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You searched for subject:(Cyclopropene). Showing records 1 – 20 of 20 total matches.

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University of California – Irvine

1. Patterson, David Michael. New bioorthogonal chemistries for multi-component detection.

Degree: Chemistry, 2015, University of California – Irvine

 Bioorthogonal chemistries enable the selective visualization and identification of biomolecules in complex cellular environments. Significant advances in the speed and selectivity of these reactions have… (more)

Subjects/Keywords: Chemistry; bioorthogonal; cyclopropene

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APA (6th Edition):

Patterson, D. M. (2015). New bioorthogonal chemistries for multi-component detection. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/1vh6s9fz

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):

Patterson, David Michael. “New bioorthogonal chemistries for multi-component detection.” 2015. Thesis, University of California – Irvine. Accessed January 16, 2021. http://www.escholarship.org/uc/item/1vh6s9fz.

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

MLA Handbook (7th Edition):

Patterson, David Michael. “New bioorthogonal chemistries for multi-component detection.” 2015. Web. 16 Jan 2021.

Vancouver:

Patterson DM. New bioorthogonal chemistries for multi-component detection. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2021 Jan 16]. Available from: http://www.escholarship.org/uc/item/1vh6s9fz.

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

Council of Science Editors:

Patterson DM. New bioorthogonal chemistries for multi-component detection. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/1vh6s9fz

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


University of Tasmania

2. Howard, JK. New methods for the synthesis of nitrogen containing, biologically relevant small molecules.

Degree: 2015, University of Tasmania

 The following thesis consists of two independent parts, both linked by a common theme of developing new methods for the synthesis of small nitrogen containing… (more)

Subjects/Keywords: Pyrrole; Cyclopropene; Oxidation; Rearrangement; Pyrrolinone; Photochemistry

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APA (6th Edition):

Howard, J. (2015). New methods for the synthesis of nitrogen containing, biologically relevant small molecules. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/22887/1/Howard_whole_thesis.pdf

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

Chicago Manual of Style (16th Edition):

Howard, JK. “New methods for the synthesis of nitrogen containing, biologically relevant small molecules.” 2015. Thesis, University of Tasmania. Accessed January 16, 2021. https://eprints.utas.edu.au/22887/1/Howard_whole_thesis.pdf.

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

MLA Handbook (7th Edition):

Howard, JK. “New methods for the synthesis of nitrogen containing, biologically relevant small molecules.” 2015. Web. 16 Jan 2021.

Vancouver:

Howard J. New methods for the synthesis of nitrogen containing, biologically relevant small molecules. [Internet] [Thesis]. University of Tasmania; 2015. [cited 2021 Jan 16]. Available from: https://eprints.utas.edu.au/22887/1/Howard_whole_thesis.pdf.

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

Council of Science Editors:

Howard J. New methods for the synthesis of nitrogen containing, biologically relevant small molecules. [Thesis]. University of Tasmania; 2015. Available from: https://eprints.utas.edu.au/22887/1/Howard_whole_thesis.pdf

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


NSYSU

3. Hsueh, Yu-Tan. 1.Pyrolytic Studies of Arylimines 2.Synthetic Studies of Natural Products With 2-Phenylbenzofuran framework by the Flash Vacuum Pyrolysis 3.Pyrolytic Studies of Furylmethyl benzoatesãBenzothienylmethyl benzoates and N-Methylpyrrolylmethyl benzoates.

Degree: PhD, Chemistry, 2011, NSYSU

 The thesis is divided into three chapters Chapter 1ãFlash vacuum pyrolysis of 2-chloro-N-arenylideneaniline gave quinolines by the intromolecular cyclization. And then, flash vacuum pyrolysis of… (more)

Subjects/Keywords: flash vacuum pyrolysis; benzothi-azoles; vinylcarbene-cyclopropene; N-arenylideneanilines; 2-phenylbenzofuran

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APA (6th Edition):

Hsueh, Y. (2011). 1.Pyrolytic Studies of Arylimines 2.Synthetic Studies of Natural Products With 2-Phenylbenzofuran framework by the Flash Vacuum Pyrolysis 3.Pyrolytic Studies of Furylmethyl benzoatesãBenzothienylmethyl benzoates and N-Methylpyrrolylmethyl benzoates. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907111-145302

Chicago Manual of Style (16th Edition):

Hsueh, Yu-Tan. “1.Pyrolytic Studies of Arylimines 2.Synthetic Studies of Natural Products With 2-Phenylbenzofuran framework by the Flash Vacuum Pyrolysis 3.Pyrolytic Studies of Furylmethyl benzoatesãBenzothienylmethyl benzoates and N-Methylpyrrolylmethyl benzoates.” 2011. Doctoral Dissertation, NSYSU. Accessed January 16, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907111-145302.

