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You searched for subject:(allenes). Showing records 1 – 30 of 45 total matches.

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University of Georgia

1. Bui, Binh H. Thermal rearrangements of heteroatom-bridged polyunsaturated hydrocarbons.

Degree: MS, Chemistry, 2006, University of Georgia

 In predicting new reactions, systematic strategies involving the classification of systems of interest and methodological applications of computational tools are used to study heterosubstituted polyunsaturated… (more)

Subjects/Keywords: enyne-allenes

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

APA (6th Edition):

Bui, B. H. (2006). Thermal rearrangements of heteroatom-bridged polyunsaturated hydrocarbons. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/bui_binh_h_200608_ms

Chicago Manual of Style (16th Edition):

Bui, Binh H. “Thermal rearrangements of heteroatom-bridged polyunsaturated hydrocarbons.” 2006. Masters Thesis, University of Georgia. Accessed October 16, 2019. http://purl.galileo.usg.edu/uga_etd/bui_binh_h_200608_ms.

MLA Handbook (7th Edition):

Bui, Binh H. “Thermal rearrangements of heteroatom-bridged polyunsaturated hydrocarbons.” 2006. Web. 16 Oct 2019.

Vancouver:

Bui BH. Thermal rearrangements of heteroatom-bridged polyunsaturated hydrocarbons. [Internet] [Masters thesis]. University of Georgia; 2006. [cited 2019 Oct 16]. Available from: http://purl.galileo.usg.edu/uga_etd/bui_binh_h_200608_ms.

Council of Science Editors:

Bui BH. Thermal rearrangements of heteroatom-bridged polyunsaturated hydrocarbons. [Masters Thesis]. University of Georgia; 2006. Available from: http://purl.galileo.usg.edu/uga_etd/bui_binh_h_200608_ms

2. Kapur, Ashish. Applications of allenes in organic synthesis through cycloadditions; No.

Degree: Science, 2014, Guru Nanak Dev University

No newline

List of Publication: 145-144

Advisors/Committee Members: Ishar, M.P.S..

Subjects/Keywords: allenes; organic synthesis

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APA (6th Edition):

Kapur, A. (2014). Applications of allenes in organic synthesis through cycloadditions; No. (Thesis). Guru Nanak Dev University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/32027

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):

Kapur, Ashish. “Applications of allenes in organic synthesis through cycloadditions; No.” 2014. Thesis, Guru Nanak Dev University. Accessed October 16, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/32027.

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

MLA Handbook (7th Edition):

Kapur, Ashish. “Applications of allenes in organic synthesis through cycloadditions; No.” 2014. Web. 16 Oct 2019.

Vancouver:

Kapur A. Applications of allenes in organic synthesis through cycloadditions; No. [Internet] [Thesis]. Guru Nanak Dev University; 2014. [cited 2019 Oct 16]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/32027.

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

Council of Science Editors:

Kapur A. Applications of allenes in organic synthesis through cycloadditions; No. [Thesis]. Guru Nanak Dev University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/32027

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


University of California – Berkeley

3. LaLonde, Rebecca Lyn K. C. Gold(I)-Catalyzed Nucleophilic Additions.

Degree: Chemistry, 2010, University of California – Berkeley

 The addition of nitrogen, oxygen, and carbon nucleophiles to carbon-carbon unsaturated bonds is an atom economical method of generating structural complexity from simple starting materials.… (more)

Subjects/Keywords: Chemistry, Organic; allenes; aminoauration; gold catalysis

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APA (6th Edition):

LaLonde, R. L. K. C. (2010). Gold(I)-Catalyzed Nucleophilic Additions. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/56p145cg

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):

LaLonde, Rebecca Lyn K C. “Gold(I)-Catalyzed Nucleophilic Additions.” 2010. Thesis, University of California – Berkeley. Accessed October 16, 2019. http://www.escholarship.org/uc/item/56p145cg.

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

MLA Handbook (7th Edition):

LaLonde, Rebecca Lyn K C. “Gold(I)-Catalyzed Nucleophilic Additions.” 2010. Web. 16 Oct 2019.

Vancouver:

LaLonde RLKC. Gold(I)-Catalyzed Nucleophilic Additions. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2019 Oct 16]. Available from: http://www.escholarship.org/uc/item/56p145cg.

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

Council of Science Editors:

LaLonde RLKC. Gold(I)-Catalyzed Nucleophilic Additions. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/56p145cg

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


Duke University

4. Duncan, Alethea. Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles .

Degree: 2011, Duke University

  The importance of nitrogen-containing compounds in human life has drawn us to focus on the preparation of amine derivatives, combined with the limitations associated… (more)

Subjects/Keywords: Chemistry; allenes; Gold-catalyzed; hydroalkoxylation; hydroamination; Hydrofunctionilzation

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APA (6th Edition):

Duncan, A. (2011). Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/5654

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):

Duncan, Alethea. “Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles .” 2011. Thesis, Duke University. Accessed October 16, 2019. http://hdl.handle.net/10161/5654.

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

MLA Handbook (7th Edition):

Duncan, Alethea. “Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles .” 2011. Web. 16 Oct 2019.

Vancouver:

Duncan A. Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles . [Internet] [Thesis]. Duke University; 2011. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10161/5654.

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

Council of Science Editors:

Duncan A. Gold(I)-Catalyzed Hydrofunctionilzations of Allenes with Nitrogen and Oxygen Nucleophiles . [Thesis]. Duke University; 2011. Available from: http://hdl.handle.net/10161/5654

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


Duke University

5. Harris, Robert Joseph. Mechanistic Investigations of Gold(I) Catalyzed Hydrofunctionalizations of C-C Multiple Bonds .

Degree: 2015, Duke University

  Cationic gold(I) complexes containing phosphine and N-heterocyclic carbene based ligands are a powerful catalysts for the hydrofunctionalization of C-C multiple bonds with carbon and… (more)

Subjects/Keywords: Chemistry; allenes; carbene; gold; hydroalkoxylation; hydroamination; racemization

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APA (6th Edition):

Harris, R. J. (2015). Mechanistic Investigations of Gold(I) Catalyzed Hydrofunctionalizations of C-C Multiple Bonds . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/9925

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):

Harris, Robert Joseph. “Mechanistic Investigations of Gold(I) Catalyzed Hydrofunctionalizations of C-C Multiple Bonds .” 2015. Thesis, Duke University. Accessed October 16, 2019. http://hdl.handle.net/10161/9925.

