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You searched for subject:(Diels Alder reactions). Showing records 1 – 30 of 42 total matches.

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UCLA

1. LIU, FANG. Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines.

Degree: Chemistry, 2014, UCLA

 The concept of gating was introduced into host-guest chemistry by our group in the 1990s, as a result of computational studies on Cram's hemicarcerands. Since… (more)

Subjects/Keywords: Chemistry; Diels-Alder reactions; Gating; Hemicarcerands; Tetrazines

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APA (6th Edition):

LIU, F. (2014). Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6028d3n8

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):

LIU, FANG. “Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines.” 2014. Thesis, UCLA. Accessed September 17, 2019. http://www.escholarship.org/uc/item/6028d3n8.

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

MLA Handbook (7th Edition):

LIU, FANG. “Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines.” 2014. Web. 17 Sep 2019.

Vancouver:

LIU F. Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines. [Internet] [Thesis]. UCLA; 2014. [cited 2019 Sep 17]. Available from: http://www.escholarship.org/uc/item/6028d3n8.

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

Council of Science Editors:

LIU F. Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/6028d3n8

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


Australian National University

2. Saglam, Mehmet Fatih. Investigation into Higher Dendralenes .

Degree: 2016, Australian National University

 As synthetic organic chemists, one of our most important desires is to synthesize complex target molecules efficiently in the shortest time and lowest step count,… (more)

Subjects/Keywords: Hydrocarbons; Dendralenes; Diels-Alder reactions; Metal Catalysed Cross-Coupling reactions

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APA (6th Edition):

Saglam, M. F. (2016). Investigation into Higher Dendralenes . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/107105

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):

Saglam, Mehmet Fatih. “Investigation into Higher Dendralenes .” 2016. Thesis, Australian National University. Accessed September 17, 2019. http://hdl.handle.net/1885/107105.

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

MLA Handbook (7th Edition):

Saglam, Mehmet Fatih. “Investigation into Higher Dendralenes .” 2016. Web. 17 Sep 2019.

Vancouver:

Saglam MF. Investigation into Higher Dendralenes . [Internet] [Thesis]. Australian National University; 2016. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/1885/107105.

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

Council of Science Editors:

Saglam MF. Investigation into Higher Dendralenes . [Thesis]. Australian National University; 2016. Available from: http://hdl.handle.net/1885/107105

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


University of Alberta

3. Han, Yongxin. S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones.

Degree: PhD, Department of Chemistry, 1992, University of Alberta

Subjects/Keywords: Diels-Alder reaction.; Chemical reactions.

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APA (6th Edition):

Han, Y. (1992). S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cr56n283p

Chicago Manual of Style (16th Edition):

Han, Yongxin. “S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones.” 1992. Doctoral Dissertation, University of Alberta. Accessed September 17, 2019. https://era.library.ualberta.ca/files/cr56n283p.

MLA Handbook (7th Edition):

Han, Yongxin. “S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones.” 1992. Web. 17 Sep 2019.

Vancouver:

Han Y. S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones. [Internet] [Doctoral dissertation]. University of Alberta; 1992. [cited 2019 Sep 17]. Available from: https://era.library.ualberta.ca/files/cr56n283p.

Council of Science Editors:

Han Y. S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones. [Doctoral Dissertation]. University of Alberta; 1992. Available from: https://era.library.ualberta.ca/files/cr56n283p


Miami University

4. Deng, Yongming. Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins.

Degree: PhD, Chemistry, 2014, Miami University

 The combination of enamine catalysis with metal catalysis, aiming to achieve organic transformations that cannot be accessed by enamine catalysis or metal catalysis independently, promises… (more)

Subjects/Keywords: Chemistry; cooperative catalysis; enamines; Lewis acids; multicomponent reactions; aza-Diels-Alder reactions

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APA (6th Edition):

Deng, Y. (2014). Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins. (Doctoral Dissertation). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1406213121

Chicago Manual of Style (16th Edition):

Deng, Yongming. “Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins.” 2014. Doctoral Dissertation, Miami University. Accessed September 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=miami1406213121.