MLA Handbook (7th Edition):

Hsueh, Yu-Tan. “1.Pyrolytic Studies of Arylimines 2.Synthetic Studies of Natural Products With 2-Phenylbenzofuran framework by the Flash Vacuum Pyrolysis 3.Pyrolytic Studies of Furylmethyl benzoatesãBenzothienylmethyl benzoates and N-Methylpyrrolylmethyl benzoates.” 2011. Web. 16 Jan 2021.

Vancouver:

Hsueh Y. 1.Pyrolytic Studies of Arylimines 2.Synthetic Studies of Natural Products With 2-Phenylbenzofuran framework by the Flash Vacuum Pyrolysis 3.Pyrolytic Studies of Furylmethyl benzoatesãBenzothienylmethyl benzoates and N-Methylpyrrolylmethyl benzoates. [Internet] [Doctoral dissertation]. NSYSU; 2011. [cited 2021 Jan 16]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907111-145302.

Council of Science Editors:

Hsueh Y. 1.Pyrolytic Studies of Arylimines 2.Synthetic Studies of Natural Products With 2-Phenylbenzofuran framework by the Flash Vacuum Pyrolysis 3.Pyrolytic Studies of Furylmethyl benzoatesãBenzothienylmethyl benzoates and N-Methylpyrrolylmethyl benzoates. [Doctoral Dissertation]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0907111-145302


University of Kansas

4. Alnasleh, Bassam Kamal. Development of Methods for the Heteroatom Functionalization of Cyclopropenes.

Degree: PhD, Chemistry, 2011, University of Kansas

 The main focus of this thesis is the stereoselective funtionalization of cyclopropenes mainly via the addition of H-X (hetroatom-hydrogen) moieties across the strained double bond.… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Cyclization; Cyclopropane; Cyclopropene; Hydrophosphination; Hydrophosphorylation; Substitution

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APA (6th Edition):

Alnasleh, B. K. (2011). Development of Methods for the Heteroatom Functionalization of Cyclopropenes. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/10704

Chicago Manual of Style (16th Edition):

Alnasleh, Bassam Kamal. “Development of Methods for the Heteroatom Functionalization of Cyclopropenes.” 2011. Doctoral Dissertation, University of Kansas. Accessed January 16, 2021. http://hdl.handle.net/1808/10704.

MLA Handbook (7th Edition):

Alnasleh, Bassam Kamal. “Development of Methods for the Heteroatom Functionalization of Cyclopropenes.” 2011. Web. 16 Jan 2021.

Vancouver:

Alnasleh BK. Development of Methods for the Heteroatom Functionalization of Cyclopropenes. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1808/10704.

Council of Science Editors:

Alnasleh BK. Development of Methods for the Heteroatom Functionalization of Cyclopropenes. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/10704


Loughborough University

5. Watson, Hayley. Synthesis and reactivity of cyclopropanes and cyclopropenes.

Degree: PhD, 2011, Loughborough University

 Activated cyclopropanes have been extensively used in synthetic chemistry as precursors for cycloaddition reactions. The rationale behind this is their ability to undergo ring-opening when… (more)

Subjects/Keywords: 547.6; Cycloaddition; Cyclopropane; Cyclopropene; Nucleophilic addition; Oxazine; Ring-opening

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APA (6th Edition):

Watson, H. (2011). Synthesis and reactivity of cyclopropanes and cyclopropenes. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/9032

Chicago Manual of Style (16th Edition):

Watson, Hayley. “Synthesis and reactivity of cyclopropanes and cyclopropenes.” 2011. Doctoral Dissertation, Loughborough University. Accessed January 16, 2021. http://hdl.handle.net/2134/9032.

MLA Handbook (7th Edition):

Watson, Hayley. “Synthesis and reactivity of cyclopropanes and cyclopropenes.” 2011. Web. 16 Jan 2021.

Vancouver:

Watson H. Synthesis and reactivity of cyclopropanes and cyclopropenes. [Internet] [Doctoral dissertation]. Loughborough University; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/2134/9032.

Council of Science Editors:

Watson H. Synthesis and reactivity of cyclopropanes and cyclopropenes. [Doctoral Dissertation]. Loughborough University; 2011. Available from: http://hdl.handle.net/2134/9032

6. Phan, Diem. Enantioselective Rhodium-catalyzed Hydroacylation of Alkenes and Ketones & Silver-catalyzed Hydroamination of Cyclopropenes.