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

MLA Handbook (7th Edition):

Harris, Robert Joseph. “Mechanistic Investigations of Gold(I) Catalyzed Hydrofunctionalizations of C-C Multiple Bonds .” 2015. Web. 16 Oct 2019.

Vancouver:

Harris RJ. Mechanistic Investigations of Gold(I) Catalyzed Hydrofunctionalizations of C-C Multiple Bonds . [Internet] [Thesis]. Duke University; 2015. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10161/9925.

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

Council of Science Editors:

Harris RJ. Mechanistic Investigations of Gold(I) Catalyzed Hydrofunctionalizations of C-C Multiple Bonds . [Thesis]. Duke University; 2015. Available from: http://hdl.handle.net/10161/9925

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

6. Stockton, James David. Cycloadditions of Ketenes with Allenes.

Degree: 1973, North Texas State University

The principle objective of this study is to conduct a definitive investigation into the cycloaddition of allenes and ketenes, with particular emphasis on halogenated ketenes. Advisors/Committee Members: Brady, William Thomas, Norton, S. J..

Subjects/Keywords: cycloadditions; allenes; ketenes

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APA (6th Edition):

Stockton, J. D. (1973). Cycloadditions of Ketenes with Allenes. (Thesis). North Texas State University. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc164080/

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):

Stockton, James David. “Cycloadditions of Ketenes with Allenes.” 1973. Thesis, North Texas State University. Accessed October 16, 2019. https://digital.library.unt.edu/ark:/67531/metadc164080/.

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

MLA Handbook (7th Edition):

Stockton, James David. “Cycloadditions of Ketenes with Allenes.” 1973. Web. 16 Oct 2019.

Vancouver:

Stockton JD. Cycloadditions of Ketenes with Allenes. [Internet] [Thesis]. North Texas State University; 1973. [cited 2019 Oct 16]. Available from: https://digital.library.unt.edu/ark:/67531/metadc164080/.

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

Council of Science Editors:

Stockton JD. Cycloadditions of Ketenes with Allenes. [Thesis]. North Texas State University; 1973. Available from: https://digital.library.unt.edu/ark:/67531/metadc164080/

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


The Ohio State University

7. Mbogo, Grace K. Allenes as Free Radical Acceptors: An Approach to the Polyandranes.

Degree: MS, Chemistry, 2009, The Ohio State University

  This thesis describes the development of a radical cyclization approach to the BC ring system of the C19 quassinoid, 5(S)-polyandrane. The polyandranes are a… (more)

Subjects/Keywords: Chemistry; Free radical cyclization; allenes; polyandranes; organoborane; organotitanium

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APA (6th Edition):

Mbogo, G. K. (2009). Allenes as Free Radical Acceptors: An Approach to the Polyandranes. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1259601041

Chicago Manual of Style (16th Edition):

Mbogo, Grace K. “Allenes as Free Radical Acceptors: An Approach to the Polyandranes.” 2009. Masters Thesis, The Ohio State University. Accessed October 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1259601041.

MLA Handbook (7th Edition):

Mbogo, Grace K. “Allenes as Free Radical Acceptors: An Approach to the Polyandranes.” 2009. Web. 16 Oct 2019.

Vancouver:

Mbogo GK. Allenes as Free Radical Acceptors: An Approach to the Polyandranes. [Internet] [Masters thesis]. The Ohio State University; 2009. [cited 2019 Oct 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1259601041.

Council of Science Editors:

Mbogo GK. Allenes as Free Radical Acceptors: An Approach to the Polyandranes. [Masters Thesis]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1259601041


University of California – Berkeley

8. Zeldin, Rachel Motove. Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C.

Degree: Chemistry, 2011, University of California – Berkeley

 The modern era of synthetic chemistry can be characterized by increased understanding, development and application of transition metal complexes to traditionally organic transformations. While the… (more)

Subjects/Keywords: Chemistry; allenes; flinderole; gold; indole alkaloids; organometallic chemistry; total synthesis

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APA (6th Edition):

Zeldin, R. M. (2011). Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/5437m7h3

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):

Zeldin, Rachel Motove. “Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C.” 2011. Thesis, University of California – Berkeley. Accessed October 16, 2019. http://www.escholarship.org/uc/item/5437m7h3.

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

MLA Handbook (7th Edition):

Zeldin, Rachel Motove. “Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C.” 2011. Web. 16 Oct 2019.

Vancouver:

Zeldin RM. Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2019 Oct 16]. Available from: http://www.escholarship.org/uc/item/5437m7h3.

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

Council of Science Editors:

Zeldin RM. Gold(I)-catalyzed cycloisomerization reactions of allenes: An exploration of ligand effects and the total synthesis of flinderole B and C. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/5437m7h3

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


University of California – Riverside

9. Meyet, Courtney Elizabeth. Copper Catalyzed Three-Component Couplings Form Propargylamines and Quinolines.

Degree: Chemistry, 2013, University of California – Riverside

 A variety of unique small molecule families were created through copper-catalyzed three-component couplings. Propargylamines, 1,3-disubstituted allenes, α,β-unsaturated ketones, and 2,4-disubstituted aryl and alkyl quinolines have… (more)

Subjects/Keywords: Organic chemistry; Chemistry; allenes; dipyrrins; dipyrromethanes; propargylamines; quinolines; unsaturated ketones

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APA (6th Edition):

Meyet, C. E. (2013). Copper Catalyzed Three-Component Couplings Form Propargylamines and Quinolines. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/6626092m

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):

Meyet, Courtney Elizabeth. “Copper Catalyzed Three-Component Couplings Form Propargylamines and Quinolines.” 2013. Thesis, University of California – Riverside. Accessed October 16, 2019. http://www.escholarship.org/uc/item/6626092m.

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

MLA Handbook (7th Edition):

Meyet, Courtney Elizabeth. “Copper Catalyzed Three-Component Couplings Form Propargylamines and Quinolines.” 2013. Web. 16 Oct 2019.

Vancouver:

Meyet CE. Copper Catalyzed Three-Component Couplings Form Propargylamines and Quinolines. [Internet] [Thesis]. University of California – Riverside; 2013. [cited 2019 Oct 16]. Available from: http://www.escholarship.org/uc/item/6626092m.

