic.12481601.v1.

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

Council of Science Editors:

(8973620) TWR. Exploitation of Nitrone and Hydroxylamine N–O Bonds for the Construction of Functionalized Heterocycles. [Thesis]. University of Illinois – Chicago; 2019. Available from: http://hdl.handle.net/10.25417/uic.12481601.v1

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


University of Toledo Health Science Campus

11. Nash, Kevin Michael. Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke.

Degree: PhD, Experimental Therapeutics, 2017, University of Toledo Health Science Campus

 Ischemic stroke is caused by a blockage of the blood flow to the brain resulting in neuronal and glial hypoxia leading to inflammatory and free… (more)

Subjects/Keywords: Pharmacology; Biochemistry; Neurobiology; Neurosciences; Organic Chemistry; Physical Chemistry; Nitrone; Reactive Oxygen Species; Nitric Oxide; Nitric Oxide Synthase; Stroke; Ischemia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nash, K. M. (2017). Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1512053682446096

Chicago Manual of Style (16th Edition):

Nash, Kevin Michael. “Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke.” 2017. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed May 09, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=mco1512053682446096.

MLA Handbook (7th Edition):

Nash, Kevin Michael. “Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke.” 2017. Web. 09 May 2021.

Vancouver:

Nash KM. Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2017. [cited 2021 May 09]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1512053682446096.

Council of Science Editors:

Nash KM. Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1512053682446096

12. Shpak-Kraievskyi, Pavlo. Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition.

Degree: Docteur es, Chimie fine, 2013, Le Mans

Les peptides aldéhydes sont connus comme inhibiteurs de protéases et précurseurs de différentes classes de composés biologiquement actifs. Les méthodes pour leur synthèse impliquent classiquement… (more)

Subjects/Keywords: Β-aminoaldéhyde; Épimérisation; Synthèse peptidique; Oxazinone; 6-ATO; Transacétalisation; Cycloaddition dipolaire-1,3; Nitrone; Isoxazolidine; Stéréosélective; Organocatalyseur; Couplage peptidique encombré; Β-aminoaldehyde; Epimerisation; Peptide synthesis; Oxazinone; 6-ATO; Transacetalisation; 1,3-dipolar cycloaddition; Nitrone; Isoxazolidine; Stereoselective; Organocatalyst; Hindered peptide coupling

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shpak-Kraievskyi, P. (2013). Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition. (Doctoral Dissertation). Le Mans. Retrieved from http://www.theses.fr/2013LEMA1002

Chicago Manual of Style (16th Edition):

Shpak-Kraievskyi, Pavlo. “Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition.” 2013. Doctoral Dissertation, Le Mans. Accessed May 09, 2021. http://www.theses.fr/2013LEMA1002.

MLA Handbook (7th Edition):

Shpak-Kraievskyi, Pavlo. “Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition.” 2013. Web. 09 May 2021.

Vancouver:

Shpak-Kraievskyi P. Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition. [Internet] [Doctoral dissertation]. Le Mans; 2013. [cited 2021 May 09]. Available from: http://www.theses.fr/2013LEMA1002.

Council of Science Editors:

Shpak-Kraievskyi P. Nouvelles méthodologies pour la synthèse asymétrique de peptides aldéhydiques β3-C-terminaux et de dérivés d’acides aminés disubstitués via hétérocycloaddition : New methodologies for the asymmetric synthesis of peptides β3-cterminal aldehydes and disubstituted amino acid derivatives via heterocycloaddition. [Doctoral Dissertation]. Le Mans; 2013. Available from: http://www.theses.fr/2013LEMA1002


Indian Institute of Science

13. Gorla, Suresh Kumar. Structure And Reactivity In Bridged Polycylic Systems : Cis-trans Enantiomerism, Fulvene Cycloadditions And Crystallographic Studies Of Bridgehead β-Ketoacids.