Degree: 2012, University of Toronto

Due to the scarcity of energy resources that we are facing today, there is an increasing need for new methodology developments that are green and… (more)

Subjects/Keywords: hydroacylation; cyclopropene; 0490

…Evaluating Different Catalysts for Hydroamination of Cyclopropene 4.43 .............. 271 Table… …4.2 Hydroamination of Cyclopropene 4.43 with Different Amines… …273 Table ‎ 4.3 Hydroamination of Cyclopropene 4.44 with Different Amines… …177 Scheme ‎ 4.1 Padwa’s Proposed Mechanism for Ag-Promoted Isomerization of Cyclopropene… …188 Figure ‎ 4.1 Selected Examples of Cyclopropene Ring-Cleavage Chemistry… 

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APA (6th Edition):

Phan, D. (2012). Enantioselective Rhodium-catalyzed Hydroacylation of Alkenes and Ketones & Silver-catalyzed Hydroamination of Cyclopropenes. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32865

Chicago Manual of Style (16th Edition):

Phan, Diem. “Enantioselective Rhodium-catalyzed Hydroacylation of Alkenes and Ketones & Silver-catalyzed Hydroamination of Cyclopropenes.” 2012. Doctoral Dissertation, University of Toronto. Accessed January 16, 2021. http://hdl.handle.net/1807/32865.

MLA Handbook (7th Edition):

Phan, Diem. “Enantioselective Rhodium-catalyzed Hydroacylation of Alkenes and Ketones & Silver-catalyzed Hydroamination of Cyclopropenes.” 2012. Web. 16 Jan 2021.

Vancouver:

Phan D. Enantioselective Rhodium-catalyzed Hydroacylation of Alkenes and Ketones & Silver-catalyzed Hydroamination of Cyclopropenes. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1807/32865.

Council of Science Editors:

Phan D. Enantioselective Rhodium-catalyzed Hydroacylation of Alkenes and Ketones & Silver-catalyzed Hydroamination of Cyclopropenes. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32865

7. Banning, Joseph Erik. Strain-Release Activation of α,β-Unsaturated Amides Towards Conjugate Addition of N, O and S - Nucleophiles.

Degree: PhD, Chemistry, 2013, University of Kansas

 This thesis encompasses a novel methodology enabling the diastereoselective addition of heteroatom-centered nucleophiles to the conjugated double bond of in situ-generated α,β - unsaturated cyclopropenyl… (more)

Subjects/Keywords: Organic chemistry; Cyclopropane; Cyclopropene

cyclopropene is accompanied by large amounts of strain energy because of the fact that it contains… …instability but also that cyclopropene can serve as an effective energy reserve for driving… …enables the direct functionalization of cyclopropene with a variety of donor groups, or… …trapping of cyclopropene with alkoxide nucleophiles Rubin and coworkers has demonstrated that… …while cyclopropene 65 can be synthesized, isolated and stored under nitrogen at low… 

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APA (6th Edition):

Banning, J. E. (2013). Strain-Release Activation of α,β-Unsaturated Amides Towards Conjugate Addition of N, O and S - Nucleophiles. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/12303

Chicago Manual of Style (16th Edition):

Banning, Joseph Erik. “Strain-Release Activation of α,β-Unsaturated Amides Towards Conjugate Addition of N, O and S - Nucleophiles.” 2013. Doctoral Dissertation, University of Kansas. Accessed January 16, 2021. http://hdl.handle.net/1808/12303.

MLA Handbook (7th Edition):

Banning, Joseph Erik. “Strain-Release Activation of α,β-Unsaturated Amides Towards Conjugate Addition of N, O and S - Nucleophiles.” 2013. Web. 16 Jan 2021.

Vancouver:

Banning JE. Strain-Release Activation of α,β-Unsaturated Amides Towards Conjugate Addition of N, O and S - Nucleophiles. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1808/12303.

Council of Science Editors:

Banning JE. Strain-Release Activation of α,β-Unsaturated Amides Towards Conjugate Addition of N, O and S - Nucleophiles. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/12303


University of Kansas

8. Edwards, Andrew. Stereoselective Additions to Cyclopropenes.

Degree: PhD, Chemistry, 2018, University of Kansas

 This thesis concerns strain-release driven stereoselective addition reactions to cyclopropenes leading to the synthesis of medium-sized 8-membered 1,5-dioxocane ring structures, optically active cyclopropylboronates, and densely… (more)

Subjects/Keywords: Organic chemistry; Carbomagnesiation; Catalytic; Cyclopropene; Directed; Hydroboration; Stereoselective

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APA (6th Edition):

Edwards, A. (2018). Stereoselective Additions to Cyclopropenes. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/27877

Chicago Manual of Style (16th Edition):

Edwards, Andrew. “Stereoselective Additions to Cyclopropenes.” 2018. Doctoral Dissertation, University of Kansas. Accessed January 16, 2021. http://hdl.handle.net/1808/27877.