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

Council of Science Editors:

Meyet CE. Copper Catalyzed Three-Component Couplings Form Propargylamines and Quinolines. [Thesis]. University of California – Riverside; 2013. Available from: http://www.escholarship.org/uc/item/6626092m

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

10. A. Bernasconi. TRANSITION METALS CATALYZED REACTIONS FOR THE SYNTHESIS OF HETEROCYCLIC SYSTEMS.

Degree: 2013, Università degli Studi di Milano

 Pd-catalyzed reactions involving C-N bond formation on easily available substrates containing C-C multiple bonds represent useful methodology to achieve nitrogenated cyclic structures. To this aim… (more)

Subjects/Keywords: palladium; heterocycles; hydroamination; carboamination; allenes; alkynes; Settore CHIM/06 - Chimica Organica

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APA (6th Edition):

Bernasconi, A. (2013). TRANSITION METALS CATALYZED REACTIONS FOR THE SYNTHESIS OF HETEROCYCLIC SYSTEMS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/217537

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):

Bernasconi, A.. “TRANSITION METALS CATALYZED REACTIONS FOR THE SYNTHESIS OF HETEROCYCLIC SYSTEMS.” 2013. Thesis, Università degli Studi di Milano. Accessed October 16, 2019. http://hdl.handle.net/2434/217537.

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

MLA Handbook (7th Edition):

Bernasconi, A.. “TRANSITION METALS CATALYZED REACTIONS FOR THE SYNTHESIS OF HETEROCYCLIC SYSTEMS.” 2013. Web. 16 Oct 2019.

Vancouver:

Bernasconi A. TRANSITION METALS CATALYZED REACTIONS FOR THE SYNTHESIS OF HETEROCYCLIC SYSTEMS. [Internet] [Thesis]. Università degli Studi di Milano; 2013. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2434/217537.

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

Council of Science Editors:

Bernasconi A. TRANSITION METALS CATALYZED REACTIONS FOR THE SYNTHESIS OF HETEROCYCLIC SYSTEMS. [Thesis]. Università degli Studi di Milano; 2013. Available from: http://hdl.handle.net/2434/217537

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


University of Cambridge

11. Poh, Jian Siang. Coupling reactions using flow-generated diazo compounds.

Degree: PhD, 2017, University of Cambridge

 In recent years, the exploitation of flow technologies as an enabling tool to access unique chemical reactivity has flourished. This dissertation describes the utilisation of… (more)

Subjects/Keywords: allenes; copper; diazo compounds; flow chemistry; coupling reactions; asymmetric catalysis; photochemistry

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

APA (6th Edition):

Poh, J. S. (2017). Coupling reactions using flow-generated diazo compounds. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/268223 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744265

Chicago Manual of Style (16th Edition):

Poh, Jian Siang. “Coupling reactions using flow-generated diazo compounds.” 2017. Doctoral Dissertation, University of Cambridge. Accessed October 16, 2019. https://www.repository.cam.ac.uk/handle/1810/268223 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744265.

MLA Handbook (7th Edition):

Poh, Jian Siang. “Coupling reactions using flow-generated diazo compounds.” 2017. Web. 16 Oct 2019.

Vancouver:

Poh JS. Coupling reactions using flow-generated diazo compounds. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2019 Oct 16]. Available from: https://www.repository.cam.ac.uk/handle/1810/268223 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744265.

Council of Science Editors:

Poh JS. Coupling reactions using flow-generated diazo compounds. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/268223 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744265


Virginia Tech

12. Snead, Russell Franklin. Development of Novel, Regioselective Borylation Protocols.

Degree: PhD, Chemistry, 2018, Virginia Tech

 Organoboron compounds are highly valued synthetic intermediates due to their diverse array of reactivity, which is often utilized in the synthesis of valuable organic molecules.… (more)

Subjects/Keywords: borylation; transition metal-catalyzed; transition metal-free; allenes; alkynamides

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

APA (6th Edition):

Snead, R. F. (2018). Development of Novel, Regioselective Borylation Protocols. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/85003

Chicago Manual of Style (16th Edition):

Snead, Russell Franklin. “Development of Novel, Regioselective Borylation Protocols.” 2018. Doctoral Dissertation, Virginia Tech. Accessed October 16, 2019. http://hdl.handle.net/10919/85003.

MLA Handbook (7th Edition):

Snead, Russell Franklin. “Development of Novel, Regioselective Borylation Protocols.” 2018. Web. 16 Oct 2019.

Vancouver:

Snead RF. Development of Novel, Regioselective Borylation Protocols. [Internet] [Doctoral dissertation]. Virginia Tech; 2018. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10919/85003.

Council of Science Editors:

Snead RF. Development of Novel, Regioselective Borylation Protocols. [Doctoral Dissertation]. Virginia Tech; 2018. Available from: http://hdl.handle.net/10919/85003


University of Cambridge

13. Poh, Jian Siang. Coupling reactions using flow-generated diazo compounds .

Degree: 2017, University of Cambridge

 In recent years, the exploitation of flow technologies as an enabling tool to access unique chemical reactivity has flourished. This dissertation describes the utilisation of… (more)

Subjects/Keywords: allenes; copper; diazo compounds; flow chemistry; coupling reactions; asymmetric catalysis; photochemistry

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

APA (6th Edition):

Poh, J. S. (2017). Coupling reactions using flow-generated diazo compounds . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/268223

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):

Poh, Jian Siang. “Coupling reactions using flow-generated diazo compounds .” 2017. Thesis, University of Cambridge. Accessed October 16, 2019. https://www.repository.cam.ac.uk/handle/1810/268223.

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

MLA Handbook (7th Edition):

Poh, Jian Siang. “Coupling reactions using flow-generated diazo compounds .” 2017. Web. 16 Oct 2019.

Vancouver:

Poh JS. Coupling reactions using flow-generated diazo compounds . [Internet] [Thesis]. University of Cambridge; 2017. [cited 2019 Oct 16]. Available from: https://www.repository.cam.ac.uk/handle/1810/268223.