Degree: PhD, Faculty of Science, 2011, Indian Institute of Science

 The thesis entitled "Structure and reactivity in bridged polycyclic systems: cis-trans enantiomerism, fulvene cycloadditions and crystallographic studies of bridgehead β-ketoacids " consists of two parts.… (more)

Subjects/Keywords: Ketones; Beta-Ketoacids; Polycyclic System; Fulvenes; Enantiomers; Amines; Amino Acids; Ring Formation (Chemistry); β-ketoacids; Diels-Alder Cycloadducts; Fulvene-nitrone Cycloadditions; Organic Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gorla, S. K. (2011). Structure And Reactivity In Bridged Polycylic Systems : Cis-trans Enantiomerism, Fulvene Cycloadditions And Crystallographic Studies Of Bridgehead β-Ketoacids. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/1074

Chicago Manual of Style (16th Edition):

Gorla, Suresh Kumar. “Structure And Reactivity In Bridged Polycylic Systems : Cis-trans Enantiomerism, Fulvene Cycloadditions And Crystallographic Studies Of Bridgehead β-Ketoacids.” 2011. Doctoral Dissertation, Indian Institute of Science. Accessed May 09, 2021. http://etd.iisc.ac.in/handle/2005/1074.

MLA Handbook (7th Edition):

Gorla, Suresh Kumar. “Structure And Reactivity In Bridged Polycylic Systems : Cis-trans Enantiomerism, Fulvene Cycloadditions And Crystallographic Studies Of Bridgehead β-Ketoacids.” 2011. Web. 09 May 2021.

Vancouver:

Gorla SK. Structure And Reactivity In Bridged Polycylic Systems : Cis-trans Enantiomerism, Fulvene Cycloadditions And Crystallographic Studies Of Bridgehead β-Ketoacids. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2011. [cited 2021 May 09]. Available from: http://etd.iisc.ac.in/handle/2005/1074.

Council of Science Editors:

Gorla SK. Structure And Reactivity In Bridged Polycylic Systems : Cis-trans Enantiomerism, Fulvene Cycloadditions And Crystallographic Studies Of Bridgehead β-Ketoacids. [Doctoral Dissertation]. Indian Institute of Science; 2011. Available from: http://etd.iisc.ac.in/handle/2005/1074

14. Hamdi, Abdelrahman. Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique.

Degree: Docteur es, Chimie organique, 2020, Le Mans; Université de Mansoura

L’’ infection par le virus de l’ hépatite C (HCV) est considérée comme un des défis majeurs de santé publique en Egypte où la prévalence… (more)

Subjects/Keywords: Hépatite C; Ether vinylique; Nitrone; Réaction 1,3-dipolaire; Isoxazolidine; Allylation; Analogues de l’asunaprévir; HCV NS 3/4A; Hepatitis C; Vinyl ether; 1,3-DC reaction; Asunaprevir analogues; 547.59

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hamdi, A. (2020). Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique. (Doctoral Dissertation). Le Mans; Université de Mansoura. Retrieved from http://www.theses.fr/2020LEMA1020

Chicago Manual of Style (16th Edition):

Hamdi, Abdelrahman. “Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique.” 2020. Doctoral Dissertation, Le Mans; Université de Mansoura. Accessed May 09, 2021. http://www.theses.fr/2020LEMA1020.

MLA Handbook (7th Edition):

Hamdi, Abdelrahman. “Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique.” 2020. Web. 09 May 2021.

Vancouver:

Hamdi A. Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique. [Internet] [Doctoral dissertation]. Le Mans; Université de Mansoura; 2020. [cited 2021 May 09]. Available from: http://www.theses.fr/2020LEMA1020.

Council of Science Editors:

Hamdi A. Asymmetric Synthesis of Oxaproline-Based Tripeptides Analogs of Asunaprevir and their Biological Evaluations : Synthèse asymétrique d’analogues tripeptidiques de l’asunaprévir basés sur une oxaproline et leur évaluation biologique. [Doctoral Dissertation]. Le Mans; Université de Mansoura; 2020. Available from: http://www.theses.fr/2020LEMA1020


ETH Zürich

15. Gygax, Peter. Beitrag zur Chemie der α-Chlornitrone.

Degree: 1977, ETH Zürich

Subjects/Keywords: NITRONE (ORGANISCHE CHEMIE); NITRONES (ORGANIC CHEMISTRY); info:eu-repo/classification/ddc/540; Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gygax, P. (1977). Beitrag zur Chemie der α-Chlornitrone. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/135661

Chicago Manual of Style (16th Edition):

Gygax, Peter. “Beitrag zur Chemie der α-Chlornitrone.” 1977. Doctoral Dissertation, ETH Zürich. Accessed May 09, 2021. http://hdl.handle.net/20.500.11850/135661.

