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You searched for subject:(Allene). Showing records 1 – 30 of 55 total matches.

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Rutgers University

1. Zhang, Yue, 1976-. Formation and reactivity of allenes and spirodiepoxides.

Degree: PhD, Chemistry and Chemical Biology, 2010, Rutgers University

Disclosed are the studies on allene and functionalized medium sized ring synthesis as well as applications of spirodiepoxide based methods. A new method of making… (more)

Subjects/Keywords: Allene – Oxidation; Allene – Reactivity

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APA (6th Edition):

Zhang, Yue, 1. (2010). Formation and reactivity of allenes and spirodiepoxides. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056874

Chicago Manual of Style (16th Edition):

Zhang, Yue, 1976-. “Formation and reactivity of allenes and spirodiepoxides.” 2010. Doctoral Dissertation, Rutgers University. Accessed June 20, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056874.

MLA Handbook (7th Edition):

Zhang, Yue, 1976-. “Formation and reactivity of allenes and spirodiepoxides.” 2010. Web. 20 Jun 2019.

Vancouver:

Zhang, Yue 1. Formation and reactivity of allenes and spirodiepoxides. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Jun 20]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056874.

Council of Science Editors:

Zhang, Yue 1. Formation and reactivity of allenes and spirodiepoxides. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056874


University of Hawaii

2. Waters, William Lincoln. The oxymercuration of allenes.

Degree: PhD, 2009, University of Hawaii

Typescript.

Bibliography: leaves [97]-100.

xi, 100 l illus., tables

Addition of mercuric acetate to allene and the five possible methyl-substituted allenes was carried out in… (more)

Subjects/Keywords: Mercury; Allene

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APA (6th Edition):

Waters, W. L. (2009). The oxymercuration of allenes. (Doctoral Dissertation). University of Hawaii. Retrieved from http://hdl.handle.net/10125/11395

Chicago Manual of Style (16th Edition):

Waters, William Lincoln. “The oxymercuration of allenes.” 2009. Doctoral Dissertation, University of Hawaii. Accessed June 20, 2019. http://hdl.handle.net/10125/11395.

MLA Handbook (7th Edition):

Waters, William Lincoln. “The oxymercuration of allenes.” 2009. Web. 20 Jun 2019.

Vancouver:

Waters WL. The oxymercuration of allenes. [Internet] [Doctoral dissertation]. University of Hawaii; 2009. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/10125/11395.

Council of Science Editors:

Waters WL. The oxymercuration of allenes. [Doctoral Dissertation]. University of Hawaii; 2009. Available from: http://hdl.handle.net/10125/11395


University of Hong Kong

3. Chan, Yu-man. Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation.

Degree: M. Phil., 2015, University of Hong Kong

The pursuit of highly enantioselective reactions for the generation of complex organic molecules with point/axial chirality is everlasting for synthetic organic chemists. Axially chiral vinylallenes… (more)

Subjects/Keywords: Chirality; Allene

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APA (6th Edition):

Chan, Y. (2015). Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. (Masters Thesis). University of Hong Kong. Retrieved from Chan, Y. [陳宇文]. (2015). Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5610943. ; http://dx.doi.org/10.5353/th_b5610943 ; http://hdl.handle.net/10722/246862

Chicago Manual of Style (16th Edition):

Chan, Yu-man. “Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation.” 2015. Masters Thesis, University of Hong Kong. Accessed June 20, 2019. Chan, Y. [陳宇文]. (2015). Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5610943. ; http://dx.doi.org/10.5353/th_b5610943 ; http://hdl.handle.net/10722/246862.

MLA Handbook (7th Edition):

Chan, Yu-man. “Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation.” 2015. Web. 20 Jun 2019.

Vancouver:

Chan Y. Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Jun 20]. Available from: Chan, Y. [陳宇文]. (2015). Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5610943. ; http://dx.doi.org/10.5353/th_b5610943 ; http://hdl.handle.net/10722/246862.

Council of Science Editors:

Chan Y. Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. [Masters Thesis]. University of Hong Kong; 2015. Available from: Chan, Y. [陳宇文]. (2015). Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5610943. ; http://dx.doi.org/10.5353/th_b5610943 ; http://hdl.handle.net/10722/246862


University of Ottawa

4. Shore, Daniel Gordon Michael. I. The Enantioselective Synthesis of Chiral Allenyl Carbonyl Compounds and Their Use as Synthetic Intermediates II. Rhodium-Catalyzed C-H Functionalization: Application to the Synthesis of 3-Carboxylindoles and Attempted Applications to Allenes .

Degree: 2011, University of Ottawa

 Allenes are unique compounds in organic chemistry by virtue of their adjacent, orthogonal π-bonds. While of limited use in and of themselves, some classes of… (more)

Subjects/Keywords: Allene; Rhodium

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APA (6th Edition):

Shore, D. G. M. (2011). I. The Enantioselective Synthesis of Chiral Allenyl Carbonyl Compounds and Their Use as Synthetic Intermediates II. Rhodium-Catalyzed C-H Functionalization: Application to the Synthesis of 3-Carboxylindoles and Attempted Applications to Allenes . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/19891

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):

Shore, Daniel Gordon Michael. “I. The Enantioselective Synthesis of Chiral Allenyl Carbonyl Compounds and Their Use as Synthetic Intermediates II. Rhodium-Catalyzed C-H Functionalization: Application to the Synthesis of 3-Carboxylindoles and Attempted Applications to Allenes .” 2011. Thesis, University of Ottawa. Accessed June 20, 2019. http://hdl.handle.net/10393/19891.

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

MLA Handbook (7th Edition):

Shore, Daniel Gordon Michael. “I. The Enantioselective Synthesis of Chiral Allenyl Carbonyl Compounds and Their Use as Synthetic Intermediates II. Rhodium-Catalyzed C-H Functionalization: Application to the Synthesis of 3-Carboxylindoles and Attempted Applications to Allenes .” 2011. Web. 20 Jun 2019.

Vancouver:

Shore DGM. I. The Enantioselective Synthesis of Chiral Allenyl Carbonyl Compounds and Their Use as Synthetic Intermediates II. Rhodium-Catalyzed C-H Functionalization: Application to the Synthesis of 3-Carboxylindoles and Attempted Applications to Allenes . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/10393/19891.