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

Council of Science Editors:

Poh JS. Coupling reactions using flow-generated diazo compounds . [Thesis]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/268223

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


University of Illinois – Chicago

14. Sabbasani, Venkata Reddy. Oxidative Transformations of Allenes (Part I) and Enyne Ring-Closing Metathesis (Part II).

Degree: 2016, University of Illinois – Chicago

 Exploration of new reactivity of silyl-substituted allenes along with the corresponding alkyl-substituted allenes under conditions with various oxidants and/or enophiles to induce nitration, Alder ene… (more)

Subjects/Keywords: Oxidation of Allenes; Nitration of Silylallenes/Allenylsilanes; Dimerization of Silylallenes/Allenylsilanes; Ene Reaction of Allenes; Enyne Ring-Closing Metathesis; Ruthenium Alkylidenes; Tetrahydropyranopyridines

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APA (6th Edition):

Sabbasani, V. R. (2016). Oxidative Transformations of Allenes (Part I) and Enyne Ring-Closing Metathesis (Part II). (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/20926

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):

Sabbasani, Venkata Reddy. “Oxidative Transformations of Allenes (Part I) and Enyne Ring-Closing Metathesis (Part II).” 2016. Thesis, University of Illinois – Chicago. Accessed October 16, 2019. http://hdl.handle.net/10027/20926.

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

MLA Handbook (7th Edition):

Sabbasani, Venkata Reddy. “Oxidative Transformations of Allenes (Part I) and Enyne Ring-Closing Metathesis (Part II).” 2016. Web. 16 Oct 2019.

Vancouver:

Sabbasani VR. Oxidative Transformations of Allenes (Part I) and Enyne Ring-Closing Metathesis (Part II). [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10027/20926.

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

Council of Science Editors:

Sabbasani VR. Oxidative Transformations of Allenes (Part I) and Enyne Ring-Closing Metathesis (Part II). [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/20926

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

15. Vanitcha, Avassaya. New ligands for asymmetric catalysis from allenes : Nouveaux ligands en catalyse asymétrique par des allènes.

Degree: Docteur es, Chimie Moléculaire, 2015, Université Pierre et Marie Curie – Paris VI

Ce travail de thèse décrit la synthèse de nouveaux ligands chiraux pour des applications en catalyse asymétrique. Nous avons ainsi synthétisé différents allènes chiraux possédant… (more)

Subjects/Keywords: Allènes; Catalyse à l'or; Phosphine; Carbène d'or; Cycloisomérisations; Chiralité; Allenes; Chirality; Gold-catalyzed; 541.2

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APA (6th Edition):

Vanitcha, A. (2015). New ligands for asymmetric catalysis from allenes : Nouveaux ligands en catalyse asymétrique par des allènes. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2015PA066714

Chicago Manual of Style (16th Edition):

Vanitcha, Avassaya. “New ligands for asymmetric catalysis from allenes : Nouveaux ligands en catalyse asymétrique par des allènes.” 2015. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 16, 2019. http://www.theses.fr/2015PA066714.

MLA Handbook (7th Edition):

Vanitcha, Avassaya. “New ligands for asymmetric catalysis from allenes : Nouveaux ligands en catalyse asymétrique par des allènes.” 2015. Web. 16 Oct 2019.

Vancouver:

Vanitcha A. New ligands for asymmetric catalysis from allenes : Nouveaux ligands en catalyse asymétrique par des allènes. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. [cited 2019 Oct 16]. Available from: http://www.theses.fr/2015PA066714.

Council of Science Editors:

Vanitcha A. New ligands for asymmetric catalysis from allenes : Nouveaux ligands en catalyse asymétrique par des allènes. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. Available from: http://www.theses.fr/2015PA066714

16. Duran Galvan, Maria. I. Studies on the Metal-Catalyzed Cycloadditions of Isocyanates and Unsaturated Systems and II. Chromium-Catalyzed Synthesis of 1,3-Butadienes via (Silylmethyl)allenes.

Degree: 2011, Texas A&M University

 Metal-catalyzed cycloadditions of alkynes with isocyanates or nitriles are valuable tools for the synthesis of complex carbocycles and heterocycles. Although this transformation has been studied… (more)

Subjects/Keywords: cylcoadditions; isocyanates; chromium; allenes; dienes

…1 1 11 24 25 2. CHROMIUM-CATALYZED SYNTHESIS OF (SILYLMETHYL)ALLENES AND 1,3… …with functional groups other than alkynes (such as dienes, allenes and vinyl… …allenes could be used for this transformation, expecting a higher reactivity than olefins under… …this conditions. 1.2.3. Synthesis and [2+2+2] cycloaddition of allenes with… …isocyanates Allenes are known to undergo [2+2+2] cycloaddition reactions with alkynes in… 

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APA (6th Edition):

Duran Galvan, M. (2011). I. Studies on the Metal-Catalyzed Cycloadditions of Isocyanates and Unsaturated Systems and II. Chromium-Catalyzed Synthesis of 1,3-Butadienes via (Silylmethyl)allenes. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-10142

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):

Duran Galvan, Maria. “I. Studies on the Metal-Catalyzed Cycloadditions of Isocyanates and Unsaturated Systems and II. Chromium-Catalyzed Synthesis of 1,3-Butadienes via (Silylmethyl)allenes.” 2011. Thesis, Texas A&M University. Accessed October 16, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-10142.

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

MLA Handbook (7th Edition):

Duran Galvan, Maria. “I. Studies on the Metal-Catalyzed Cycloadditions of Isocyanates and Unsaturated Systems and II. Chromium-Catalyzed Synthesis of 1,3-Butadienes via (Silylmethyl)allenes.” 2011. Web. 16 Oct 2019.

Vancouver:

Duran Galvan M. I. Studies on the Metal-Catalyzed Cycloadditions of Isocyanates and Unsaturated Systems and II. Chromium-Catalyzed Synthesis of 1,3-Butadienes via (Silylmethyl)allenes. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-10142.

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

Council of Science Editors:

Duran Galvan M. I. Studies on the Metal-Catalyzed Cycloadditions of Isocyanates and Unsaturated Systems and II. Chromium-Catalyzed Synthesis of 1,3-Butadienes via (Silylmethyl)allenes. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-10142

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


Univerzitet u Beogradu

17. Petković, Miloš R., 1980-. Reakcije alena i nukleofila katalizovane paladijumovim kompleksima.

Degree: Hemijski fakultet, 2016, Univerzitet u Beogradu

Hemija - Organska hemija / Chemistry - Organic chemistry

U sklopu ove doktorske teze proučavane su transformacije alena u prisustvu paladijumovih kompleksa, a posebno reaktivnost… (more)

Subjects/Keywords: allenes; π-allylpalladium; allyl acetates; imidazo[1; 2-a]pyridine; synthesis; isomerization; cyclization

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APA (6th Edition):

Petković, Miloš R., 1. (2016). Reakcije alena i nukleofila katalizovane paladijumovim kompleksima. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:12522/bdef:Content/get

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):

Petković, Miloš R., 1980-. “Reakcije alena i nukleofila katalizovane paladijumovim kompleksima.” 2016. Thesis, Univerzitet u Beogradu. Accessed October 16, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:12522/bdef:Content/get.