MLA Handbook (7th Edition):

Gygax, Peter. “Beitrag zur Chemie der α-Chlornitrone.” 1977. Web. 09 May 2021.

Vancouver:

Gygax P. Beitrag zur Chemie der α-Chlornitrone. [Internet] [Doctoral dissertation]. ETH Zürich; 1977. [cited 2021 May 09]. Available from: http://hdl.handle.net/20.500.11850/135661.

Council of Science Editors:

Gygax P. Beitrag zur Chemie der α-Chlornitrone. [Doctoral Dissertation]. ETH Zürich; 1977. Available from: http://hdl.handle.net/20.500.11850/135661

16. Tiago Luiz Lopes. Modificação do produto natural (-)-∝- Bisabolol.

Degree: 2010, University of São Paulo

O (-)-?-bisabolol é um produto natural abundante no Brasil. É extraído de várias espécies de plantas. Possui atividades biológicas reconhecidas, que o torna extremamente interessante… (more)

Subjects/Keywords: Bisabolol; Cicloadição; Ciclopropanação; Nitronas; Oxidação; Bisabolol; Cycloaddition; Cyclopropanation; Nitrone; Oxidation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lopes, T. L. (2010). Modificação do produto natural (-)-∝- Bisabolol. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/97/97136/tde-22082013-112422/

Chicago Manual of Style (16th Edition):

Lopes, Tiago Luiz. “Modificação do produto natural (-)-∝- Bisabolol.” 2010. Masters Thesis, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/97/97136/tde-22082013-112422/.

MLA Handbook (7th Edition):

Lopes, Tiago Luiz. “Modificação do produto natural (-)-∝- Bisabolol.” 2010. Web. 09 May 2021.

Vancouver:

Lopes TL. Modificação do produto natural (-)-∝- Bisabolol. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/97/97136/tde-22082013-112422/.

Council of Science Editors:

Lopes TL. Modificação do produto natural (-)-∝- Bisabolol. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/97/97136/tde-22082013-112422/

17. Ben Ayed Achich, Kawther. Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones.

Degree: Docteur es, Chimie organique, 2016, Le Mans; Université de Sfax (Tunisie)

Lors de ces travaux de thèse, nous nous sommes intéressés au développement de deux voies différentes de cycloaddition dipolaire-1,3 (CD-1,3) asymétrique pour accéder à des… (more)

Subjects/Keywords: Synthèse asymétrique; Cycloaddition dipolaire 1,3; Nitrone; Isoxazolidine; Dipolarophile; Ether vinylique chiral; Enal; Isoxazoline; Asymmetric synthesis; Cycloaddition 1,3 dipolar; Chiral vinyl ether; 547.037

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ben Ayed Achich, K. (2016). Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones. (Doctoral Dissertation). Le Mans; Université de Sfax (Tunisie). Retrieved from http://www.theses.fr/2016LEMA1013

Chicago Manual of Style (16th Edition):

Ben Ayed Achich, Kawther. “Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones.” 2016. Doctoral Dissertation, Le Mans; Université de Sfax (Tunisie). Accessed May 09, 2021. http://www.theses.fr/2016LEMA1013.

MLA Handbook (7th Edition):

Ben Ayed Achich, Kawther. “Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones.” 2016. Web. 09 May 2021.

Vancouver:

Ben Ayed Achich K. Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones. [Internet] [Doctoral dissertation]. Le Mans; Université de Sfax (Tunisie); 2016. [cited 2021 May 09]. Available from: http://www.theses.fr/2016LEMA1013.

Council of Science Editors:

Ben Ayed Achich K. Synthèse énantiosélective d'aminoacides disubstitués polyfonctionnels via cycloaddition dipolaire d'α-carboxy cétonitrones : Enantioselective synthesis of polyfunctionnal amino acids by 1,3 dipolar cycloaddition via α-carboxy ketonitrones. [Doctoral Dissertation]. Le Mans; Université de Sfax (Tunisie); 2016. Available from: http://www.theses.fr/2016LEMA1013

18. Zaki, Mohamed. Réactivité et hémisynthèse des constituants majoritaires, de type eudesmanes, contenus dans des extraits de Dittrichia Viscosa : Reactivity and hemisynthesis of major constituents type eudesmanes contained in the extracts of Dittrichia Viscosa.