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

Council of Science Editors:

Shore DGM. I. The Enantioselective Synthesis of Chiral Allenyl Carbonyl Compounds and Their Use as Synthetic Intermediates II. Rhodium-Catalyzed C-H Functionalization: Application to the Synthesis of 3-Carboxylindoles and Attempted Applications to Allenes . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/19891

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


University of Alberta

5. Zhou, Sida. Generation and Trapping of Highly Strained Reactive Intermediate: Ethyl 1,2-Cyclohexadienecarboxylate.

Degree: MS, Department of Chemistry, 2015, University of Alberta

 Highly strained reactive intermediates can initiate chemical reactions and afford unique products. Cyclic allenes are important examples of such intermediates. Within the cyclic allene family,… (more)

Subjects/Keywords: 1,2-cyclohexadiene; cyclic allene

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APA (6th Edition):

Zhou, S. (2015). Generation and Trapping of Highly Strained Reactive Intermediate: Ethyl 1,2-Cyclohexadienecarboxylate. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/w95053154

Chicago Manual of Style (16th Edition):

Zhou, Sida. “Generation and Trapping of Highly Strained Reactive Intermediate: Ethyl 1,2-Cyclohexadienecarboxylate.” 2015. Masters Thesis, University of Alberta. Accessed June 20, 2019. https://era.library.ualberta.ca/files/w95053154.

MLA Handbook (7th Edition):

Zhou, Sida. “Generation and Trapping of Highly Strained Reactive Intermediate: Ethyl 1,2-Cyclohexadienecarboxylate.” 2015. Web. 20 Jun 2019.

Vancouver:

Zhou S. Generation and Trapping of Highly Strained Reactive Intermediate: Ethyl 1,2-Cyclohexadienecarboxylate. [Internet] [Masters thesis]. University of Alberta; 2015. [cited 2019 Jun 20]. Available from: https://era.library.ualberta.ca/files/w95053154.

Council of Science Editors:

Zhou S. Generation and Trapping of Highly Strained Reactive Intermediate: Ethyl 1,2-Cyclohexadienecarboxylate. [Masters Thesis]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/w95053154


University of Hong Kong

6. 陳宇文; Chan, Yu-man. Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation.

Degree: M. Phil., 2015, University of Hong Kong

abstract

Chemistry

Master

Master of Philosophy

Subjects/Keywords: Chirality; Allene

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APA (6th Edition):

陳宇文; Chan, Y. (2015). Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/221185

Chicago Manual of Style (16th Edition):

陳宇文; Chan, Yu-man. “Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation.” 2015. Masters Thesis, University of Hong Kong. Accessed June 20, 2019. http://hdl.handle.net/10722/221185.

MLA Handbook (7th Edition):

陳宇文; Chan, Yu-man. “Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation.” 2015. Web. 20 Jun 2019.

Vancouver:

陳宇文; Chan Y. Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/10722/221185.

Council of Science Editors:

陳宇文; Chan Y. Synthesis of axially chiral vinylallenes, and their subsequent reactions : silver(I) catalyzed enantioselective diels-alder reaction and aerobic oxidation. [Masters Thesis]. University of Hong Kong; 2015. Available from: http://hdl.handle.net/10722/221185


McGill University

7. Ong, Beng Soon. The chemistry of allene oxides.

Degree: PhD, Department of Chemistry, 1976, McGill University

Subjects/Keywords: Allene oxide.

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APA (6th Edition):

Ong, B. S. (1976). The chemistry of allene oxides. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile76191.pdf

Chicago Manual of Style (16th Edition):

Ong, Beng Soon. “The chemistry of allene oxides.” 1976. Doctoral Dissertation, McGill University. Accessed June 20, 2019. http://digitool.library.mcgill.ca/thesisfile76191.pdf.

MLA Handbook (7th Edition):

Ong, Beng Soon. “The chemistry of allene oxides.” 1976. Web. 20 Jun 2019.

Vancouver:

Ong BS. The chemistry of allene oxides. [Internet] [Doctoral dissertation]. McGill University; 1976. [cited 2019 Jun 20]. Available from: http://digitool.library.mcgill.ca/thesisfile76191.pdf.

Council of Science Editors:

Ong BS. The chemistry of allene oxides. [Doctoral Dissertation]. McGill University; 1976. Available from: http://digitool.library.mcgill.ca/thesisfile76191.pdf


University of Kansas

8. Smith, Mary Katherine. Palladium-Catalyzed Synthesis and Racemization of Conjugated Allenynes.

Degree: PhD, Chemistry, 2017, University of Kansas

 Allenes are structurally unique compounds that can possess axial chirality. The most common strategy for allene synthesis is transition metal-catalyzed cross coupling with propargyl electrophiles.… (more)

Subjects/Keywords: Organic chemistry; Allene; Decarboxylation; Racemization

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APA (6th Edition):

Smith, M. K. (2017). Palladium-Catalyzed Synthesis and Racemization of Conjugated Allenynes. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/26029

Chicago Manual of Style (16th Edition):

Smith, Mary Katherine. “Palladium-Catalyzed Synthesis and Racemization of Conjugated Allenynes.” 2017. Doctoral Dissertation, University of Kansas. Accessed June 20, 2019. http://hdl.handle.net/1808/26029.

MLA Handbook (7th Edition):

Smith, Mary Katherine. “Palladium-Catalyzed Synthesis and Racemization of Conjugated Allenynes.” 2017. Web. 20 Jun 2019.

Vancouver:

Smith MK. Palladium-Catalyzed Synthesis and Racemization of Conjugated Allenynes. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/1808/26029.

Council of Science Editors:

Smith MK. Palladium-Catalyzed Synthesis and Racemization of Conjugated Allenynes. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/26029


Rutgers University

9. Cusick, Joseph Ryan, 1982-. Allene cycloisomerization, epoxidation, and applications in total synthesis.

Degree: Chemistry and Chemical Biology, 2011, Rutgers University

Subjects/Keywords: Allene—Synthesis

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APA (6th Edition):

Cusick, Joseph Ryan, 1. (2011). Allene cycloisomerization, epoxidation, and applications in total synthesis. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063389

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):

Cusick, Joseph Ryan, 1982-. “Allene cycloisomerization, epoxidation, and applications in total synthesis.” 2011. Thesis, Rutgers University. Accessed June 20, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063389.