MLA Handbook (7th Edition):

Edwards, Andrew. “Stereoselective Additions to Cyclopropenes.” 2018. Web. 16 Jan 2021.

Vancouver:

Edwards A. Stereoselective Additions to Cyclopropenes. [Internet] [Doctoral dissertation]. University of Kansas; 2018. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1808/27877.

Council of Science Editors:

Edwards A. Stereoselective Additions to Cyclopropenes. [Doctoral Dissertation]. University of Kansas; 2018. Available from: http://hdl.handle.net/1808/27877


University of California – Irvine

9. Nazarova, Lidia. Development of bioorthogonal chemical reporters for studying host-pathogen interactions.

Degree: Chemistry, 2015, University of California – Irvine

 Bioorthogonal chemical reporters are small functional groups that can be metabolically incorporated into biomolecules by the cell’s native metabolic machinery. These moieties can be covalently… (more)

Subjects/Keywords: Chemistry; Biochemistry; Molecular biology; Bioorthogonal reaction; Chemical reporter; Cycloaddition; Cyclopropene; Glycosylation; Toxoplasma

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APA (6th Edition):

Nazarova, L. (2015). Development of bioorthogonal chemical reporters for studying host-pathogen interactions. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/0kd202wk

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):

Nazarova, Lidia. “Development of bioorthogonal chemical reporters for studying host-pathogen interactions.” 2015. Thesis, University of California – Irvine. Accessed January 16, 2021. http://www.escholarship.org/uc/item/0kd202wk.

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

MLA Handbook (7th Edition):

Nazarova, Lidia. “Development of bioorthogonal chemical reporters for studying host-pathogen interactions.” 2015. Web. 16 Jan 2021.

Vancouver:

Nazarova L. Development of bioorthogonal chemical reporters for studying host-pathogen interactions. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2021 Jan 16]. Available from: http://www.escholarship.org/uc/item/0kd202wk.

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

Council of Science Editors:

Nazarova L. Development of bioorthogonal chemical reporters for studying host-pathogen interactions. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/0kd202wk

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


University of Delaware

10. LI, YI. Stereoselective synthesis of butenolides and its applications in total synthesis of sessilifoliamides and development of new chemical tools for hydrogel based biomaterials.

Degree: PhD, University of Delaware, Department of Chemistry and Biochemistry, 2017, University of Delaware

 The research in my doctoral study consists of two major parts. One part is a synthetic method development and its applications in solving complex synthetic… (more)

Subjects/Keywords: Pure sciences; Applied sciences; 3D cell culture; Bioorthogonal reaction; Butenolides; Cyclopropene; Sessilifoliamides

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APA (6th Edition):

LI, Y. (2017). Stereoselective synthesis of butenolides and its applications in total synthesis of sessilifoliamides and development of new chemical tools for hydrogel based biomaterials. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/21741

Chicago Manual of Style (16th Edition):

LI, YI. “Stereoselective synthesis of butenolides and its applications in total synthesis of sessilifoliamides and development of new chemical tools for hydrogel based biomaterials.” 2017. Doctoral Dissertation, University of Delaware. Accessed January 16, 2021. http://udspace.udel.edu/handle/19716/21741.

MLA Handbook (7th Edition):

LI, YI. “Stereoselective synthesis of butenolides and its applications in total synthesis of sessilifoliamides and development of new chemical tools for hydrogel based biomaterials.” 2017. Web. 16 Jan 2021.

Vancouver:

LI Y. Stereoselective synthesis of butenolides and its applications in total synthesis of sessilifoliamides and development of new chemical tools for hydrogel based biomaterials. [Internet] [Doctoral dissertation]. University of Delaware; 2017. [cited 2021 Jan 16]. Available from: http://udspace.udel.edu/handle/19716/21741.

Council of Science Editors:

LI Y. Stereoselective synthesis of butenolides and its applications in total synthesis of sessilifoliamides and development of new chemical tools for hydrogel based biomaterials. [Doctoral Dissertation]. University of Delaware; 2017. Available from: http://udspace.udel.edu/handle/19716/21741

11. Wang, Yi. Stereoselective synthesis of multisubstituted alkenes via ring opening reactions of cyclopropenes : enantioselective copper catalysed asymmetric reduction of alkenylheteroarenes.