Degree: Docteur es, Chimie organique, 2015, Orléans; Université Hassan II (Casablanca, Maroc)

Au cours de ces dernières années, les sesquiterpénoïdes de type eudesmane et leurs activités biologiques font l'objet de nombreuses études phytochimiques et pharmacologiques, ainsi que… (more)

Subjects/Keywords: Dittrichia Viscosa; Hemisynthèse; Eudesmane; Acide α-costique; Acide ilicique; Tomentosine; Catalyse acide; Couplage de Heck; Addition nucléophile; Addition 1,3 dipolaire; Click chemistry; Nitrone; Oxyde de nitrile; Dittrichia Viscosa; Semisynthetic; Eudesmane; Α-costic acid; Ilicic acid; Tomentosin; Acid catalysis; Heck coupling; Nucleophilic addition; 1,3-dipolar addition; Click chemistry; Nitrone; Nitrile oxide; 547

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zaki, M. (2015). Réactivité et hémisynthèse des constituants majoritaires, de type eudesmanes, contenus dans des extraits de Dittrichia Viscosa : Reactivity and hemisynthesis of major constituents type eudesmanes contained in the extracts of Dittrichia Viscosa. (Doctoral Dissertation). Orléans; Université Hassan II (Casablanca, Maroc). Retrieved from http://www.theses.fr/2015ORLE2014

Chicago Manual of Style (16th Edition):

Zaki, Mohamed. “Réactivité et hémisynthèse des constituants majoritaires, de type eudesmanes, contenus dans des extraits de Dittrichia Viscosa : Reactivity and hemisynthesis of major constituents type eudesmanes contained in the extracts of Dittrichia Viscosa.” 2015. Doctoral Dissertation, Orléans; Université Hassan II (Casablanca, Maroc). Accessed May 09, 2021. http://www.theses.fr/2015ORLE2014.

MLA Handbook (7th Edition):

Zaki, Mohamed. “Réactivité et hémisynthèse des constituants majoritaires, de type eudesmanes, contenus dans des extraits de Dittrichia Viscosa : Reactivity and hemisynthesis of major constituents type eudesmanes contained in the extracts of Dittrichia Viscosa.” 2015. Web. 09 May 2021.

Vancouver:

Zaki M. Réactivité et hémisynthèse des constituants majoritaires, de type eudesmanes, contenus dans des extraits de Dittrichia Viscosa : Reactivity and hemisynthesis of major constituents type eudesmanes contained in the extracts of Dittrichia Viscosa. [Internet] [Doctoral dissertation]. Orléans; Université Hassan II (Casablanca, Maroc); 2015. [cited 2021 May 09]. Available from: http://www.theses.fr/2015ORLE2014.

Council of Science Editors:

Zaki M. Réactivité et hémisynthèse des constituants majoritaires, de type eudesmanes, contenus dans des extraits de Dittrichia Viscosa : Reactivity and hemisynthesis of major constituents type eudesmanes contained in the extracts of Dittrichia Viscosa. [Doctoral Dissertation]. Orléans; Université Hassan II (Casablanca, Maroc); 2015. Available from: http://www.theses.fr/2015ORLE2014

19. Chigrinova, Mariya. Development of New Bioorthogonal Strain-Promoted Alkyne-Nitrone Cycloaddition Methodology for Applications in Living Systems .

Degree: 2014, University of Ottawa

 Nitrones are alternatives to azides in rapid strain-promoted 1,3-dipolar cycloadditions with cyclooctynes. To evaluate the differences between nitrones and azides we have performed kinetic studies… (more)

Subjects/Keywords: Bioorthogonal; Strain-promoted; Alkyne; Nitrone; Cycloaddition; Kinetic; Biarylazacyclooctynone (BARAC); Rearrangement; Biomolecule Labelling; Applications; Bioconjugation; Imaging