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

MLA Handbook (7th Edition):

Petković, Miloš R., 1980-. “Reakcije alena i nukleofila katalizovane paladijumovim kompleksima.” 2016. Web. 16 Oct 2019.

Vancouver:

Petković, Miloš R. 1. Reakcije alena i nukleofila katalizovane paladijumovim kompleksima. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Oct 16]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12522/bdef:Content/get.

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

Council of Science Editors:

Petković, Miloš R. 1. Reakcije alena i nukleofila katalizovane paladijumovim kompleksima. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:12522/bdef:Content/get

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


East Tennessee State University

18. Kamga, Mark-Henry Mbahmi. Novel Strategy for the Synthesis of Allenes.

Degree: MS, Chemistry, 2009, East Tennessee State University

Allenes are very important chemical reagents in organic synthesis. Due to their high reactivity, they have been extensively used to carry out a variety… (more)

Subjects/Keywords: allenes; phloroglucinols; Eschenmoser fragmentation; tosylhydrazones; Chemistry; Organic Chemistry; Physical Sciences and Mathematics

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APA (6th Edition):

Kamga, M. M. (2009). Novel Strategy for the Synthesis of Allenes. (Masters Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/1797

Chicago Manual of Style (16th Edition):

Kamga, Mark-Henry Mbahmi. “Novel Strategy for the Synthesis of Allenes.” 2009. Masters Thesis, East Tennessee State University. Accessed October 16, 2019. https://dc.etsu.edu/etd/1797.

MLA Handbook (7th Edition):

Kamga, Mark-Henry Mbahmi. “Novel Strategy for the Synthesis of Allenes.” 2009. Web. 16 Oct 2019.

Vancouver:

Kamga MM. Novel Strategy for the Synthesis of Allenes. [Internet] [Masters thesis]. East Tennessee State University; 2009. [cited 2019 Oct 16]. Available from: https://dc.etsu.edu/etd/1797.

Council of Science Editors:

Kamga MM. Novel Strategy for the Synthesis of Allenes. [Masters Thesis]. East Tennessee State University; 2009. Available from: https://dc.etsu.edu/etd/1797


Universitat Rovira i Virgili

19. Corro Morón, Macarena. Novel Strategies for the Syntheses of Sphingosine Kinase Inhibitors, b-Fluoroamines and Enantioenriched Allenes.

Degree: Departament de Química Analítica i Química Orgànica, 2018, Universitat Rovira i Virgili

 Sphingolipids play a central role in numerous biological and physiological processes and they are converted into each other through the action of enzymes. Ceramide, sphingosine… (more)

Subjects/Keywords: Esfingolípids; Fluoroamines; Al·lens; Esfingolípidos; Fluoroaminas; Alenos; Sphingolipids; Fluoroamines; Allenes; Ciències; 5; 54; 542; 547

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APA (6th Edition):

Corro Morón, M. (2018). Novel Strategies for the Syntheses of Sphingosine Kinase Inhibitors, b-Fluoroamines and Enantioenriched Allenes. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/665123

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):

Corro Morón, Macarena. “Novel Strategies for the Syntheses of Sphingosine Kinase Inhibitors, b-Fluoroamines and Enantioenriched Allenes.” 2018. Thesis, Universitat Rovira i Virgili. Accessed October 16, 2019. http://hdl.handle.net/10803/665123.

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

MLA Handbook (7th Edition):

Corro Morón, Macarena. “Novel Strategies for the Syntheses of Sphingosine Kinase Inhibitors, b-Fluoroamines and Enantioenriched Allenes.” 2018. Web. 16 Oct 2019.

Vancouver:

Corro Morón M. Novel Strategies for the Syntheses of Sphingosine Kinase Inhibitors, b-Fluoroamines and Enantioenriched Allenes. [Internet] [Thesis]. Universitat Rovira i Virgili; 2018. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10803/665123.

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

Council of Science Editors:

Corro Morón M. Novel Strategies for the Syntheses of Sphingosine Kinase Inhibitors, b-Fluoroamines and Enantioenriched Allenes. [Thesis]. Universitat Rovira i Virgili; 2018. Available from: http://hdl.handle.net/10803/665123

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


University of Minnesota

20. Goebel, Erik S. Toward a total synthesis of Englerin A.

Degree: PhD, Chemistry, 2014, University of Minnesota

 Englerin A is a guiane sesquiterpenoid isolated from the spurred potato-bush Phyllanthus engleri that has shown potent and selective activity against renal cancer cell lines.… (more)

Subjects/Keywords: Allenes; Diels-Alder; Englerin A; Retro-Michael fragmentation; Siloxyfuran; Total synthesis; Chemistry

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APA (6th Edition):

Goebel, E. S. (2014). Toward a total synthesis of Englerin A. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/172141

Chicago Manual of Style (16th Edition):

Goebel, Erik S. “Toward a total synthesis of Englerin A.” 2014. Doctoral Dissertation, University of Minnesota. Accessed October 16, 2019. http://hdl.handle.net/11299/172141.

MLA Handbook (7th Edition):

Goebel, Erik S. “Toward a total synthesis of Englerin A.” 2014. Web. 16 Oct 2019.

Vancouver:

Goebel ES. Toward a total synthesis of Englerin A. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/11299/172141.

Council of Science Editors:

Goebel ES. Toward a total synthesis of Englerin A. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/172141


Boston College

21. Sieber, Joshua Daniel. The tandem catalytic asymmetric allene diboration/imine allylation and the asymmetric transition-metal-catalyzed conjugate allylation of activated enones.