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

MLA Handbook (7th Edition):

Cusick, Joseph Ryan, 1982-. “Allene cycloisomerization, epoxidation, and applications in total synthesis.” 2011. Web. 20 Jun 2019.

Vancouver:

Cusick, Joseph Ryan 1. Allene cycloisomerization, epoxidation, and applications in total synthesis. [Internet] [Thesis]. Rutgers University; 2011. [cited 2019 Jun 20]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063389.

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

Council of Science Editors:

Cusick, Joseph Ryan 1. Allene cycloisomerization, epoxidation, and applications in total synthesis. [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063389

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


University of Illinois – Chicago

10. Lee, Nam-Kyu. Allenylsilane Synthesis and Reactivity of Them (Part I) and Group 11 Metal-Catalyzed Reactions (Part II).

Degree: 2014, University of Illinois – Chicago

 This thesis has two mainparts. Part I is composed oftwo chapterswhich describe new and convenient method for allenylsilane synthesis and formal ene-type reaction of silylallenes… (more)

Subjects/Keywords: Allene; Autoooxydation; Gold; Silver; Aryne; Biaryl

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APA (6th Edition):

Lee, N. (2014). Allenylsilane Synthesis and Reactivity of Them (Part I) and Group 11 Metal-Catalyzed Reactions (Part II). (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/18892

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):

Lee, Nam-Kyu. “Allenylsilane Synthesis and Reactivity of Them (Part I) and Group 11 Metal-Catalyzed Reactions (Part II).” 2014. Thesis, University of Illinois – Chicago. Accessed June 20, 2019. http://hdl.handle.net/10027/18892.

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

MLA Handbook (7th Edition):

Lee, Nam-Kyu. “Allenylsilane Synthesis and Reactivity of Them (Part I) and Group 11 Metal-Catalyzed Reactions (Part II).” 2014. Web. 20 Jun 2019.

Vancouver:

Lee N. Allenylsilane Synthesis and Reactivity of Them (Part I) and Group 11 Metal-Catalyzed Reactions (Part II). [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/10027/18892.

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

Council of Science Editors:

Lee N. Allenylsilane Synthesis and Reactivity of Them (Part I) and Group 11 Metal-Catalyzed Reactions (Part II). [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/18892

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


University of Manchester

11. Rae, James. Copper-catalysed silicon and boron functionalisation of heterocycles and allenes.

Degree: 2015, University of Manchester

 Silicon holds a privileged position in organic chemistry as the carbon-silicon bond can be utilised in many important transformations. As such, developing practical and efficient… (more)

Subjects/Keywords: Copper; Enantioselective; Silicon; Boron; Catalysis; Allene

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APA (6th Edition):

Rae, J. (2015). Copper-catalysed silicon and boron functionalisation of heterocycles and allenes. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:269795

Chicago Manual of Style (16th Edition):

Rae, James. “Copper-catalysed silicon and boron functionalisation of heterocycles and allenes.” 2015. Doctoral Dissertation, University of Manchester. Accessed June 20, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:269795.

MLA Handbook (7th Edition):

Rae, James. “Copper-catalysed silicon and boron functionalisation of heterocycles and allenes.” 2015. Web. 20 Jun 2019.

Vancouver:

Rae J. Copper-catalysed silicon and boron functionalisation of heterocycles and allenes. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Jun 20]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:269795.

Council of Science Editors:

Rae J. Copper-catalysed silicon and boron functionalisation of heterocycles and allenes. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:269795

12. Kim, Hiyun. Allene-based approach to the synthesis of De Novo erythromycinoids.

Degree: Chemistry and Chemical Biology, 2012, Rutgers University

Subjects/Keywords: Allene – Research

…14 2.3. Synthetic Strategy: Bis[Allene] Macrolactone… …15 vii 2.4. Allene Oxidation: Spirodiepoxide (SDE) Chmistry… …16 2.5. Allene Oxidation: Osmylation… …18 2.6. Model Study: Bis[Allene] Macrolactone… …19 2.7. Convergent Synthesis of Bis[Allene] Macrolactone… 

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7 Sample image

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APA (6th Edition):

Kim, H. (2012). Allene-based approach to the synthesis of De Novo erythromycinoids. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064137

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):

Kim, Hiyun. “Allene-based approach to the synthesis of De Novo erythromycinoids.” 2012. Thesis, Rutgers University. Accessed June 20, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064137.

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

MLA Handbook (7th Edition):

Kim, Hiyun. “Allene-based approach to the synthesis of De Novo erythromycinoids.” 2012. Web. 20 Jun 2019.

Vancouver:

Kim H. Allene-based approach to the synthesis of De Novo erythromycinoids. [Internet] [Thesis]. Rutgers University; 2012. [cited 2019 Jun 20]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064137.

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

Council of Science Editors:

Kim H. Allene-based approach to the synthesis of De Novo erythromycinoids. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000064137

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


University of Rochester

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

Degree: PhD, 2009, University of Rochester

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Malona, John A (1981 - ). “I. scandium (III) catalyzed Nazarov cyclization of heteroaryl-vinyl ketones : II. Efforts towards the total synthesis of (±) - rocaglamide via a Nazarov cyclization strategy ; III. Efforts towards the total synthesis of (±) - rocaglamide via an alkoxy allene epoxidation/Nazarov cyclization.” 2009. Doctoral Dissertation, University of Rochester. Accessed June 20, 2019. http://hdl.handle.net/1802/7445.

MLA Handbook (7th Edition):

Malona, John A (1981 - ). “I. scandium (III) catalyzed Nazarov cyclization of heteroaryl-vinyl ketones : II. Efforts towards the total synthesis of (±) - rocaglamide via a Nazarov cyclization strategy ; III. Efforts towards the total synthesis of (±) - rocaglamide via an alkoxy allene epoxidation/Nazarov cyclization.” 2009. Web. 20 Jun 2019.

Vancouver:

Malona JA(-). I. scandium (III) catalyzed Nazarov cyclization of heteroaryl-vinyl ketones : II. Efforts towards the total synthesis of (±) - rocaglamide via a Nazarov cyclization strategy ; III. Efforts towards the total synthesis of (±) - rocaglamide via an alkoxy allene epoxidation/Nazarov cyclization. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/1802/7445.

