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You searched for subject:( dienophile). Showing records 1 – 5 of 5 total matches.

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University of Cambridge

1. GUO, ZIJIAN. Developing unstrained alkenes and alkynes for bioorthogonal chemistry.

Degree: PhD, University of Cambridge

 Bioorthogonal reactions, due to its excellent selectivity and time-efficiency, have emerged as a popular tool for protein and cell probing. Among all the bioorthogonal reactions,… (more)

Subjects/Keywords: IEDDA; Bioorthogonal chemistry; Unstrained dienophile; Protein modification

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APA (6th Edition):

GUO, Z. (n.d.). Developing unstrained alkenes and alkynes for bioorthogonal chemistry. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/289423

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

Chicago Manual of Style (16th Edition):

GUO, ZIJIAN. “Developing unstrained alkenes and alkynes for bioorthogonal chemistry.” Doctoral Dissertation, University of Cambridge. Accessed January 18, 2020. https://www.repository.cam.ac.uk/handle/1810/289423.

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

MLA Handbook (7th Edition):

GUO, ZIJIAN. “Developing unstrained alkenes and alkynes for bioorthogonal chemistry.” Web. 18 Jan 2020.

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

Vancouver:

GUO Z. Developing unstrained alkenes and alkynes for bioorthogonal chemistry. [Internet] [Doctoral dissertation]. University of Cambridge; [cited 2020 Jan 18]. Available from: https://www.repository.cam.ac.uk/handle/1810/289423.

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

Council of Science Editors:

GUO Z. Developing unstrained alkenes and alkynes for bioorthogonal chemistry. [Doctoral Dissertation]. University of Cambridge; Available from: https://www.repository.cam.ac.uk/handle/1810/289423

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


University of Central Florida

2. Shah, Saral. Solution Processible Aromatic Polyimides Via Diels Alder Precursor.

Degree: 2008, University of Central Florida

 Aromatic polyimides are interesting materials since they possess outstanding key properties such as thermoxidative stability, high mechanical strength, high modulus, excellent electrical properties, and superior… (more)

Subjects/Keywords: Aromatic; Polyimides; Saral; Chemistry; Diels Alder; Synthesis. Polymer; Diaminoanthracene; Diene; Dienophile; Chemistry

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APA (6th Edition):

Shah, S. (2008). Solution Processible Aromatic Polyimides Via Diels Alder Precursor. (Masters Thesis). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/3636

Chicago Manual of Style (16th Edition):

Shah, Saral. “Solution Processible Aromatic Polyimides Via Diels Alder Precursor.” 2008. Masters Thesis, University of Central Florida. Accessed January 18, 2020. https://stars.library.ucf.edu/etd/3636.

MLA Handbook (7th Edition):

Shah, Saral. “Solution Processible Aromatic Polyimides Via Diels Alder Precursor.” 2008. Web. 18 Jan 2020.

Vancouver:

Shah S. Solution Processible Aromatic Polyimides Via Diels Alder Precursor. [Internet] [Masters thesis]. University of Central Florida; 2008. [cited 2020 Jan 18]. Available from: https://stars.library.ucf.edu/etd/3636.

Council of Science Editors:

Shah S. Solution Processible Aromatic Polyimides Via Diels Alder Precursor. [Masters Thesis]. University of Central Florida; 2008. Available from: https://stars.library.ucf.edu/etd/3636

3. 大房, 俊行. アミノジエンおよび環状ジエノフィルを用いたDiels-Alder反応と天然物合成への適用 : Diels-Alder reaction using aminodienes and cyclic dienophiles, and its application to synthesis of natural products.

Degree: Chiba University / 千葉大学

研究科: 千葉大学大学院薬学研究院

修了年:2011年

学位:千大院医薬博甲第薬123号

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

Subjects/Keywords: Diels-Alder reaction; aminodiene; cyclic dienophile; Diels-Alder反応; アミノジエン; 環状ジエノフィル

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APA (6th Edition):

大房, . (n.d.). アミノジエンおよび環状ジエノフィルを用いたDiels-Alder反応と天然物合成への適用 : Diels-Alder reaction using aminodienes and cyclic dienophiles, and its application to synthesis of natural products. (Thesis). Chiba University / 千葉大学. Retrieved from http://opac.ll.chiba-u.jp/da/curator/900116536/

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

Chicago Manual of Style (16th Edition):

大房, 俊行. “アミノジエンおよび環状ジエノフィルを用いたDiels-Alder反応と天然物合成への適用 : Diels-Alder reaction using aminodienes and cyclic dienophiles, and its application to synthesis of natural products.” Thesis, Chiba University / 千葉大学. Accessed January 18, 2020. http://opac.ll.chiba-u.jp/da/curator/900116536/.

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

MLA Handbook (7th Edition):

大房, 俊行. “アミノジエンおよび環状ジエノフィルを用いたDiels-Alder反応と天然物合成への適用 : Diels-Alder reaction using aminodienes and cyclic dienophiles, and its application to synthesis of natural products.” Web. 18 Jan 2020.

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

Vancouver:

大房 . アミノジエンおよび環状ジエノフィルを用いたDiels-Alder反応と天然物合成への適用 : Diels-Alder reaction using aminodienes and cyclic dienophiles, and its application to synthesis of natural products. [Internet] [Thesis]. Chiba University / 千葉大学; [cited 2020 Jan 18]. Available from: http://opac.ll.chiba-u.jp/da/curator/900116536/.