Degree: PhD, Chemistry, 2008, Boston College

 Described herein are methods for asymmetric allylation. Chapter 1 describes the scope of the Pd-catalyzed asymmetric diboration of prochiral allenes. The products of this process… (more)

Subjects/Keywords: diboration; conjugate allylation; allenes; asymmetric catalysis

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APA (6th Edition):

Sieber, J. D. (2008). The tandem catalytic asymmetric allene diboration/imine allylation and the asymmetric transition-metal-catalyzed conjugate allylation of activated enones. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101741

Chicago Manual of Style (16th Edition):

Sieber, Joshua Daniel. “The tandem catalytic asymmetric allene diboration/imine allylation and the asymmetric transition-metal-catalyzed conjugate allylation of activated enones.” 2008. Doctoral Dissertation, Boston College. Accessed October 16, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101741.

MLA Handbook (7th Edition):

Sieber, Joshua Daniel. “The tandem catalytic asymmetric allene diboration/imine allylation and the asymmetric transition-metal-catalyzed conjugate allylation of activated enones.” 2008. Web. 16 Oct 2019.

Vancouver:

Sieber JD. The tandem catalytic asymmetric allene diboration/imine allylation and the asymmetric transition-metal-catalyzed conjugate allylation of activated enones. [Internet] [Doctoral dissertation]. Boston College; 2008. [cited 2019 Oct 16]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101741.

Council of Science Editors:

Sieber JD. The tandem catalytic asymmetric allene diboration/imine allylation and the asymmetric transition-metal-catalyzed conjugate allylation of activated enones. [Doctoral Dissertation]. Boston College; 2008. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101741


University of Oxford

22. Feast, George C. Aziridinations of tethered allenes.

Degree: PhD, 2011, University of Oxford

 This thesis describes the synthesis and reactivity of previously unprecedented bicyclic methylene aziridines via rhodium(II) catalysed cyclisation of α-allenic N-tosyloxycarbamates. These aziridines undergo reaction with… (more)

Subjects/Keywords: 547.59; Organic chemistry; Organic synthesis; Physical Sciences; Chemistry & allied sciences; Synthetic organic chemistry; Organometallic Chemistry; aziridines; allenes; rhodium; carbamates; sulfamates

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APA (6th Edition):

Feast, G. C. (2011). Aziridinations of tethered allenes. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:9b7b1fa7-c2fd-4cf1-94f8-333504332d7d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558554

Chicago Manual of Style (16th Edition):

Feast, George C. “Aziridinations of tethered allenes.” 2011. Doctoral Dissertation, University of Oxford. Accessed October 16, 2019. http://ora.ox.ac.uk/objects/uuid:9b7b1fa7-c2fd-4cf1-94f8-333504332d7d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558554.

MLA Handbook (7th Edition):

Feast, George C. “Aziridinations of tethered allenes.” 2011. Web. 16 Oct 2019.

Vancouver:

Feast GC. Aziridinations of tethered allenes. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Oct 16]. Available from: http://ora.ox.ac.uk/objects/uuid:9b7b1fa7-c2fd-4cf1-94f8-333504332d7d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558554.

Council of Science Editors:

Feast GC. Aziridinations of tethered allenes. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:9b7b1fa7-c2fd-4cf1-94f8-333504332d7d ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558554

23. Hu, Ya-Chu. Cu(I)-NHC Catalysed Silylation of Allenes:A Novel Approach towards Vinylsilanes.

Degree: 2014, University of Manchester

 This thesis describes the development of a novel Cu(I)-NHC catalysed silylation of allenes using a commercial available silylborane reagent and the synthesis of a range… (more)

Subjects/Keywords: allenes · copper · homogeneous catalysis · Nheterocyclic carbenes · silylation

…silylation of allenes using a commercial available silylborane reagent and the synthesis of a range… …allenes to afford a variety of vinylsilanes with high efficiency. Allylcoppper intermediates… …synthesised by the protocol of Cu(I)-NHC catalysed silylation of allenes and extension to… …allenes is the most straightforward route. 5 Hydrosilylation and carbosilylation of alkynes are… …comparison, the silylation of allenes is largely dependent on the use of stoichiometric… 

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APA (6th Edition):

Hu, Y. (2014). Cu(I)-NHC Catalysed Silylation of Allenes:A Novel Approach towards Vinylsilanes. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:240023

Chicago Manual of Style (16th Edition):

Hu, Ya-Chu. “Cu(I)-NHC Catalysed Silylation of Allenes:A Novel Approach towards Vinylsilanes.” 2014. Doctoral Dissertation, University of Manchester. Accessed October 16, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:240023.

MLA Handbook (7th Edition):

Hu, Ya-Chu. “Cu(I)-NHC Catalysed Silylation of Allenes:A Novel Approach towards Vinylsilanes.” 2014. Web. 16 Oct 2019.

Vancouver:

Hu Y. Cu(I)-NHC Catalysed Silylation of Allenes:A Novel Approach towards Vinylsilanes. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2019 Oct 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:240023.

Council of Science Editors:

Hu Y. Cu(I)-NHC Catalysed Silylation of Allenes:A Novel Approach towards Vinylsilanes. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:240023


Université Montpellier II

24. Laborde, Coralie. Synthèse de diphosphines et d'acides phosphiniques chiraux : Synthesis of chiral atropisomeric phosphonates and diphosphines.

Degree: Docteur es, Ingénierie moléculaire, 2013, Université Montpellier II

Depuis une trentaine d'année, l'obtention de composés chiraux énantiopurs tient un rôle prépondérant dans la synthèse de molécules biologiquement actives, tout particulièrement dans les domaines… (more)

Subjects/Keywords: Atropoisomérie; Phosphines chirales; Phosphonates chiraux; Allènes; 1; 2; 3-Triazoles; Atropisomery; Chiral phosphines; Chiral phosphonate; Allenes; 1; 2; 3-Triazoles

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APA (6th Edition):

Laborde, C. (2013). Synthèse de diphosphines et d'acides phosphiniques chiraux : Synthesis of chiral atropisomeric phosphonates and diphosphines. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2013MON20256

Chicago Manual of Style (16th Edition):

Laborde, Coralie. “Synthèse de diphosphines et d'acides phosphiniques chiraux : Synthesis of chiral atropisomeric phosphonates and diphosphines.” 2013. Doctoral Dissertation, Université Montpellier II. Accessed October 16, 2019. http://www.theses.fr/2013MON20256.

MLA Handbook (7th Edition):

Laborde, Coralie. “Synthèse de diphosphines et d'acides phosphiniques chiraux : Synthesis of chiral atropisomeric phosphonates and diphosphines.” 2013. Web. 16 Oct 2019.