Council of Science Editors:

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


University of Rochester

14. Spencer, William T. (1979 - ). I. Oxidation-initiated Nazarov cyclization of vinyl alkoxyallenes. II. Efforts toward an improved synthesis of rocaglamide amenable to analog synthesis. III. A convenient cycloaromatization protocol for synthesis of polysubstituted phenol derivatives: method development and mechanistic studies.

Degree: PhD, 2013, University of Rochester

 I. Oxidation-Initiated Nazarov Cyclization of Vinyl Alkoxyallenes. This chapter describes the development of an oxidation-triggered Nazarov cyclization of vinyl alkoxyallenes. First, we discuss how a… (more)

Subjects/Keywords: Allene; Cycloaromatization; Cycloisomerization; Electrocyclization; Nazarov; Rocaglamide

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

APA (6th Edition):

Spencer, W. T. (. -. ). (2013). I. Oxidation-initiated Nazarov cyclization of vinyl alkoxyallenes. II. Efforts toward an improved synthesis of rocaglamide amenable to analog synthesis. III. A convenient cycloaromatization protocol for synthesis of polysubstituted phenol derivatives: method development and mechanistic studies. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/26809

Chicago Manual of Style (16th Edition):

Spencer, William T (1979 - ). “I. Oxidation-initiated Nazarov cyclization of vinyl alkoxyallenes. II. Efforts toward an improved synthesis of rocaglamide amenable to analog synthesis. III. A convenient cycloaromatization protocol for synthesis of polysubstituted phenol derivatives: method development and mechanistic studies.” 2013. Doctoral Dissertation, University of Rochester. Accessed June 20, 2019. http://hdl.handle.net/1802/26809.

MLA Handbook (7th Edition):

Spencer, William T (1979 - ). “I. Oxidation-initiated Nazarov cyclization of vinyl alkoxyallenes. II. Efforts toward an improved synthesis of rocaglamide amenable to analog synthesis. III. A convenient cycloaromatization protocol for synthesis of polysubstituted phenol derivatives: method development and mechanistic studies.” 2013. Web. 20 Jun 2019.

Vancouver:

Spencer WT(-). I. Oxidation-initiated Nazarov cyclization of vinyl alkoxyallenes. II. Efforts toward an improved synthesis of rocaglamide amenable to analog synthesis. III. A convenient cycloaromatization protocol for synthesis of polysubstituted phenol derivatives: method development and mechanistic studies. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/1802/26809.

Council of Science Editors:

Spencer WT(-). I. Oxidation-initiated Nazarov cyclization of vinyl alkoxyallenes. II. Efforts toward an improved synthesis of rocaglamide amenable to analog synthesis. III. A convenient cycloaromatization protocol for synthesis of polysubstituted phenol derivatives: method development and mechanistic studies. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/26809


University of Manchester

15. Rae, James. Copper-catalysed silicon and boron functionalisation of heterocycles and allenes.

Degree: PhD, 2015, University of Manchester

 Silicon holds a privileged position in organic chemistry as the carbon-silicon bond can be utilised in many important transformations. As such, developing practical and efficient… (more)

Subjects/Keywords: 547; Catalysis; Allene; Boron; Copper; Enantioselective; Silicon

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APA (6th Edition):

Rae, J. (2015). Copper-catalysed silicon and boron functionalisation of heterocycles and allenes. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/coppercatalysed-silicon-and-boron-functionalisation-of-heterocycles-and-allenes(a86718c0-18b4-4092-a2bd-b978797153db).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727830

Chicago Manual of Style (16th Edition):

Rae, James. “Copper-catalysed silicon and boron functionalisation of heterocycles and allenes.” 2015. Doctoral Dissertation, University of Manchester. Accessed June 20, 2019. https://www.research.manchester.ac.uk/portal/en/theses/coppercatalysed-silicon-and-boron-functionalisation-of-heterocycles-and-allenes(a86718c0-18b4-4092-a2bd-b978797153db).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727830.

MLA Handbook (7th Edition):

Rae, James. “Copper-catalysed silicon and boron functionalisation of heterocycles and allenes.” 2015. Web. 20 Jun 2019.

Vancouver:

Rae J. Copper-catalysed silicon and boron functionalisation of heterocycles and allenes. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Jun 20]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/coppercatalysed-silicon-and-boron-functionalisation-of-heterocycles-and-allenes(a86718c0-18b4-4092-a2bd-b978797153db).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727830.

Council of Science Editors:

Rae J. Copper-catalysed silicon and boron functionalisation of heterocycles and allenes. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/coppercatalysed-silicon-and-boron-functionalisation-of-heterocycles-and-allenes(a86718c0-18b4-4092-a2bd-b978797153db).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.727830


The Ohio State University

16. Bleiholder, Roland Francis. I. Capture reactions of carbenes by cumulenes : II. Additions of azides to allenes.

Degree: PhD, Graduate School, 1966, The Ohio State University

Subjects/Keywords: Chemistry; Carbenes; Azides; Allene

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APA (6th Edition):

Bleiholder, R. F. (1966). I. Capture reactions of carbenes by cumulenes : II. Additions of azides to allenes. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1486633062998973

Chicago Manual of Style (16th Edition):

Bleiholder, Roland Francis. “I. Capture reactions of carbenes by cumulenes : II. Additions of azides to allenes.” 1966. Doctoral Dissertation, The Ohio State University. Accessed June 20, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1486633062998973.

MLA Handbook (7th Edition):

Bleiholder, Roland Francis. “I. Capture reactions of carbenes by cumulenes : II. Additions of azides to allenes.” 1966. Web. 20 Jun 2019.

Vancouver:

Bleiholder RF. I. Capture reactions of carbenes by cumulenes : II. Additions of azides to allenes. [Internet] [Doctoral dissertation]. The Ohio State University; 1966. [cited 2019 Jun 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486633062998973.

Council of Science Editors:

Bleiholder RF. I. Capture reactions of carbenes by cumulenes : II. Additions of azides to allenes. [Doctoral Dissertation]. The Ohio State University; 1966. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1486633062998973


UCLA

17. Martin, Tioga Jarrett. Phosphine Catalysis using Allenoates with pro-Nucleophiles or Arylidenes; Development of an Asymetric Phosphine Catalyst; and Allenes as π-Ligands in Copper-Mediated Cross-Coupling.