MLA Handbook (7th Edition):

Deng, Yongming. “Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins.” 2014. Web. 17 Sep 2019.

Vancouver:

Deng Y. Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins. [Internet] [Doctoral dissertation]. Miami University; 2014. [cited 2019 Sep 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1406213121.

Council of Science Editors:

Deng Y. Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins. [Doctoral Dissertation]. Miami University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1406213121


Australian National University

5. Joshua William, Boyle. A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis .

Degree: 2015, Australian National University

 [3]Dendralene is a small π-­rich hydrocarbon that is capable of taking part in a wide range of chemical reactions, not least of which is the… (more)

Subjects/Keywords: Diels-Alder; DTDA; Total Synthesis; Methodology; Domino reactions; Cross-coupling reactions; xestoquinone

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APA (6th Edition):

Joshua William, B. (2015). A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/101992

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):

Joshua William, Boyle. “A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis .” 2015. Thesis, Australian National University. Accessed September 17, 2019. http://hdl.handle.net/1885/101992.

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

MLA Handbook (7th Edition):

Joshua William, Boyle. “A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis .” 2015. Web. 17 Sep 2019.

Vancouver:

Joshua William B. A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis . [Internet] [Thesis]. Australian National University; 2015. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/1885/101992.

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

Council of Science Editors:

Joshua William B. A Unified Approach to Carbocyclic Frameworks: DTDA Sequences in Total Synthesis . [Thesis]. Australian National University; 2015. Available from: http://hdl.handle.net/1885/101992

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


University of Otago

6. Moodie, Lindon William Kirk. An Enyne Metathesis Approach to the Angucycline Natural Products .

Degree: 2013, University of Otago

 The research in this thesis aimed to identify a common intermediate that would allow the collective synthesis of structurally diverse members of the angucycline antibiotics… (more)

Subjects/Keywords: Organic Chemistry; Natural Products; Total Synthesis; Angucyclines; Tetrangomycin; Enyne Metathesis; Tandem Reactions; Diels Alder

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APA (6th Edition):

Moodie, L. W. K. (2013). An Enyne Metathesis Approach to the Angucycline Natural Products . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/4063

Chicago Manual of Style (16th Edition):

Moodie, Lindon William Kirk. “An Enyne Metathesis Approach to the Angucycline Natural Products .” 2013. Doctoral Dissertation, University of Otago. Accessed September 17, 2019. http://hdl.handle.net/10523/4063.

MLA Handbook (7th Edition):

Moodie, Lindon William Kirk. “An Enyne Metathesis Approach to the Angucycline Natural Products .” 2013. Web. 17 Sep 2019.

Vancouver:

Moodie LWK. An Enyne Metathesis Approach to the Angucycline Natural Products . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10523/4063.

Council of Science Editors:

Moodie LWK. An Enyne Metathesis Approach to the Angucycline Natural Products . [Doctoral Dissertation]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4063


University of Alberta

7. Wingert, David Alexander. Indolizidine alkaloids and asymmetric synthesis of carbocycles.

Degree: PhD, Department of Chemistry, 2012, University of Alberta

 The first chapter of this thesis describes the development of an asymmetric route to the core structure of the indolizidine alkaloids and its application to… (more)

Subjects/Keywords: indolizidine; ntramolecular conjugate displacement reactions (ICD); Diels-Alder reactions; (+)-ipalbidine; assymmetric synthesis; Myers asymmetric alkylation; conjugate additions; asymmetric carbocycle synthesis

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APA (6th Edition):

Wingert, D. A. (2012). Indolizidine alkaloids and asymmetric synthesis of carbocycles. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/0z708w967

Chicago Manual of Style (16th Edition):

Wingert, David Alexander. “Indolizidine alkaloids and asymmetric synthesis of carbocycles.” 2012. Doctoral Dissertation, University of Alberta. Accessed September 17, 2019. https://era.library.ualberta.ca/files/0z708w967.

MLA Handbook (7th Edition):

Wingert, David Alexander. “Indolizidine alkaloids and asymmetric synthesis of carbocycles.” 2012. Web. 17 Sep 2019.