Degree: PhD, 2010, University of Edinburgh

 A catalytic organometallic addition-ring opening sequence of cyclopropenes that enables the efficient and highly stereoselective synthesis of multisubstituted alkenes has been developed. A possible mechanism… (more)

Subjects/Keywords: 547.4; alkene; cyclopropene; copper; reduction

…TMS trimethylsilyl i Table of Contents 1) Cyclopropene Chemistry: An Overview… …olefins using transition metal catalyst, one is cyclopropene addition-ring opening reaction, and… …novel cyclopropene chemistry have been carried out. Dr Euan Fordyce developed two new… …I finished cyclopropene chemistry projects, I joined them and tried to synthesise other… …tolerate more challenging heteroarene substrates. 1 1) Cyclopropene Chemistry: An… 

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APA (6th Edition):

Wang, Y. (2010). Stereoselective synthesis of multisubstituted alkenes via ring opening reactions of cyclopropenes : enantioselective copper catalysed asymmetric reduction of alkenylheteroarenes. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4607

Chicago Manual of Style (16th Edition):

Wang, Yi. “Stereoselective synthesis of multisubstituted alkenes via ring opening reactions of cyclopropenes : enantioselective copper catalysed asymmetric reduction of alkenylheteroarenes.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed January 16, 2021. http://hdl.handle.net/1842/4607.

MLA Handbook (7th Edition):

Wang, Yi. “Stereoselective synthesis of multisubstituted alkenes via ring opening reactions of cyclopropenes : enantioselective copper catalysed asymmetric reduction of alkenylheteroarenes.” 2010. Web. 16 Jan 2021.

Vancouver:

Wang Y. Stereoselective synthesis of multisubstituted alkenes via ring opening reactions of cyclopropenes : enantioselective copper catalysed asymmetric reduction of alkenylheteroarenes. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1842/4607.

Council of Science Editors:

Wang Y. Stereoselective synthesis of multisubstituted alkenes via ring opening reactions of cyclopropenes : enantioselective copper catalysed asymmetric reduction of alkenylheteroarenes. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4607


University of Kansas

12. Ryabchuk, Pavel. Synthesis of Densely Functionalized Cyclopropanes via Diastereoselective Nucleophilic Additions to in Situ Generated Cyclopropenes.

Degree: PhD, Chemistry, 2013, University of Kansas

 This thesis is concerned with the development and application of methods for the diastereoselective synthesis of substituted cyclopropanes. The methodology described in this dissertation is… (more)

Subjects/Keywords: Chemistry; Aminocyclopropanecarboxylic acid; Aza-michael; Bromocyclopropanes; Cyclopropene; Donor-acceptor cyclopropanes; Oxa-michael

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APA (6th Edition):

Ryabchuk, P. (2013). Synthesis of Densely Functionalized Cyclopropanes via Diastereoselective Nucleophilic Additions to in Situ Generated Cyclopropenes. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/14829

Chicago Manual of Style (16th Edition):

Ryabchuk, Pavel. “Synthesis of Densely Functionalized Cyclopropanes via Diastereoselective Nucleophilic Additions to in Situ Generated Cyclopropenes.” 2013. Doctoral Dissertation, University of Kansas. Accessed January 16, 2021. http://hdl.handle.net/1808/14829.

MLA Handbook (7th Edition):

Ryabchuk, Pavel. “Synthesis of Densely Functionalized Cyclopropanes via Diastereoselective Nucleophilic Additions to in Situ Generated Cyclopropenes.” 2013. Web. 16 Jan 2021.

Vancouver:

Ryabchuk P. Synthesis of Densely Functionalized Cyclopropanes via Diastereoselective Nucleophilic Additions to in Situ Generated Cyclopropenes. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1808/14829.

Council of Science Editors:

Ryabchuk P. Synthesis of Densely Functionalized Cyclopropanes via Diastereoselective Nucleophilic Additions to in Situ Generated Cyclopropenes. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/14829


University of Illinois – Chicago

13. Li, Jingwei. Tandem Metathesis-Based Natural Product Synthesis & Synthesis of Cyclopropenes and Their Rearrangements.

Degree: 2013, University of Illinois – Chicago

 This thesis contains two parts. Part I is about the development and application of tandem metathesis reactions to the synthesis of natural products, which is… (more)

Subjects/Keywords: Tandem Enyne Metathesis; Ring-Rearrangement Metathesis; Natural Product Synthesis; Epoxyquinoids; Galanthamine; Caribenol A; Cyclopropene; Alkylidene Carbene; Allene

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APA (6th Edition):

Li, J. (2013). Tandem Metathesis-Based Natural Product Synthesis & Synthesis of Cyclopropenes and Their Rearrangements. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10055

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):

Li, Jingwei. “Tandem Metathesis-Based Natural Product Synthesis & Synthesis of Cyclopropenes and Their Rearrangements.” 2013. Thesis, University of Illinois – Chicago. Accessed January 16, 2021. http://hdl.handle.net/10027/10055.