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

Council of Science Editors:

大房 . アミノジエンおよび環状ジエノフィルを用いたDiels-Alder反応と天然物合成への適用 : Diels-Alder reaction using aminodienes and cyclic dienophiles, and its application to synthesis of natural products. [Thesis]. Chiba University / 千葉大学; Available from: http://opac.ll.chiba-u.jp/da/curator/900116536/

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

4. Newbury, Daniel John. Part A: Progress Towards the Total Synthesis of (±)-Communesin F; Part B: Aluminum as a Catalyst for the Diels-Alder Cycloaddition of Highly Hindered Dienophiles.

Degree: 2013, University of Ottawa

 This is a thesis in two parts. Part A examines two potential routes towards the synthesis of the communesin family of alkaloids, as well as… (more)

Subjects/Keywords: Total Synthesis; Diels-Alder; Communesin; Ethylaluminium Sesquichloride; Gold Catalysis; Hindered Dienophile

…50 Scheme 57: Preparation of highly hindered dienophile… …yield over two steps (Scheme 22). Scheme 22: Synthesis of the indole dienophile… 

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APA (6th Edition):

Newbury, D. J. (2013). Part A: Progress Towards the Total Synthesis of (±)-Communesin F; Part B: Aluminum as a Catalyst for the Diels-Alder Cycloaddition of Highly Hindered Dienophiles. (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/23943

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):

Newbury, Daniel John. “Part A: Progress Towards the Total Synthesis of (±)-Communesin F; Part B: Aluminum as a Catalyst for the Diels-Alder Cycloaddition of Highly Hindered Dienophiles. ” 2013. Thesis, University of Ottawa. Accessed January 18, 2020. http://hdl.handle.net/10393/23943.

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

MLA Handbook (7th Edition):

Newbury, Daniel John. “Part A: Progress Towards the Total Synthesis of (±)-Communesin F; Part B: Aluminum as a Catalyst for the Diels-Alder Cycloaddition of Highly Hindered Dienophiles. ” 2013. Web. 18 Jan 2020.

Vancouver:

Newbury DJ. Part A: Progress Towards the Total Synthesis of (±)-Communesin F; Part B: Aluminum as a Catalyst for the Diels-Alder Cycloaddition of Highly Hindered Dienophiles. [Internet] [Thesis]. University of Ottawa; 2013. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/10393/23943.

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

Council of Science Editors:

Newbury DJ. Part A: Progress Towards the Total Synthesis of (±)-Communesin F; Part B: Aluminum as a Catalyst for the Diels-Alder Cycloaddition of Highly Hindered Dienophiles. [Thesis]. University of Ottawa; 2013. Available from: http://hdl.handle.net/10393/23943

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


Université Paris-Sud – Paris XI

5. Sancibrao, Pierre. Cycloadditions de nitroso Diels-Alder asymétriques et régiosélectives : une nouvelle voie synthétique d'hétérospirocycles : Asymmetric and regioselective cycloadditions of nitroso Diels-Alder : a new synthetic route of heterospirocycles.

Degree: Docteur es, Chimie organique, 2012, Université Paris-Sud – Paris XI

Au cours de ce projet de recherche, nous nous sommes intéressés à la synthèse de motifs hétérospiraniques énantioenrichis. De ce fait, notre équipe a pu… (more)

Subjects/Keywords: Nitroso Diels-Alder; Cycloaddition; Spiroéther; Hétérospirobicycle; Diénophile dérivé de D-xylose; Pyridine nitroso; Rupture de liaison N-O; Réaction de Suzuki; Nitroso Diels-Alder; Cycloaddition; Spiroether; Heterospirobicycle; D-xylose derivative dienophile; Pyridine nitroso; N-O cleavage; Suzuki reaction

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APA (6th Edition):

Sancibrao, P. (2012). Cycloadditions de nitroso Diels-Alder asymétriques et régiosélectives : une nouvelle voie synthétique d'hétérospirocycles : Asymmetric and regioselective cycloadditions of nitroso Diels-Alder : a new synthetic route of heterospirocycles. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA112417

Chicago Manual of Style (16th Edition):

Sancibrao, Pierre. “Cycloadditions de nitroso Diels-Alder asymétriques et régiosélectives : une nouvelle voie synthétique d'hétérospirocycles : Asymmetric and regioselective cycloadditions of nitroso Diels-Alder : a new synthetic route of heterospirocycles.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 18, 2020. http://www.theses.fr/2012PA112417.

MLA Handbook (7th Edition):

Sancibrao, Pierre. “Cycloadditions de nitroso Diels-Alder asymétriques et régiosélectives : une nouvelle voie synthétique d'hétérospirocycles : Asymmetric and regioselective cycloadditions of nitroso Diels-Alder : a new synthetic route of heterospirocycles.” 2012. Web. 18 Jan 2020.

Vancouver:

Sancibrao P. Cycloadditions de nitroso Diels-Alder asymétriques et régiosélectives : une nouvelle voie synthétique d'hétérospirocycles : Asymmetric and regioselective cycloadditions of nitroso Diels-Alder : a new synthetic route of heterospirocycles. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2020 Jan 18]. Available from: http://www.theses.fr/2012PA112417.

Council of Science Editors:

Sancibrao P. Cycloadditions de nitroso Diels-Alder asymétriques et régiosélectives : une nouvelle voie synthétique d'hétérospirocycles : Asymmetric and regioselective cycloadditions of nitroso Diels-Alder : a new synthetic route of heterospirocycles. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA112417

.