Vancouver:

Wingert DA. Indolizidine alkaloids and asymmetric synthesis of carbocycles. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2019 Sep 17]. Available from: https://era.library.ualberta.ca/files/0z708w967.

Council of Science Editors:

Wingert DA. Indolizidine alkaloids and asymmetric synthesis of carbocycles. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/0z708w967

8. Cardoso Filho, José Eduardo Pandini. Estudos de diastereosseletividade facial em reações de Diels-Alder de sulfinil benzoquinonas e em adições nucleofílicas a sulfinil cicloexanonas sulfaniladas.

Degree: PhD, Química Orgânica, 2008, University of São Paulo

Calcando-se na bem conhecida capacidade que os sulfóxidos apresentam em induzir a quiralidade em uma vasta gama de reações, foram preparadas as (±)-2-p-tolilsulfinil-3,6-dimetil- e a… (more)

Subjects/Keywords: Benzoquinona; Benzoquinone; Cicloexanona; Compostos de enxofre; Cyclohexanone; Diels-Alder; Diels-Alder; Facial selectivity; Organic reactions; Organic synthesis; Reações químicas; Seletividade facial; Síntese orgânica; Sulfoxide; Sulfóxido

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APA (6th Edition):

Cardoso Filho, J. E. P. (2008). Estudos de diastereosseletividade facial em reações de Diels-Alder de sulfinil benzoquinonas e em adições nucleofílicas a sulfinil cicloexanonas sulfaniladas. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-19122008-114737/ ;

Chicago Manual of Style (16th Edition):

Cardoso Filho, José Eduardo Pandini. “Estudos de diastereosseletividade facial em reações de Diels-Alder de sulfinil benzoquinonas e em adições nucleofílicas a sulfinil cicloexanonas sulfaniladas.” 2008. Doctoral Dissertation, University of São Paulo. Accessed September 17, 2019. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-19122008-114737/ ;.

MLA Handbook (7th Edition):

Cardoso Filho, José Eduardo Pandini. “Estudos de diastereosseletividade facial em reações de Diels-Alder de sulfinil benzoquinonas e em adições nucleofílicas a sulfinil cicloexanonas sulfaniladas.” 2008. Web. 17 Sep 2019.

Vancouver:

Cardoso Filho JEP. Estudos de diastereosseletividade facial em reações de Diels-Alder de sulfinil benzoquinonas e em adições nucleofílicas a sulfinil cicloexanonas sulfaniladas. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2019 Sep 17]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-19122008-114737/ ;.

Council of Science Editors:

Cardoso Filho JEP. Estudos de diastereosseletividade facial em reações de Diels-Alder de sulfinil benzoquinonas e em adições nucleofílicas a sulfinil cicloexanonas sulfaniladas. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-19122008-114737/ ;

9. Αρκούδης, Ηλίας. Βιομιμητική συνθετική προσέγγιση των φυσικών προϊόντων cordiaquinones, acremines και microphyllones.

Degree: 2009, University of Crete (UOC); Πανεπιστήμιο Κρήτης

In the present Ph. D. Thesis, the biomimetic synthesis of the natural products cordiaquinones B, C, J & K, acremines C & G and allomicrophyllone… (more)

Subjects/Keywords: Ζεόλιθος NaY; Εποξυτερπένια; Κυκλοποίηση; Φυσικά προϊόντα; Βιομιμητική σύνθεση; Αντίδραση Diels-Alder; Εκλεκτικότητα; Οξύ Lewis; Ζeolite NaY; Epoxy terpenes; Cyclization; Natural products; Biomimetic synthesis; Diels-Alder reactions; Lewis acid

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APA (6th Edition):

Αρκούδης, . . (2009). Βιομιμητική συνθετική προσέγγιση των φυσικών προϊόντων cordiaquinones, acremines και microphyllones. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/18755

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):

Αρκούδης, Ηλίας. “Βιομιμητική συνθετική προσέγγιση των φυσικών προϊόντων cordiaquinones, acremines και microphyllones.” 2009. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed September 17, 2019. http://hdl.handle.net/10442/hedi/18755.