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

MLA Handbook (7th Edition):

Li, Jingwei. “Tandem Metathesis-Based Natural Product Synthesis & Synthesis of Cyclopropenes and Their Rearrangements.” 2013. Web. 16 Jan 2021.

Vancouver:

Li J. Tandem Metathesis-Based Natural Product Synthesis & Synthesis of Cyclopropenes and Their Rearrangements. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10027/10055.

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

Council of Science Editors:

Li J. Tandem Metathesis-Based Natural Product Synthesis & Synthesis of Cyclopropenes and Their Rearrangements. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10055

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


University of Illinois – Chicago

14. Sun, Chunrui. New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions.

Degree: 2013, University of Illinois – Chicago

 This thesis contains two parts. Part I is about the development of novel α-amination of carbonyl compounds using lithium trimethylsilyldiazomethane and its application to the… (more)

Subjects/Keywords: lithium trimethylsilyldiazomethane; [3+2] cycloaddition; N–N bond cleavage; α-amination; amathaspiramide; massadine; cyclopropene; C–H amination

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APA (6th Edition):

Sun, C. (2013). New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10062

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):

Sun, Chunrui. “New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions.” 2013. Thesis, University of Illinois – Chicago. Accessed January 16, 2021. http://hdl.handle.net/10027/10062.

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

MLA Handbook (7th Edition):

Sun, Chunrui. “New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions.” 2013. Web. 16 Jan 2021.

Vancouver:

Sun C. New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10027/10062.

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

Council of Science Editors:

Sun C. New Chemistry of Lithium Trimethylsilyldiazomethane & Development of Novel Amination Reactions. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10062

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


University of Kansas

15. Sherrill, William M. Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles.

Degree: PhD, Chemistry, 2009, University of Kansas

 This document deals with 3-membered carbocycles; their use as ligands for the asymmetric Heck reaction (AHR), the development of novel methods for their synthesis, and… (more)

Subjects/Keywords: Organic chemistry; Asymmetric; Carbocycles; Cyclopropene; Heck reaction; Hydroformylation; Synthesis

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APA (6th Edition):

Sherrill, W. M. (2009). Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/5260

Chicago Manual of Style (16th Edition):

Sherrill, William M. “Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles.” 2009. Doctoral Dissertation, University of Kansas. Accessed January 16, 2021. http://hdl.handle.net/1808/5260.

MLA Handbook (7th Edition):

Sherrill, William M. “Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles.” 2009. Web. 16 Jan 2021.

Vancouver:

Sherrill WM. Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles. [Internet] [Doctoral dissertation]. University of Kansas; 2009. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1808/5260.

Council of Science Editors:

Sherrill WM. Development of Novel Transition Metal Catalyzed Transformations Involving Small, Strained Carbocycles. [Doctoral Dissertation]. University of Kansas; 2009. Available from: http://hdl.handle.net/1808/5260

16. Phun, Lien Hoang. Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles.

Degree: PhD, Chemistry and Biochemistry, 2013, Georgia Tech

 Natural products and small molecules play a major role in drug development. However, using natural products as a source of medicine comes with many challenges,… (more)

Subjects/Keywords: Furans; Carbocycles; Heterocycles; Cyclopropane; Cyclopropene; Diazo; Drug development; Pharmacognosy

…Table 4.2: Heteroaryl Cyclopropene Synthesis 128 Table 4.3: Cycloisomerization of 3,3… …Seven-membered Rings 8 Figure 1.6: Walsh Model of Cyclopropene 18 Figure 1.7: Resonance… …1.19: Dem’yanov and Doyarenko’s Synthesis of Cyclopropene 19 Scheme 1.20: Ring-Opening… …Isomerization of Cyclopropene 121 Scheme 4.5: Shi’s Lewis Acid Catalyzed Cycloisomerization of… …Proposed Mechanism for Indene Formation 122 Scheme 4.8: Synthesis of Model Cyclopropene… 

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APA (6th Edition):

Phun, L. H. (2013). Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/47542

Chicago Manual of Style (16th Edition):

Phun, Lien Hoang. “Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles.” 2013. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/47542.

MLA Handbook (7th Edition):

Phun, Lien Hoang. “Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles.” 2013. Web. 16 Jan 2021.

Vancouver:

Phun LH. Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/47542.