Vancouver:

Laborde C. Synthèse de diphosphines et d'acides phosphiniques chiraux : Synthesis of chiral atropisomeric phosphonates and diphosphines. [Internet] [Doctoral dissertation]. Université Montpellier II; 2013. [cited 2019 Oct 16]. Available from: http://www.theses.fr/2013MON20256.

Council of Science Editors:

Laborde C. Synthèse de diphosphines et d'acides phosphiniques chiraux : Synthesis of chiral atropisomeric phosphonates and diphosphines. [Doctoral Dissertation]. Université Montpellier II; 2013. Available from: http://www.theses.fr/2013MON20256


University of Waikato

25. Revell, John Bernard. Reactions of Some Cyclomanganated Compounds with C-Nitroso Compounds, Allenes, and Ketenimines .

Degree: 2008, University of Waikato

 eta2-(5-Methoxy-2-acetylphenyl)tetracarbonylmanganese (30) was reacted with 2-methyl-2-nitrosopropane (31) to form 2-acetyl-5-methoxy-N-(tert-butyl)aniline(43) in low yield. Attempts to improve the yield by varying the solvent were unsuccessful. Substrate… (more)

Subjects/Keywords: cyclomanganated; ketenimines; allenes; C-nitroso; cyclometallation; orthomanganated; organometallic

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APA (6th Edition):

Revell, J. B. (2008). Reactions of Some Cyclomanganated Compounds with C-Nitroso Compounds, Allenes, and Ketenimines . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/2275

Chicago Manual of Style (16th Edition):

Revell, John Bernard. “Reactions of Some Cyclomanganated Compounds with C-Nitroso Compounds, Allenes, and Ketenimines .” 2008. Masters Thesis, University of Waikato. Accessed October 16, 2019. http://hdl.handle.net/10289/2275.

MLA Handbook (7th Edition):

Revell, John Bernard. “Reactions of Some Cyclomanganated Compounds with C-Nitroso Compounds, Allenes, and Ketenimines .” 2008. Web. 16 Oct 2019.

Vancouver:

Revell JB. Reactions of Some Cyclomanganated Compounds with C-Nitroso Compounds, Allenes, and Ketenimines . [Internet] [Masters thesis]. University of Waikato; 2008. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10289/2275.

Council of Science Editors:

Revell JB. Reactions of Some Cyclomanganated Compounds with C-Nitroso Compounds, Allenes, and Ketenimines . [Masters Thesis]. University of Waikato; 2008. Available from: http://hdl.handle.net/10289/2275

26. LIU HONGJUN. Bicyclic guanidine catalyzed enantioselective isomerization reactions.

Degree: 2010, National University of Singapore

Subjects/Keywords: Chiral Guanidine; Isomerization; Tandem; Allenes; Alkynes; Itaconimides

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APA (6th Edition):

HONGJUN, L. (2010). Bicyclic guanidine catalyzed enantioselective isomerization reactions. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/18239

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):

HONGJUN, LIU. “Bicyclic guanidine catalyzed enantioselective isomerization reactions.” 2010. Thesis, National University of Singapore. Accessed October 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/18239.

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

MLA Handbook (7th Edition):

HONGJUN, LIU. “Bicyclic guanidine catalyzed enantioselective isomerization reactions.” 2010. Web. 16 Oct 2019.

Vancouver:

HONGJUN L. Bicyclic guanidine catalyzed enantioselective isomerization reactions. [Internet] [Thesis]. National University of Singapore; 2010. [cited 2019 Oct 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/18239.

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

Council of Science Editors:

HONGJUN L. Bicyclic guanidine catalyzed enantioselective isomerization reactions. [Thesis]. National University of Singapore; 2010. Available from: http://scholarbank.nus.edu.sg/handle/10635/18239

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


Boston College

27. Burks, Heather Elizabeth. Transition-metal-catalyzed enantioselective synthesis and functionalization of 1,2- and 1,4-BIS(boronate)esters.

Degree: PhD, Chemistry, 2008, Boston College

 The first examples of an enantioselective allene diboration and diene diboration are reported. The asymmetric palladium-catalyzed allene diboration afforded 1,2- bis(boronate)esters in up to 98%… (more)

Subjects/Keywords: asymmetric diboration; enantioselective diboration of allenes and dienes

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APA (6th Edition):

Burks, H. E. (2008). Transition-metal-catalyzed enantioselective synthesis and functionalization of 1,2- and 1,4-BIS(boronate)esters. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101676

Chicago Manual of Style (16th Edition):

Burks, Heather Elizabeth. “Transition-metal-catalyzed enantioselective synthesis and functionalization of 1,2- and 1,4-BIS(boronate)esters.” 2008. Doctoral Dissertation, Boston College. Accessed October 16, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101676.

MLA Handbook (7th Edition):

Burks, Heather Elizabeth. “Transition-metal-catalyzed enantioselective synthesis and functionalization of 1,2- and 1,4-BIS(boronate)esters.” 2008. Web. 16 Oct 2019.

Vancouver:

Burks HE. Transition-metal-catalyzed enantioselective synthesis and functionalization of 1,2- and 1,4-BIS(boronate)esters. [Internet] [Doctoral dissertation]. Boston College; 2008. [cited 2019 Oct 16]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101676.

Council of Science Editors:

Burks HE. Transition-metal-catalyzed enantioselective synthesis and functionalization of 1,2- and 1,4-BIS(boronate)esters. [Doctoral Dissertation]. Boston College; 2008. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101676

28. Zingales, Nicholas C. Investigation of the Steric and Electronic Properties of 3-Iminophosphine Ligands in Chelated Palladium Allyl Complexes for Use in the Regioselective Hydroamination of Allenes.

Degree: MS, Chemistry, 2013, University of Toledo

 A series of (3-iminophosphine)allylpalladium triflate complexes varying in both steric and electronic features was isolated and characterized. The propensity of the complexes in this series… (more)

Subjects/Keywords: Chemistry; hydroamination; 3-iminophosphine; palladium; intermolecular, anilines; allenes

…4 1-2 Late-transition metal catalyzed hydroamination of substituted allenes . . . . 6… …the regiochemistry of the nitrogen moiety’s addition; when hydroaminating allenes the… …dienes and allenes) and alkynes are more readily hydroaminated than alkenes and… …over the past few years. Although the intramolecular hydroamination of allenes has been… …allenes yields two possible regioisomers. Addition of the amino moiety to the substituted carbon… 

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APA (6th Edition):

Zingales, N. C. (2013). Investigation of the Steric and Electronic Properties of 3-Iminophosphine Ligands in Chelated Palladium Allyl Complexes for Use in the Regioselective Hydroamination of Allenes. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1356544579

Chicago Manual of Style (16th Edition):

Zingales, Nicholas C. “Investigation of the Steric and Electronic Properties of 3-Iminophosphine Ligands in Chelated Palladium Allyl Complexes for Use in the Regioselective Hydroamination of Allenes.” 2013. Masters Thesis, University of Toledo. Accessed October 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1356544579.