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

MLA Handbook (7th Edition):

Αρκούδης, Ηλίας. “Βιομιμητική συνθετική προσέγγιση των φυσικών προϊόντων cordiaquinones, acremines και microphyllones.” 2009. Web. 17 Sep 2019.

Vancouver:

Αρκούδης . Βιομιμητική συνθετική προσέγγιση των φυσικών προϊόντων cordiaquinones, acremines και microphyllones. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2009. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10442/hedi/18755.

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

Council of Science Editors:

Αρκούδης . Βιομιμητική συνθετική προσέγγιση των φυσικών προϊόντων cordiaquinones, acremines και microphyllones. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2009. Available from: http://hdl.handle.net/10442/hedi/18755

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

10. Borne, Mathilde. Modifications chimiques, mécanismes de structuration et propriétés des matériaux à base de gluten : Chemical modifications, structuration mechanisms and properties of gluten-based materials.

Degree: Docteur es, Chimie des matériaux, 2012, Montpellier, Ecole nationale supérieure de chimie

Les matériaux agroressourcés à base de gluten de blé présentent des propriétés mécaniques qui ne leurs permettent pas de concurrencer celles des plastiques usuels issus… (more)

Subjects/Keywords: Gluten de blé; Agromatériaux; Diels-Alder; Maléimides; Réactions d'échandes thiols/disulfures; Feuillets-β; Wheat gluten; Bio-based materials; Diels-Alder; Maleimide; Exchange reactions thiol/disulfide; Β-sheets

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APA (6th Edition):

Borne, M. (2012). Modifications chimiques, mécanismes de structuration et propriétés des matériaux à base de gluten : Chemical modifications, structuration mechanisms and properties of gluten-based materials. (Doctoral Dissertation). Montpellier, Ecole nationale supérieure de chimie. Retrieved from http://www.theses.fr/2012ENCM0020

Chicago Manual of Style (16th Edition):

Borne, Mathilde. “Modifications chimiques, mécanismes de structuration et propriétés des matériaux à base de gluten : Chemical modifications, structuration mechanisms and properties of gluten-based materials.” 2012. Doctoral Dissertation, Montpellier, Ecole nationale supérieure de chimie. Accessed September 17, 2019. http://www.theses.fr/2012ENCM0020.

MLA Handbook (7th Edition):

Borne, Mathilde. “Modifications chimiques, mécanismes de structuration et propriétés des matériaux à base de gluten : Chemical modifications, structuration mechanisms and properties of gluten-based materials.” 2012. Web. 17 Sep 2019.

Vancouver:

Borne M. Modifications chimiques, mécanismes de structuration et propriétés des matériaux à base de gluten : Chemical modifications, structuration mechanisms and properties of gluten-based materials. [Internet] [Doctoral dissertation]. Montpellier, Ecole nationale supérieure de chimie; 2012. [cited 2019 Sep 17]. Available from: http://www.theses.fr/2012ENCM0020.

Council of Science Editors:

Borne M. Modifications chimiques, mécanismes de structuration et propriétés des matériaux à base de gluten : Chemical modifications, structuration mechanisms and properties of gluten-based materials. [Doctoral Dissertation]. Montpellier, Ecole nationale supérieure de chimie; 2012. Available from: http://www.theses.fr/2012ENCM0020

11. ΣΤΕΦΑΝΙΔΗΣ, ΙΩΑΝΝΗΣ. ΜΕΘΟΔΟΣ ΣΥΝΘΕΣΗΣ Η/ΚΑΙ ΕΠΙΛΟΓΗΣ  ΑΡΙΣΤΩΝ ΔΙΑΛΥΤΩΝ ΠΡΟΣ ΕΠΙΤΑΧΥΝΣΗ ΑΝΤΙΔΡΑΣΕΩΝ DIELS-ALDER.