…x28;2.1) are plotted against the various concentrations of the nitrone. All reactions were… …x28;2.1) plotted against the various concentrations of the nitrone. The slope represents… …against the various concentrations of the nitrone. The slope represents the second-order rate… …concentrations of the nitrone. The slope represents the second-order rate constant and equals to 41.0 M… …x28;2.1) plotted against the various concentrations of the nitrone. The slope represents… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chigrinova, M. (2014). Development of New Bioorthogonal Strain-Promoted Alkyne-Nitrone Cycloaddition Methodology for Applications in Living Systems . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/31281

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):

Chigrinova, Mariya. “Development of New Bioorthogonal Strain-Promoted Alkyne-Nitrone Cycloaddition Methodology for Applications in Living Systems .” 2014. Thesis, University of Ottawa. Accessed May 09, 2021. http://hdl.handle.net/10393/31281.

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

MLA Handbook (7th Edition):

Chigrinova, Mariya. “Development of New Bioorthogonal Strain-Promoted Alkyne-Nitrone Cycloaddition Methodology for Applications in Living Systems .” 2014. Web. 09 May 2021.

Vancouver:

Chigrinova M. Development of New Bioorthogonal Strain-Promoted Alkyne-Nitrone Cycloaddition Methodology for Applications in Living Systems . [Internet] [Thesis]. University of Ottawa; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/10393/31281.

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

Council of Science Editors:

Chigrinova M. Development of New Bioorthogonal Strain-Promoted Alkyne-Nitrone Cycloaddition Methodology for Applications in Living Systems . [Thesis]. University of Ottawa; 2014. Available from: http://hdl.handle.net/10393/31281

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

20. Richmond, Edward. An asymmetric pericyclic cascade approach to oxindoles.

Degree: 2014, University of St. Andrews

 The research in this thesis describes an asymmetric pericyclic cascade approach to the synthesis of a range of enantioenriched oxindoles using enantiopure oxazolidine derived nitrones… (more)

Subjects/Keywords: Pericyclic cascade; Cycloaddition; [3,3]; Nitrone; Ketene; Asymmetric; QD400.5S95R5; Heterocyclic compounds – Synthesis; Pericyclic reactions; Asymmetric synthesis

Page 1

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Richmond, E. (2014). An asymmetric pericyclic cascade approach to oxindoles. (Doctoral Dissertation). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/4459

Chicago Manual of Style (16th Edition):

Richmond, Edward. “An asymmetric pericyclic cascade approach to oxindoles.” 2014. Doctoral Dissertation, University of St. Andrews. Accessed May 09, 2021. http://hdl.handle.net/10023/4459.

MLA Handbook (7th Edition):

Richmond, Edward. “An asymmetric pericyclic cascade approach to oxindoles.” 2014. Web. 09 May 2021.

Vancouver:

Richmond E. An asymmetric pericyclic cascade approach to oxindoles. [Internet] [Doctoral dissertation]. University of St. Andrews; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/10023/4459.

Council of Science Editors:

Richmond E. An asymmetric pericyclic cascade approach to oxindoles. [Doctoral Dissertation]. University of St. Andrews; 2014. Available from: http://hdl.handle.net/10023/4459


ETH Zürich

21. Miescher, Karl. Nitrone und Nitrene.

Degree: 1918, ETH Zürich

Subjects/Keywords: NITRONE (ORGANISCHE CHEMIE); NITRENIUMIONEN + NITRENE (ORGANISCHE CHEMIE); NITRONES (ORGANIC CHEMISTRY); NITRENIUM IONS + NITRENES (ORGANIC CHEMISTRY); info:eu-repo/classification/ddc/540; Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Miescher, K. (1918). Nitrone und Nitrene. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/133041

Chicago Manual of Style (16th Edition):

Miescher, Karl. “Nitrone und Nitrene.” 1918. Doctoral Dissertation, ETH Zürich. Accessed May 09, 2021. http://hdl.handle.net/20.500.11850/133041.

MLA Handbook (7th Edition):

Miescher, Karl. “Nitrone und Nitrene.” 1918. Web. 09 May 2021.

Vancouver:

Miescher K. Nitrone und Nitrene. [Internet] [Doctoral dissertation]. ETH Zürich; 1918. [cited 2021 May 09]. Available from: http://hdl.handle.net/20.500.11850/133041.