Degree: Chemistry, 2014, UCLA

 The unique characteristics of 1,2-dienes have proven to be a dynamic and ever growing field of study in organic chemistry. Allenes have been manipulated into… (more)

Subjects/Keywords: Organic chemistry; Allene; Asymetric; Catalysis; Copper; Phosphine; Synthesis

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APA (6th Edition):

Martin, T. J. (2014). Phosphine Catalysis using Allenoates with pro-Nucleophiles or Arylidenes; Development of an Asymetric Phosphine Catalyst; and Allenes as π-Ligands in Copper-Mediated Cross-Coupling. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9cz290fh

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):

Martin, Tioga Jarrett. “Phosphine Catalysis using Allenoates with pro-Nucleophiles or Arylidenes; Development of an Asymetric Phosphine Catalyst; and Allenes as π-Ligands in Copper-Mediated Cross-Coupling.” 2014. Thesis, UCLA. Accessed June 20, 2019. http://www.escholarship.org/uc/item/9cz290fh.

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

MLA Handbook (7th Edition):

Martin, Tioga Jarrett. “Phosphine Catalysis using Allenoates with pro-Nucleophiles or Arylidenes; Development of an Asymetric Phosphine Catalyst; and Allenes as π-Ligands in Copper-Mediated Cross-Coupling.” 2014. Web. 20 Jun 2019.

Vancouver:

Martin TJ. Phosphine Catalysis using Allenoates with pro-Nucleophiles or Arylidenes; Development of an Asymetric Phosphine Catalyst; and Allenes as π-Ligands in Copper-Mediated Cross-Coupling. [Internet] [Thesis]. UCLA; 2014. [cited 2019 Jun 20]. Available from: http://www.escholarship.org/uc/item/9cz290fh.

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

Council of Science Editors:

Martin TJ. Phosphine Catalysis using Allenoates with pro-Nucleophiles or Arylidenes; Development of an Asymetric Phosphine Catalyst; and Allenes as π-Ligands in Copper-Mediated Cross-Coupling. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/9cz290fh

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


UCLA

18. Pham, Hung Viet. Theoretical Investigations of Cycloadditions and Subsequent Transformations Involving Allenes and Arenes to Form Complex Polycycles.

Degree: Chemistry, 2015, UCLA

 This dissertation is a culmination of research projects that combine the utility of computational methods with the practicality of experiments in order to investigate a… (more)

Subjects/Keywords: Chemistry; Allene; Computational Chemistry; Cycloaddition; Diels-Alder; Physical Organic Chemistry

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APA (6th Edition):

Pham, H. V. (2015). Theoretical Investigations of Cycloadditions and Subsequent Transformations Involving Allenes and Arenes to Form Complex Polycycles. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/2f1663fp

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):

Pham, Hung Viet. “Theoretical Investigations of Cycloadditions and Subsequent Transformations Involving Allenes and Arenes to Form Complex Polycycles.” 2015. Thesis, UCLA. Accessed June 20, 2019. http://www.escholarship.org/uc/item/2f1663fp.

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

MLA Handbook (7th Edition):

Pham, Hung Viet. “Theoretical Investigations of Cycloadditions and Subsequent Transformations Involving Allenes and Arenes to Form Complex Polycycles.” 2015. Web. 20 Jun 2019.

Vancouver:

Pham HV. Theoretical Investigations of Cycloadditions and Subsequent Transformations Involving Allenes and Arenes to Form Complex Polycycles. [Internet] [Thesis]. UCLA; 2015. [cited 2019 Jun 20]. Available from: http://www.escholarship.org/uc/item/2f1663fp.

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

Council of Science Editors:

Pham HV. Theoretical Investigations of Cycloadditions and Subsequent Transformations Involving Allenes and Arenes to Form Complex Polycycles. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/2f1663fp

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


Duke University

19. Butler, Kristina LeAnne. Gold(I) and Platinum(II)-Catalyzed Hydrofunctionalization of Allenes and Alkenes with Carbon and Nitrogen Nucleophiles .

Degree: 2012, Duke University

  The wide-spread occurrence of biologically active nitrogen-containing heterocycles and allylic amines inspired us to develop atom-economical methods for their syntheses. A cationic gold(I) N-heterocyclic… (more)

Subjects/Keywords: Chemistry; allene; gold(I); hydroamination; hydroarylation; platinum(II)

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APA (6th Edition):

Butler, K. L. (2012). Gold(I) and Platinum(II)-Catalyzed Hydrofunctionalization of Allenes and Alkenes with Carbon and Nitrogen Nucleophiles . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/5533

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):

Butler, Kristina LeAnne. “Gold(I) and Platinum(II)-Catalyzed Hydrofunctionalization of Allenes and Alkenes with Carbon and Nitrogen Nucleophiles .” 2012. Thesis, Duke University. Accessed June 20, 2019. http://hdl.handle.net/10161/5533.

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

MLA Handbook (7th Edition):

Butler, Kristina LeAnne. “Gold(I) and Platinum(II)-Catalyzed Hydrofunctionalization of Allenes and Alkenes with Carbon and Nitrogen Nucleophiles .” 2012. Web. 20 Jun 2019.

Vancouver:

Butler KL. Gold(I) and Platinum(II)-Catalyzed Hydrofunctionalization of Allenes and Alkenes with Carbon and Nitrogen Nucleophiles . [Internet] [Thesis]. Duke University; 2012. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/10161/5533.