Council of Science Editors:

Phun LH. Innovative approaches to carbocyclic and heterocyclic compounds using strained carbocycles. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/47542

17. Matheny, Jonathon Paul. Synthesis of Cyclopropane-Fused 1,5-Diazocin-2-ones via Metal-Templated Intramolecular Addition of Nitrogen Nucleophiles to Pre-Generated Cyclopropenes.

Degree: MS, Chemistry, 2018, University of Kansas

 This thesis is concerned with the development of methods by which to access compounds possessing the 3,4-cyclopropane-annulated 1,5-diazocin-2-one scaffold. The methods described herein are based… (more)

Subjects/Keywords: Organic chemistry; azalactam; cyclization; cyclopropane; cyclopropene; diazocinone; medium-sized heterocycle

…66 2.9.3. Synthesis of Cyclopropene Carboxamides… 

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APA (6th Edition):

Matheny, J. P. (2018). Synthesis of Cyclopropane-Fused 1,5-Diazocin-2-ones via Metal-Templated Intramolecular Addition of Nitrogen Nucleophiles to Pre-Generated Cyclopropenes. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/27827

Chicago Manual of Style (16th Edition):

Matheny, Jonathon Paul. “Synthesis of Cyclopropane-Fused 1,5-Diazocin-2-ones via Metal-Templated Intramolecular Addition of Nitrogen Nucleophiles to Pre-Generated Cyclopropenes.” 2018. Masters Thesis, University of Kansas. Accessed January 16, 2021. http://hdl.handle.net/1808/27827.

MLA Handbook (7th Edition):

Matheny, Jonathon Paul. “Synthesis of Cyclopropane-Fused 1,5-Diazocin-2-ones via Metal-Templated Intramolecular Addition of Nitrogen Nucleophiles to Pre-Generated Cyclopropenes.” 2018. Web. 16 Jan 2021.

Vancouver:

Matheny JP. Synthesis of Cyclopropane-Fused 1,5-Diazocin-2-ones via Metal-Templated Intramolecular Addition of Nitrogen Nucleophiles to Pre-Generated Cyclopropenes. [Internet] [Masters thesis]. University of Kansas; 2018. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1808/27827.

Council of Science Editors:

Matheny JP. Synthesis of Cyclopropane-Fused 1,5-Diazocin-2-ones via Metal-Templated Intramolecular Addition of Nitrogen Nucleophiles to Pre-Generated Cyclopropenes. [Masters Thesis]. University of Kansas; 2018. Available from: http://hdl.handle.net/1808/27827


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

18. Γιαννούσης, Κωνσταντίνος. Επίδραση των 1-MCP, σαλικυλικού οξέος και υπεροξειδίου του υδρογόνου στην ποιότητα και συντηρησιμότητα των καρπών ποικιλιών μηλιάς (Malus pumila M...

Degree: 2012, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

Apples contain a variety of antioxidant substances with beneficial activity for human health and they are highly ranked for their contribution in per capita consumption… (more)

Subjects/Keywords: Μήλα; Αντιοξειδωτικά; Συντήρηση; Ποιότητα; Σαλικυλικό οξύ; Υπεροξείδιο του υδρογόνου; 1-μεθυλοκυκλοπροπένιο (1-MCP); Φαινόλες; Apples; Antioxidants; Storage; Quality; Salicylic acid (SA); Hydrogen peroxide; 1-methyl cyclopropene (1-MCP); Phenolics

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APA (6th Edition):

Γιαννούσης, . . (2012). Επίδραση των 1-MCP, σαλικυλικού οξέος και υπεροξειδίου του υδρογόνου στην ποιότητα και συντηρησιμότητα των καρπών ποικιλιών μηλιάς (Malus pumila M... (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/26953

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):

Γιαννούσης, Κωνσταντίνος. “Επίδραση των 1-MCP, σαλικυλικού οξέος και υπεροξειδίου του υδρογόνου στην ποιότητα και συντηρησιμότητα των καρπών ποικιλιών μηλιάς (Malus pumila M...” 2012. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed January 16, 2021. http://hdl.handle.net/10442/hedi/26953.

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

MLA Handbook (7th Edition):

Γιαννούσης, Κωνσταντίνος. “Επίδραση των 1-MCP, σαλικυλικού οξέος και υπεροξειδίου του υδρογόνου στην ποιότητα και συντηρησιμότητα των καρπών ποικιλιών μηλιάς (Malus pumila M...” 2012. Web. 16 Jan 2021.

Vancouver:

Γιαννούσης . Επίδραση των 1-MCP, σαλικυλικού οξέος και υπεροξειδίου του υδρογόνου στην ποιότητα και συντηρησιμότητα των καρπών ποικιλιών μηλιάς (Malus pumila M... [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2012. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10442/hedi/26953.