Degree: 1986, Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ); National Technical University of Athens (NTUA)

ΜΕ ΒΑΣΗ ΜΙΑ ΣΧΕΣΗ ΜΕΤΑΞΥ ΤΟΥ ΡΥΘΜΟΥ ΑΝΤΙΔΡΑΣΕΩΝ ΚΑΙ ΣΥΝΤΕΛΕΣΤΩΝ ΕΝΕΡΓΟΤΗΤΑΣ (Γ) ΚΑΙ, ΜΙΑΣ ΜΕΘΟΔΟΥ ΥΠΟΛΟΓΙΣΜΟΥ ΣΥΝΤΕΛΕΣΤΩΝ ΕΝΕΡΓΟΤΗΤΑΣ (ΤΗΣ UNIFAC), ΜΕΛΕΤΗΘΗΚΕ Η ΕΠΙΔΡΑΣΗ ΔΙΑΦΟΡΩΝ ΔΙΑΛΥΤΩΝ… (more)

Subjects/Keywords: ΑΝΤΙΔΡΑΣΕΙΣ DIELS-ALDER Υ DIELS-ALDER REACTIONS LIQUID PHASE; ΕΠΙΤΑΧΥΝΣΗ ΑΝΤΙΔΡΑΣΕΩΝ DIELS-ALDER ΜΕ ΔΙΑΛΥΤΕΣ

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APA (6th Edition):

ΣΤΕΦΑΝΙΔΗΣ, . (1986). ΜΕΘΟΔΟΣ ΣΥΝΘΕΣΗΣ Η/ΚΑΙ ΕΠΙΛΟΓΗΣ  ΑΡΙΣΤΩΝ ΔΙΑΛΥΤΩΝ ΠΡΟΣ ΕΠΙΤΑΧΥΝΣΗ ΑΝΤΙΔΡΑΣΕΩΝ DIELS-ALDER. (Thesis). Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ); National Technical University of Athens (NTUA). Retrieved from http://hdl.handle.net/10442/hedi/0298

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):

ΣΤΕΦΑΝΙΔΗΣ, ΙΩΑΝΝΗΣ. “ΜΕΘΟΔΟΣ ΣΥΝΘΕΣΗΣ Η/ΚΑΙ ΕΠΙΛΟΓΗΣ  ΑΡΙΣΤΩΝ ΔΙΑΛΥΤΩΝ ΠΡΟΣ ΕΠΙΤΑΧΥΝΣΗ ΑΝΤΙΔΡΑΣΕΩΝ DIELS-ALDER.” 1986. Thesis, Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ); National Technical University of Athens (NTUA). Accessed September 17, 2019. http://hdl.handle.net/10442/hedi/0298.

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

MLA Handbook (7th Edition):

ΣΤΕΦΑΝΙΔΗΣ, ΙΩΑΝΝΗΣ. “ΜΕΘΟΔΟΣ ΣΥΝΘΕΣΗΣ Η/ΚΑΙ ΕΠΙΛΟΓΗΣ  ΑΡΙΣΤΩΝ ΔΙΑΛΥΤΩΝ ΠΡΟΣ ΕΠΙΤΑΧΥΝΣΗ ΑΝΤΙΔΡΑΣΕΩΝ DIELS-ALDER.” 1986. Web. 17 Sep 2019.

Vancouver:

ΣΤΕΦΑΝΙΔΗΣ . ΜΕΘΟΔΟΣ ΣΥΝΘΕΣΗΣ Η/ΚΑΙ ΕΠΙΛΟΓΗΣ  ΑΡΙΣΤΩΝ ΔΙΑΛΥΤΩΝ ΠΡΟΣ ΕΠΙΤΑΧΥΝΣΗ ΑΝΤΙΔΡΑΣΕΩΝ DIELS-ALDER. [Internet] [Thesis]. Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ); National Technical University of Athens (NTUA); 1986. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10442/hedi/0298.

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

Council of Science Editors:

ΣΤΕΦΑΝΙΔΗΣ . ΜΕΘΟΔΟΣ ΣΥΝΘΕΣΗΣ Η/ΚΑΙ ΕΠΙΛΟΓΗΣ  ΑΡΙΣΤΩΝ ΔΙΑΛΥΤΩΝ ΠΡΟΣ ΕΠΙΤΑΧΥΝΣΗ ΑΝΤΙΔΡΑΣΕΩΝ DIELS-ALDER. [Thesis]. Εθνικό Μετσόβιο Πολυτεχνείο (ΕΜΠ); National Technical University of Athens (NTUA); 1986. Available from: http://hdl.handle.net/10442/hedi/0298

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


University of KwaZulu-Natal

12. [No author]. The use of ephedrine and camphor in asymmetric Diels-Alder reactions.