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

Council of Science Editors:

Butler KL. Gold(I) and Platinum(II)-Catalyzed Hydrofunctionalization of Allenes and Alkenes with Carbon and Nitrogen Nucleophiles . [Thesis]. Duke University; 2012. Available from: http://hdl.handle.net/10161/5533

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


University of Oxford

20. Li, Meiling. Palladium catalysed allene carbocyclisation.

Degree: PhD, 2010, University of Oxford

 In this thesis, firstly, a Pd-catalysed diastereoselective carbocyclisation of allenes with aryl halides or vinyl iodides was designed and developed to form arylative or vinylative… (more)

Subjects/Keywords: 547.6; Organic chemistry; Organic synthesis; Palladium; Allene; Carbocyclisation

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APA (6th Edition):

Li, M. (2010). Palladium catalysed allene carbocyclisation. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:747420b6-c11f-451c-83c7-fa9fca5f7752 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543528

Chicago Manual of Style (16th Edition):

Li, Meiling. “Palladium catalysed allene carbocyclisation.” 2010. Doctoral Dissertation, University of Oxford. Accessed June 20, 2019. http://ora.ox.ac.uk/objects/uuid:747420b6-c11f-451c-83c7-fa9fca5f7752 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543528.

MLA Handbook (7th Edition):

Li, Meiling. “Palladium catalysed allene carbocyclisation.” 2010. Web. 20 Jun 2019.

Vancouver:

Li M. Palladium catalysed allene carbocyclisation. [Internet] [Doctoral dissertation]. University of Oxford; 2010. [cited 2019 Jun 20]. Available from: http://ora.ox.ac.uk/objects/uuid:747420b6-c11f-451c-83c7-fa9fca5f7752 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543528.

Council of Science Editors:

Li M. Palladium catalysed allene carbocyclisation. [Doctoral Dissertation]. University of Oxford; 2010. Available from: http://ora.ox.ac.uk/objects/uuid:747420b6-c11f-451c-83c7-fa9fca5f7752 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.543528

21. Kolakowski, Robert Vincent, 1976-. New reactions, mechanisms, and stereochemical theory in organic chemistry.

Degree: PhD, Chemistry and Chemical Biology, 2010, Rutgers University

Here we describe a new method for the formation of allenes utilizing a Grob-like fragmentation along with a mechanistic study. The mechanism of the azide… (more)

Subjects/Keywords: Chemistry, Organic; Stereochemistry; Allene

…1 Chapter 1: Allene Synthesis via a Grob Like Fragmentation. Section 1.1: Allene… …therefore strategies for their application. The most useful stereoselective methods for allene… …led us to the develop a method of allene synthesis by C-C fragmentation. Olefin-formation… …6 1 (a) Hashmi, A. S. K., in Krause, N.; Hashmi, A. S. K. Modern Allene… …Hashmi, A. S. K. Modern Allene Chemistry, Vol. 2; Wiley-VCH Verlag: Weinhelm, 2004, pp 595-684… 

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APA (6th Edition):

Kolakowski, Robert Vincent, 1. (2010). New reactions, mechanisms, and stereochemical theory in organic chemistry. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056477

Chicago Manual of Style (16th Edition):

Kolakowski, Robert Vincent, 1976-. “New reactions, mechanisms, and stereochemical theory in organic chemistry.” 2010. Doctoral Dissertation, Rutgers University. Accessed June 20, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056477.

MLA Handbook (7th Edition):

Kolakowski, Robert Vincent, 1976-. “New reactions, mechanisms, and stereochemical theory in organic chemistry.” 2010. Web. 20 Jun 2019.

Vancouver:

Kolakowski, Robert Vincent 1. New reactions, mechanisms, and stereochemical theory in organic chemistry. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Jun 20]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056477.

Council of Science Editors:

Kolakowski, Robert Vincent 1. New reactions, mechanisms, and stereochemical theory in organic chemistry. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056477

22. Inghrim, Jennifer A., 1979-. 1. Nucleophilic addition to spirodiepoxides 2. Synthesis of psymberin analogues.

Degree: MS, Chemistry and Chemical Biology, 2011, Rutgers University

 The addition of nucleophiles to SDEs (SDEs), the double oxidation product of allenes, offers a concise and stereoselective method for the preparation of highly functionalized… (more)

Subjects/Keywords: Allene—Oxidation; Ketones

Allene Oxidation Model 11 Scheme 1.14 Diastereoselectivity of Allene Oxidation 13 Scheme… …Synthesis of Allene 1.102 23 ix Scheme 1.21 Stereoselective Model for Allene Oxidation 24… …x5B;Allene] 1.111 26 Scheme 1.24 Nucleophilic Opening of Bis-Allenes 27 Chapter 2… …Regioselectivity of Silyl Allene Oxidation 48 Scheme 3.4 DMDO Oxidation of Tetrasubstituted Silyl… …Allene 3.28 49 Scheme 3.5 Oxidation of a 1,1,3-Trisubstituted Silyl Allene 49 Scheme 3.6… 

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APA (6th Edition):

Inghrim, Jennifer A., 1. (2011). 1. Nucleophilic addition to spirodiepoxides 2. Synthesis of psymberin analogues. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063469

Chicago Manual of Style (16th Edition):

Inghrim, Jennifer A., 1979-. “1. Nucleophilic addition to spirodiepoxides 2. Synthesis of psymberin analogues.” 2011. Masters Thesis, Rutgers University. Accessed June 20, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063469.

MLA Handbook (7th Edition):

Inghrim, Jennifer A., 1979-. “1. Nucleophilic addition to spirodiepoxides 2. Synthesis of psymberin analogues.” 2011. Web. 20 Jun 2019.

Vancouver:

Inghrim, Jennifer A. 1. 1. Nucleophilic addition to spirodiepoxides 2. Synthesis of psymberin analogues. [Internet] [Masters thesis]. Rutgers University; 2011. [cited 2019 Jun 20]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063469.

Council of Science Editors:

Inghrim, Jennifer A. 1. 1. Nucleophilic addition to spirodiepoxides 2. Synthesis of psymberin analogues. [Masters Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063469


UCLA

23. Barber, Joyann. Harnessing the Reactivity of Strained Intermediates and Biosynthetic Machinery.

Degree: Chemistry, 2019, UCLA

 This dissertation describes efforts in strained allene and alkyne methodology, as well as collaborative efforts at the interface of organic synthesis and bioengineering to construct… (more)

Subjects/Keywords: Chemistry; Organic chemistry; allene methodology; organic synthesis; strained intermediates

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APA (6th Edition):

Barber, J. (2019). Harnessing the Reactivity of Strained Intermediates and Biosynthetic Machinery. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/3h61555b

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):

Barber, Joyann. “Harnessing the Reactivity of Strained Intermediates and Biosynthetic Machinery.” 2019. Thesis, UCLA. Accessed June 20, 2019. http://www.escholarship.org/uc/item/3h61555b.