MLA Handbook (7th Edition):

Zingales, Nicholas C. “Investigation of the Steric and Electronic Properties of 3-Iminophosphine Ligands in Chelated Palladium Allyl Complexes for Use in the Regioselective Hydroamination of Allenes.” 2013. Web. 16 Oct 2019.

Vancouver:

Zingales NC. Investigation of the Steric and Electronic Properties of 3-Iminophosphine Ligands in Chelated Palladium Allyl Complexes for Use in the Regioselective Hydroamination of Allenes. [Internet] [Masters thesis]. University of Toledo; 2013. [cited 2019 Oct 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1356544579.

Council of Science Editors:

Zingales NC. Investigation of the Steric and Electronic Properties of 3-Iminophosphine Ligands in Chelated Palladium Allyl Complexes for Use in the Regioselective Hydroamination of Allenes. [Masters Thesis]. University of Toledo; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1356544579


Universitat de Girona

29. Haraburda, Ewelina. [2+2+2] cycloaddition reactions involving allenes catalysed by rhodium.

Degree: Departament de Química, 2015, Universitat de Girona

 El desarrollo de nuevos procesos químicos para la formación de enlaces carbono-carbono es un campo importante en química orgánica. Concretamente, la reacción de cicloaddición [2+2+2]… (more)

Subjects/Keywords: Catàlisi de metalls de transició; Transition metal catalysis; Catalizadores metálicos de transición; Cycloaddition; Cicloaddició; Cicloaddición; Allenes; Al·lens; Alenos; Rhodium; Rodio; Rodi; 547

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APA (6th Edition):

Haraburda, E. (2015). [2+2+2] cycloaddition reactions involving allenes catalysed by rhodium. (Thesis). Universitat de Girona. Retrieved from http://hdl.handle.net/10803/328439

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):

Haraburda, Ewelina. “[2+2+2] cycloaddition reactions involving allenes catalysed by rhodium.” 2015. Thesis, Universitat de Girona. Accessed October 16, 2019. http://hdl.handle.net/10803/328439.

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

MLA Handbook (7th Edition):

Haraburda, Ewelina. “[2+2+2] cycloaddition reactions involving allenes catalysed by rhodium.” 2015. Web. 16 Oct 2019.

Vancouver:

Haraburda E. [2+2+2] cycloaddition reactions involving allenes catalysed by rhodium. [Internet] [Thesis]. Universitat de Girona; 2015. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10803/328439.

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

Council of Science Editors:

Haraburda E. [2+2+2] cycloaddition reactions involving allenes catalysed by rhodium. [Thesis]. Universitat de Girona; 2015. Available from: http://hdl.handle.net/10803/328439

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

30. Ondet, Pierrick. Synthèse d'éthers polycycliques par cycloisomérisations catalysées par des acides de Lewis : applications dans le domaine des arômes et parfums. : Synthesis of polycyclic ethers by Lewis acid-catalysed cycloisomerisation for applications in the field of flavour and fragrance.

Degree: Docteur es, Chimie, 2016, Côte d'Azur

Les molécules polycycliques, et notamment les éthers spirocycliques, sont des structures présentant un fort intérêt dans le domaine de la chimie des parfums. Cette thèse… (more)

Subjects/Keywords: Éthers d'énol; Allènes; Triflate de bismuth(III); Polycycles; Éthers spirocycliques; Cycloisomérisation; Catalyse; Odorants; Enol ethers; Allenes; Bismuth(III) triflate; Polycycles; Spirocyclic ethers; Cycloisomerisation; Catalysis; Fragrance chemistry

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APA (6th Edition):

Ondet, P. (2016). Synthèse d'éthers polycycliques par cycloisomérisations catalysées par des acides de Lewis : applications dans le domaine des arômes et parfums. : Synthesis of polycyclic ethers by Lewis acid-catalysed cycloisomerisation for applications in the field of flavour and fragrance. (Doctoral Dissertation). Côte d'Azur. Retrieved from http://www.theses.fr/2016AZUR4075

Chicago Manual of Style (16th Edition):

Ondet, Pierrick. “Synthèse d'éthers polycycliques par cycloisomérisations catalysées par des acides de Lewis : applications dans le domaine des arômes et parfums. : Synthesis of polycyclic ethers by Lewis acid-catalysed cycloisomerisation for applications in the field of flavour and fragrance.” 2016. Doctoral Dissertation, Côte d'Azur. Accessed October 16, 2019. http://www.theses.fr/2016AZUR4075.

MLA Handbook (7th Edition):

Ondet, Pierrick. “Synthèse d'éthers polycycliques par cycloisomérisations catalysées par des acides de Lewis : applications dans le domaine des arômes et parfums. : Synthesis of polycyclic ethers by Lewis acid-catalysed cycloisomerisation for applications in the field of flavour and fragrance.” 2016. Web. 16 Oct 2019.

Vancouver:

Ondet P. Synthèse d'éthers polycycliques par cycloisomérisations catalysées par des acides de Lewis : applications dans le domaine des arômes et parfums. : Synthesis of polycyclic ethers by Lewis acid-catalysed cycloisomerisation for applications in the field of flavour and fragrance. [Internet] [Doctoral dissertation]. Côte d'Azur; 2016. [cited 2019 Oct 16]. Available from: http://www.theses.fr/2016AZUR4075.

Council of Science Editors:

Ondet P. Synthèse d'éthers polycycliques par cycloisomérisations catalysées par des acides de Lewis : applications dans le domaine des arômes et parfums. : Synthesis of polycyclic ethers by Lewis acid-catalysed cycloisomerisation for applications in the field of flavour and fragrance. [Doctoral Dissertation]. Côte d'Azur; 2016. Available from: http://www.theses.fr/2016AZUR4075

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