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

Council of Science Editors:

Γιαννούσης . Επίδραση των 1-MCP, σαλικυλικού οξέος και υπεροξειδίου του υδρογόνου στην ποιότητα και συντηρησιμότητα των καρπών ποικιλιών μηλιάς (Malus pumila M... [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2012. Available from: http://hdl.handle.net/10442/hedi/26953

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


ETH Zürich

19. Vasilatou, Konstantina. High-resolution photoelectron spectroscopy.

Degree: 2013, ETH Zürich

Subjects/Keywords: XENON (CHEMISCHE ELEMENTE); CYCLOPROPENE AND DERIVATIVES (ALICYCLIC HYDROCARBONS); CATIONS (CHEMISTRY); MOLECULAR IONS (CHEMISTRY); PHOTOELECTRON SPECTROSCOPY (PARTICLE PHYSICS); CYCLOPROPEN UND DERIVATE (ALICYCLISCHE KOHLENWASSERSTOFFE); PROPEN UND DERIVATE (ALIPHATISCHE UNGESÄTTIGTE KOHLENWASSERSTOFFE); PROPYLENE AND DERIVATIVES (ALIPHATIC UNSATURATED HYDROCARBONS); XENON (CHEMICAL ELEMENTS); PHOTOELEKTRONENSPEKTROSKOPIE (TEILCHENPHYSIK); KATIONEN (CHEMIE); MOLEKÜLIONEN (CHEMIE); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Vasilatou, K. (2013). High-resolution photoelectron spectroscopy. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/79553

Chicago Manual of Style (16th Edition):

Vasilatou, Konstantina. “High-resolution photoelectron spectroscopy.” 2013. Doctoral Dissertation, ETH Zürich. Accessed January 16, 2021. http://hdl.handle.net/20.500.11850/79553.

MLA Handbook (7th Edition):

Vasilatou, Konstantina. “High-resolution photoelectron spectroscopy.” 2013. Web. 16 Jan 2021.

Vancouver:

Vasilatou K. High-resolution photoelectron spectroscopy. [Internet] [Doctoral dissertation]. ETH Zürich; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/20.500.11850/79553.

Council of Science Editors:

Vasilatou K. High-resolution photoelectron spectroscopy. [Doctoral Dissertation]. ETH Zürich; 2013. Available from: http://hdl.handle.net/20.500.11850/79553


ETH Zürich

20. Haerdi, Wilhelm. Der Einfluss der Phenylgruppe auf die Bildung des Cyclopropan- und des Cyclopropenringes.

Degree: 1925, ETH Zürich

Subjects/Keywords: CYCLOPROPAN UND DERIVATE (ALICYCLISCHE KOHLENWASSERSTOFFE); CYCLOPROPEN UND DERIVATE (ALICYCLISCHE KOHLENWASSERSTOFFE); ORGANISCHE SYNTHESE (CHEMIE); REAKTIONSMECHANISMEN + REAKTIVITÄT (CHEMISCHE KINETIK); CYCLOPROPANE AND DERIVATIVES (ALICYCLIC HYDROCARBONS); CYCLOPROPENE AND DERIVATIVES (ALICYCLIC HYDROCARBONS); ORGANIC SYNTHESIS (CHEMISTRY); REACTION MECHANISMS + REACTIVITY (CHEMICAL KINETICS); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Haerdi, W. (1925). Der Einfluss der Phenylgruppe auf die Bildung des Cyclopropan- und des Cyclopropenringes. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/135255

Chicago Manual of Style (16th Edition):

Haerdi, Wilhelm. “Der Einfluss der Phenylgruppe auf die Bildung des Cyclopropan- und des Cyclopropenringes.” 1925. Doctoral Dissertation, ETH Zürich. Accessed January 16, 2021. http://hdl.handle.net/20.500.11850/135255.

MLA Handbook (7th Edition):

Haerdi, Wilhelm. “Der Einfluss der Phenylgruppe auf die Bildung des Cyclopropan- und des Cyclopropenringes.” 1925. Web. 16 Jan 2021.

Vancouver:

Haerdi W. Der Einfluss der Phenylgruppe auf die Bildung des Cyclopropan- und des Cyclopropenringes. [Internet] [Doctoral dissertation]. ETH Zürich; 1925. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/20.500.11850/135255.

Council of Science Editors:

Haerdi W. Der Einfluss der Phenylgruppe auf die Bildung des Cyclopropan- und des Cyclopropenringes. [Doctoral Dissertation]. ETH Zürich; 1925. Available from: http://hdl.handle.net/20.500.11850/135255

.