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

MLA Handbook (7th Edition):

Barber, Joyann. “Harnessing the Reactivity of Strained Intermediates and Biosynthetic Machinery.” 2019. Web. 20 Jun 2019.

Vancouver:

Barber J. Harnessing the Reactivity of Strained Intermediates and Biosynthetic Machinery. [Internet] [Thesis]. UCLA; 2019. [cited 2019 Jun 20]. Available from: http://www.escholarship.org/uc/item/3h61555b.

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

Council of Science Editors:

Barber J. Harnessing the Reactivity of Strained Intermediates and Biosynthetic Machinery. [Thesis]. UCLA; 2019. Available from: http://www.escholarship.org/uc/item/3h61555b

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


Loughborough University

24. Al-Jawaheri, Yassir. An efficient synthesis of natural products using singlet oxygen.

Degree: PhD, 2019, Loughborough University

 The treatment of 1,3-dienes with singlet oxygen to give endoperoxides represents a potent, chemo- and regioselective method for the introduction of oxygen functionality. Additionally, these… (more)

Subjects/Keywords: Singlet oxygen; Endoperoxide; Allene; 1,3-diene; Moracin M; Resveratrol; Xanthanolides; Rearrangement

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APA (6th Edition):

Al-Jawaheri, Y. (2019). An efficient synthesis of natural products using singlet oxygen. (Doctoral Dissertation). Loughborough University. Retrieved from https://dspace.lboro.ac.uk/2134/36700 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771281

Chicago Manual of Style (16th Edition):

Al-Jawaheri, Yassir. “An efficient synthesis of natural products using singlet oxygen.” 2019. Doctoral Dissertation, Loughborough University. Accessed June 20, 2019. https://dspace.lboro.ac.uk/2134/36700 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771281.

MLA Handbook (7th Edition):

Al-Jawaheri, Yassir. “An efficient synthesis of natural products using singlet oxygen.” 2019. Web. 20 Jun 2019.

Vancouver:

Al-Jawaheri Y. An efficient synthesis of natural products using singlet oxygen. [Internet] [Doctoral dissertation]. Loughborough University; 2019. [cited 2019 Jun 20]. Available from: https://dspace.lboro.ac.uk/2134/36700 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771281.

Council of Science Editors:

Al-Jawaheri Y. An efficient synthesis of natural products using singlet oxygen. [Doctoral Dissertation]. Loughborough University; 2019. Available from: https://dspace.lboro.ac.uk/2134/36700 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771281


Johannes Gutenberg Universität Mainz

25. Perscheid, Moritz. Aufbau von 2-alkinyl-substituierten Azepanen und Piperidinen und deren Aza-Claisen-Umlagerungen zu Allenyllactamen.

Degree: 2010, Johannes Gutenberg Universität Mainz

Definiert konfigurierte mittelgroße ungesättigte Heterocyclen sind wertvolle Zwischenstufen in der Naturstoff- und Wirkstoffsynthese. Es konnte gezeigt werden, dass 2-alkinyl-substituierte Piperidine und Azepane in einer Aza-Keten-Claisen-Reaktion… (more)

Subjects/Keywords: Allene; Lactame; Claisen Umlagerung; Piperidine; Hetero-Diels-Alder-Reaktion; allenyl lactams; allene; Claisen rearrangement; piperidines; Hetero-Diels-Alder reaction; Chemistry and allied sciences

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APA (6th Edition):

Perscheid, M. (2010). Aufbau von 2-alkinyl-substituierten Azepanen und Piperidinen und deren Aza-Claisen-Umlagerungen zu Allenyllactamen. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2011/2770/

Chicago Manual of Style (16th Edition):

Perscheid, Moritz. “Aufbau von 2-alkinyl-substituierten Azepanen und Piperidinen und deren Aza-Claisen-Umlagerungen zu Allenyllactamen.” 2010. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed June 20, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2011/2770/.

MLA Handbook (7th Edition):

Perscheid, Moritz. “Aufbau von 2-alkinyl-substituierten Azepanen und Piperidinen und deren Aza-Claisen-Umlagerungen zu Allenyllactamen.” 2010. Web. 20 Jun 2019.

Vancouver:

Perscheid M. Aufbau von 2-alkinyl-substituierten Azepanen und Piperidinen und deren Aza-Claisen-Umlagerungen zu Allenyllactamen. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2010. [cited 2019 Jun 20]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2011/2770/.

Council of Science Editors:

Perscheid M. Aufbau von 2-alkinyl-substituierten Azepanen und Piperidinen und deren Aza-Claisen-Umlagerungen zu Allenyllactamen. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2010. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2011/2770/


The Ohio State University

26. Mans, Daniel J. Exocyclic Stereocontrol via Asymmetric Hydrovinylation in the General Synthesis of Pseudopterogorgia Natural Products Stereoselective X-Y-Mediated Cyclization Studies of an Allene-Ynamide and an Allene-Aldehyde.

Degree: PhD, Chemistry, 2008, The Ohio State University

  Asymmetric hydrovinylation, the heterodimerization of a prochiral olefin with ethylene gas, has been used to control the exocyclic stereochemistry in the construction of highly… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Pharmaceuticals; asymmetric hydrovinylation; exocyclic stereocontrol; green chemistry; ethylene in synthesis; methyl-bearing chiral centers; nickel catalysis; phosphoramidite ligands; NaBARF; allene-aldehyde cyclization; allene-ynamide cyclization

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

APA (6th Edition):

Mans, D. J. (2008). Exocyclic Stereocontrol via Asymmetric Hydrovinylation in the General Synthesis of Pseudopterogorgia Natural Products Stereoselective X-Y-Mediated Cyclization Studies of an Allene-Ynamide and an Allene-Aldehyde. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1203969383

Chicago Manual of Style (16th Edition):

Mans, Daniel J. “Exocyclic Stereocontrol via Asymmetric Hydrovinylation in the General Synthesis of Pseudopterogorgia Natural Products Stereoselective X-Y-Mediated Cyclization Studies of an Allene-Ynamide and an Allene-Aldehyde.” 2008. Doctoral Dissertation, The Ohio State University. Accessed June 20, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1203969383.