Council of Science Editors:

Miescher K. Nitrone und Nitrene. [Doctoral Dissertation]. ETH Zürich; 1918. Available from: http://hdl.handle.net/20.500.11850/133041


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

22. Σταθάκης, Χρήστος. Σύνθεση κυκλιτολών και αμινοκυκλιτολών σε στερεή και υγρή φάση.

Degree: 2007, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

The present thesis is constituted of two main parts. The first part describes the synthesis of particular target-molecules, based on a methodology previously developed in… (more)

Subjects/Keywords: Κυκλοπροσθήκη νιτρόνης-ολεφίνης; Κυκλοπεντενόνες; Σύνθεση σε στερεά φάση; Νεπλανοσίνη Α; Πεντενομυκίνη Ι; Κυκλιτόλες; Αμινοκυκλιτόλες; Nitrone-olefin cycloaddition; Cyclopentenones; Solid phase synthesis; Neplanocin A; Pentenomycin I; Cyclitols; Aminocyclitols

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Σταθάκης, . . (2007). Σύνθεση κυκλιτολών και αμινοκυκλιτολών σε στερεή και υγρή φάση. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/19106

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):

Σταθάκης, Χρήστος. “Σύνθεση κυκλιτολών και αμινοκυκλιτολών σε στερεή και υγρή φάση.” 2007. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed May 09, 2021. http://hdl.handle.net/10442/hedi/19106.

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

MLA Handbook (7th Edition):

Σταθάκης, Χρήστος. “Σύνθεση κυκλιτολών και αμινοκυκλιτολών σε στερεή και υγρή φάση.” 2007. Web. 09 May 2021.

Vancouver:

Σταθάκης . Σύνθεση κυκλιτολών και αμινοκυκλιτολών σε στερεή και υγρή φάση. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2007. [cited 2021 May 09]. Available from: http://hdl.handle.net/10442/hedi/19106.

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

Council of Science Editors:

Σταθάκης . Σύνθεση κυκλιτολών και αμινοκυκλιτολών σε στερεή και υγρή φάση. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2007. Available from: http://hdl.handle.net/10442/hedi/19106

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

23. 須藤, 幸徳. 新規ルイス酸触媒(Nb,Yb)を用いる有用な触媒的炭素-炭素結合形成反応の開発 : Development of useful C・C bond formations using novel Lewis acid catalysts (Nb,Yb).

Degree: Chiba University / 千葉大学

研究科: 千葉大学大学院薬学研究院

修了年:2007

学位:千大院医薬博甲第薬54号

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

Subjects/Keywords: Lewis acid; niobium; ytterbium; Friedel-Crafts reaction; nitrone cycloaddition; Diels-Alder reaction; ルイス酸; ニオブ; イッテルビウム; Friedel-Crafts反応; ニトロン環化付加; Diels-Alder反応

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

須藤, . (n.d.). 新規ルイス酸触媒(Nb,Yb)を用いる有用な触媒的炭素-炭素結合形成反応の開発 : Development of useful C・C bond formations using novel Lewis acid catalysts (Nb,Yb). (Thesis). Chiba University / 千葉大学. Retrieved from http://opac.ll.chiba-u.jp/da/curator/900047202/

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

Chicago Manual of Style (16th Edition):

須藤, 幸徳. “新規ルイス酸触媒(Nb,Yb)を用いる有用な触媒的炭素-炭素結合形成反応の開発 : Development of useful C・C bond formations using novel Lewis acid catalysts (Nb,Yb).” Thesis, Chiba University / 千葉大学. Accessed May 09, 2021. http://opac.ll.chiba-u.jp/da/curator/900047202/.

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

MLA Handbook (7th Edition):

須藤, 幸徳. “新規ルイス酸触媒(Nb,Yb)を用いる有用な触媒的炭素-炭素結合形成反応の開発 : Development of useful C・C bond formations using novel Lewis acid catalysts (Nb,Yb).” Web. 09 May 2021.

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

Vancouver:

須藤 . 新規ルイス酸触媒(Nb,Yb)を用いる有用な触媒的炭素-炭素結合形成反応の開発 : Development of useful C・C bond formations using novel Lewis acid catalysts (Nb,Yb). [Internet] [Thesis]. Chiba University / 千葉大学; [cited 2021 May 09]. Available from: http://opac.ll.chiba-u.jp/da/curator/900047202/.