MLA Handbook (7th Edition):

Mans, Daniel J. “Exocyclic Stereocontrol via Asymmetric Hydrovinylation in the General Synthesis of Pseudopterogorgia Natural Products Stereoselective X-Y-Mediated Cyclization Studies of an Allene-Ynamide and an Allene-Aldehyde.” 2008. Web. 20 Jun 2019.

Vancouver:

Mans DJ. Exocyclic Stereocontrol via Asymmetric Hydrovinylation in the General Synthesis of Pseudopterogorgia Natural Products Stereoselective X-Y-Mediated Cyclization Studies of an Allene-Ynamide and an Allene-Aldehyde. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2019 Jun 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1203969383.

Council of Science Editors:

Mans DJ. Exocyclic Stereocontrol via Asymmetric Hydrovinylation in the General Synthesis of Pseudopterogorgia Natural Products Stereoselective X-Y-Mediated Cyclization Studies of an Allene-Ynamide and an Allene-Aldehyde. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1203969383


Temple University

27. Kulyk, Svitlana. PYRIDONE PHOTOCYCLOADDITION IN SYNTHESIS OF DIVERSE NATURAL AND UNNATURAL PRODUCTS.

Degree: PhD, 2014, Temple University

Chemistry

2-Pyridones are known to undergo a facile [4+4] photocycloaddition with themselves and other conjugated molecules. These transformations provide an access to complex molecular structures… (more)

Subjects/Keywords: Chemistry; Organic chemistry;

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APA (6th Edition):

Kulyk, S. (2014). PYRIDONE PHOTOCYCLOADDITION IN SYNTHESIS OF DIVERSE NATURAL AND UNNATURAL PRODUCTS. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,250995

Chicago Manual of Style (16th Edition):

Kulyk, Svitlana. “PYRIDONE PHOTOCYCLOADDITION IN SYNTHESIS OF DIVERSE NATURAL AND UNNATURAL PRODUCTS.” 2014. Doctoral Dissertation, Temple University. Accessed June 20, 2019. http://digital.library.temple.edu/u?/p245801coll10,250995.

MLA Handbook (7th Edition):

Kulyk, Svitlana. “PYRIDONE PHOTOCYCLOADDITION IN SYNTHESIS OF DIVERSE NATURAL AND UNNATURAL PRODUCTS.” 2014. Web. 20 Jun 2019.

Vancouver:

Kulyk S. PYRIDONE PHOTOCYCLOADDITION IN SYNTHESIS OF DIVERSE NATURAL AND UNNATURAL PRODUCTS. [Internet] [Doctoral dissertation]. Temple University; 2014. [cited 2019 Jun 20]. Available from: http://digital.library.temple.edu/u?/p245801coll10,250995.

Council of Science Editors:

Kulyk S. PYRIDONE PHOTOCYCLOADDITION IN SYNTHESIS OF DIVERSE NATURAL AND UNNATURAL PRODUCTS. [Doctoral Dissertation]. Temple University; 2014. Available from: http://digital.library.temple.edu/u?/p245801coll10,250995


Montana Tech

28. Squire, David J. Investigation of carbene/allene pathways.

Degree: MS, 1996, Montana Tech

Subjects/Keywords: Carbenes (Methylene compounds); Allene.; Chemical reactions.

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APA (6th Edition):

Squire, D. J. (1996). Investigation of carbene/allene pathways. (Masters Thesis). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/8299

Chicago Manual of Style (16th Edition):

Squire, David J. “Investigation of carbene/allene pathways.” 1996. Masters Thesis, Montana Tech. Accessed June 20, 2019. https://scholarworks.umt.edu/etd/8299.

MLA Handbook (7th Edition):

Squire, David J. “Investigation of carbene/allene pathways.” 1996. Web. 20 Jun 2019.

Vancouver:

Squire DJ. Investigation of carbene/allene pathways. [Internet] [Masters thesis]. Montana Tech; 1996. [cited 2019 Jun 20]. Available from: https://scholarworks.umt.edu/etd/8299.

Council of Science Editors:

Squire DJ. Investigation of carbene/allene pathways. [Masters Thesis]. Montana Tech; 1996. Available from: https://scholarworks.umt.edu/etd/8299


University of Illinois – Chicago

29. 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 June 20, 2019. 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. 20 Jun 2019.

Vancouver:

Li J. Tandem Metathesis-Based Natural Product Synthesis & Synthesis of Cyclopropenes and Their Rearrangements. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Jun 20]. 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

30. 松本, 知也. 含フッ素HWE試薬を用いる四置換オレフィンおよびアレニルエステル誘導体の合成研究.

Degree: 博士(薬科学), 2017, Tokushima University / 徳島大学

Subjects/Keywords: Horner-Wadsworth-Emmons reaction; Fluoroolefin; Allene; Stereoselective; Grignard reagent

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

APA (6th Edition):

松本, . (2017). 含フッ素HWE試薬を用いる四置換オレフィンおよびアレニルエステル誘導体の合成研究. (Thesis). Tokushima University / 徳島大学. Retrieved from http://repo.lib.tokushima-u.ac.jp/110931

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):

松本, 知也. “含フッ素HWE試薬を用いる四置換オレフィンおよびアレニルエステル誘導体の合成研究.” 2017. Thesis, Tokushima University / 徳島大学. Accessed June 20, 2019. http://repo.lib.tokushima-u.ac.jp/110931.

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

MLA Handbook (7th Edition):

松本, 知也. “含フッ素HWE試薬を用いる四置換オレフィンおよびアレニルエステル誘導体の合成研究.” 2017. Web. 20 Jun 2019.

Vancouver:

松本 . 含フッ素HWE試薬を用いる四置換オレフィンおよびアレニルエステル誘導体の合成研究. [Internet] [Thesis]. Tokushima University / 徳島大学; 2017. [cited 2019 Jun 20]. Available from: http://repo.lib.tokushima-u.ac.jp/110931.

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

Council of Science Editors:

松本 . 含フッ素HWE試薬を用いる四置換オレフィンおよびアレニルエステル誘導体の合成研究. [Thesis]. Tokushima University / 徳島大学; 2017. Available from: http://repo.lib.tokushima-u.ac.jp/110931

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

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