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

Council of Science Editors:

須藤 . 新規ルイス酸触媒(Nb,Yb)を用いる有用な触媒的炭素-炭素結合形成反応の開発 : Development of useful C・C bond formations using novel Lewis acid catalysts (Nb,Yb). [Thesis]. Chiba University / 千葉大学; Available from: http://opac.ll.chiba-u.jp/da/curator/900047202/

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


Queensland University of Technology

24. Micallef, Aaron Salvatore. Novel nitroxides and pronitroxides : synthesis and properties of new spin traps and spin probes with potential for biological application.

Degree: 2001, Queensland University of Technology

Subjects/Keywords: Nitroxides; Spin labels; nitroxide; nitroxyl; minoxyl; nitrone; isoindoline; spin trap; spin probe; spin label; radical; synthesis; EPR; ESR; partitioning; CHO cell; melanoma cell; chemistry; superoxide; nitric oxide; hydroxyl radical; thesis; doctoral

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Micallef, A. S. (2001). Novel nitroxides and pronitroxides : synthesis and properties of new spin traps and spin probes with potential for biological application. (Thesis). Queensland University of Technology. Retrieved from http://eprints.qut.edu.au/37085/

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):

Micallef, Aaron Salvatore. “Novel nitroxides and pronitroxides : synthesis and properties of new spin traps and spin probes with potential for biological application.” 2001. Thesis, Queensland University of Technology. Accessed May 09, 2021. http://eprints.qut.edu.au/37085/.

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

MLA Handbook (7th Edition):

Micallef, Aaron Salvatore. “Novel nitroxides and pronitroxides : synthesis and properties of new spin traps and spin probes with potential for biological application.” 2001. Web. 09 May 2021.

Vancouver:

Micallef AS. Novel nitroxides and pronitroxides : synthesis and properties of new spin traps and spin probes with potential for biological application. [Internet] [Thesis]. Queensland University of Technology; 2001. [cited 2021 May 09]. Available from: http://eprints.qut.edu.au/37085/.

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

Council of Science Editors:

Micallef AS. Novel nitroxides and pronitroxides : synthesis and properties of new spin traps and spin probes with potential for biological application. [Thesis]. Queensland University of Technology; 2001. Available from: http://eprints.qut.edu.au/37085/

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

25. Ghiassian, Sara. Strategies for Photochemical and Thermal Modification of Materials.

Degree: 2015, University of Western Ontario

 The modification of materials/surfaces is central to numerous applications ranging from opto-electronic devices to biomedical implants and drug delivery. Thus, there exists a high motivation… (more)

Subjects/Keywords: Surface modification; Gold nanoparticles; Photochemistry; Diazirine; Click-type reactions; Diels Alder; 1; 3-Dipolar cycloaddition; Strain-promoted alkyne-nitrone Cycloaddition; Materials Chemistry; Organic Chemistry

…Chapter 5: Nitrone Modified Gold Nanoparticles: Synthesis, Characterization and Their… …148 Figure 4.2. 1H NMR spectra in 5-9 ppm region for the reaction of compound 3 and nitrone… …1,3-dipolar cycloaddition reaction of Mal-EG4-AuNPs with nitrone D to yield B) 2DAuNP… …as a mixture of diastreomers and compound 3 with nitrone D to yield C) 4D-exo and D… …161 Figure 5.1. 1H NMR spectra of A) Me-EG3-AuNPs and B) Nitrone-AuNPs in D2O… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ghiassian, S. (2015). Strategies for Photochemical and Thermal Modification of Materials. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3009

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):

Ghiassian, Sara. “Strategies for Photochemical and Thermal Modification of Materials.” 2015. Thesis, University of Western Ontario. Accessed May 09, 2021. https://ir.lib.uwo.ca/etd/3009.

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

MLA Handbook (7th Edition):

Ghiassian, Sara. “Strategies for Photochemical and Thermal Modification of Materials.” 2015. Web. 09 May 2021.

Vancouver:

Ghiassian S. Strategies for Photochemical and Thermal Modification of Materials. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2021 May 09]. Available from: https://ir.lib.uwo.ca/etd/3009.

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

Council of Science Editors:

Ghiassian S. Strategies for Photochemical and Thermal Modification of Materials. [Thesis]. University of Western Ontario; 2015. Available from: https://ir.lib.uwo.ca/etd/3009

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


Queensland University of Technology

26. Smith, Craig David. Synthesis and properties of novel free radicals with potential as molecular magnetic materials and spin probes.

Degree: 2002, Queensland University of Technology

Subjects/Keywords: Free radicals (Chemistry); nitroxide; notroxyl; aminoxyl; isoindoline; nitronyl nitroxide; iminyl nitroxide; poperidinyl; nitrone; porphyrin; radical; biradical; triradical; synthesis; organic chemistry; EPR; ESR; exchange interaction; conformational exchange; ESI MS; magnetic susceptibility; molecular magnetic materials; fluorescence quenching; spin probes; thesis; doctoral

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Smith, C. D. (2002). Synthesis and properties of novel free radicals with potential as molecular magnetic materials and spin probes. (Thesis). Queensland University of Technology. Retrieved from http://eprints.qut.edu.au/37134/

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

Chicago Manual of Style (16th Edition):

Smith, Craig David. “Synthesis and properties of novel free radicals with potential as molecular magnetic materials and spin probes.” 2002. Thesis, Queensland University of Technology. Accessed May 09, 2021. http://eprints.qut.edu.au/37134/.

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

MLA Handbook (7th Edition):

Smith, Craig David. “Synthesis and properties of novel free radicals with potential as molecular magnetic materials and spin probes.” 2002. Web. 09 May 2021.

Vancouver:

Smith CD. Synthesis and properties of novel free radicals with potential as molecular magnetic materials and spin probes. [Internet] [Thesis]. Queensland University of Technology; 2002. [cited 2021 May 09]. Available from: http://eprints.qut.edu.au/37134/.

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

Council of Science Editors:

Smith CD. Synthesis and properties of novel free radicals with potential as molecular magnetic materials and spin probes. [Thesis]. Queensland University of Technology; 2002. Available from: http://eprints.qut.edu.au/37134/

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


ETH Zürich

27. Fässler, Roger. The metalation of terminal alkynes by Zn" and their addition to nitrones and aldehydes.

Degree: 2003, ETH Zürich

Subjects/Keywords: METALLIERUNG (CHEMISCHE REAKTIONEN); ALKINE (ORGANISCHE CHEMIE); ZINKORGANISCHE VERBINDUNGEN; ADDITIONSREAKTIONEN + KUPPLUNGSREAKTIONEN (CHEMISCHE REAKTIONEN); NITRONE (ORGANISCHE CHEMIE); ALDEHYDE (ORGANISCHE CHEMIE); METALATION (CHEMICAL REACTIONS); ALKYNES (ORGANIC CHEMISTRY); ZINC-ORGANIC COMPOUNDS; ADDITION REACTIONS + COUPLING REACTIONS (CHEMICAL REACTIONS); NITRONES (ORGANIC CHEMISTRY); ALDEHYDES (ORGANIC CHEMISTRY); info:eu-repo/classification/ddc/540; Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fässler, R. (2003). The metalation of terminal alkynes by Zn" and their addition to nitrones and aldehydes. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/147291

Chicago Manual of Style (16th Edition):

Fässler, Roger. “The metalation of terminal alkynes by Zn" and their addition to nitrones and aldehydes.” 2003. Doctoral Dissertation, ETH Zürich. Accessed May 09, 2021. http://hdl.handle.net/20.500.11850/147291.

MLA Handbook (7th Edition):

Fässler, Roger. “The metalation of terminal alkynes by Zn" and their addition to nitrones and aldehydes.” 2003. Web. 09 May 2021.

Vancouver:

Fässler R. The metalation of terminal alkynes by Zn" and their addition to nitrones and aldehydes. [Internet] [Doctoral dissertation]. ETH Zürich; 2003. [cited 2021 May 09]. Available from: http://hdl.handle.net/20.500.11850/147291.

Council of Science Editors:

Fässler R. The metalation of terminal alkynes by Zn" and their addition to nitrones and aldehydes. [Doctoral Dissertation]. ETH Zürich; 2003. Available from: http://hdl.handle.net/20.500.11850/147291

.