Degree: Chemistry, 1997, University of KwaZulu-Natal

 Due to the ever increasing demand for the production of enantiopure drugs and biologically active compounds, the study of asymmetric synthesis and the production of… (more)

Subjects/Keywords: Stereochemistry.; Diels-Alder Reaction.; Chemical reactions.; Chemistry.

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APA (6th Edition):

author], [. (1997). The use of ephedrine and camphor in asymmetric Diels-Alder reactions. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/6001

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):

author], [No. “The use of ephedrine and camphor in asymmetric Diels-Alder reactions. ” 1997. Thesis, University of KwaZulu-Natal. Accessed September 17, 2019. http://hdl.handle.net/10413/6001.

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

MLA Handbook (7th Edition):

author], [No. “The use of ephedrine and camphor in asymmetric Diels-Alder reactions. ” 1997. Web. 17 Sep 2019.

Vancouver:

author] [. The use of ephedrine and camphor in asymmetric Diels-Alder reactions. [Internet] [Thesis]. University of KwaZulu-Natal; 1997. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10413/6001.

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

Council of Science Editors:

author] [. The use of ephedrine and camphor in asymmetric Diels-Alder reactions. [Thesis]. University of KwaZulu-Natal; 1997. Available from: http://hdl.handle.net/10413/6001

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


Montana State University

13. Link, Jeffrey Stevens. Novel synthetic methodologies : radical and photochemical approaches towards alkaloids. Diels-Alder methodology towards inositol derivatives.

Degree: College of Letters & Science, 2000, Montana State University

Subjects/Keywords: Ring formation (Chemistry); Free radical reactions.; Diels-Alder reaction.

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APA (6th Edition):

Link, J. S. (2000). Novel synthetic methodologies : radical and photochemical approaches towards alkaloids. Diels-Alder methodology towards inositol derivatives. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/8050

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):

Link, Jeffrey Stevens. “Novel synthetic methodologies : radical and photochemical approaches towards alkaloids. Diels-Alder methodology towards inositol derivatives.” 2000. Thesis, Montana State University. Accessed September 17, 2019. https://scholarworks.montana.edu/xmlui/handle/1/8050.

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

MLA Handbook (7th Edition):

Link, Jeffrey Stevens. “Novel synthetic methodologies : radical and photochemical approaches towards alkaloids. Diels-Alder methodology towards inositol derivatives.” 2000. Web. 17 Sep 2019.

Vancouver:

Link JS. Novel synthetic methodologies : radical and photochemical approaches towards alkaloids. Diels-Alder methodology towards inositol derivatives. [Internet] [Thesis]. Montana State University; 2000. [cited 2019 Sep 17]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/8050.

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

Council of Science Editors:

Link JS. Novel synthetic methodologies : radical and photochemical approaches towards alkaloids. Diels-Alder methodology towards inositol derivatives. [Thesis]. Montana State University; 2000. Available from: https://scholarworks.montana.edu/xmlui/handle/1/8050

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


University of North Carolina – Wilmington

14. MacNevin, Christopher J. Reactivity of substituted 4-Pyridones in normal and inverse demand Diels-Alder cycloaddition.

Degree: 2009, University of North Carolina – Wilmington

 The synthesis of the decahydroquinoline ring system has been explored extensively due to its appearance within many biologically active natural alkaloids. New compounds containing such… (more)

Subjects/Keywords: Diels-Alder reaction; Ring formation (Chemistry); Diolefins; Chemical reactions

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APA (6th Edition):

MacNevin, C. J. (2009). Reactivity of substituted 4-Pyridones in normal and inverse demand Diels-Alder cycloaddition. (Masters Thesis). University of North Carolina – Wilmington. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=857

Chicago Manual of Style (16th Edition):

MacNevin, Christopher J. “Reactivity of substituted 4-Pyridones in normal and inverse demand Diels-Alder cycloaddition.” 2009. Masters Thesis, University of North Carolina – Wilmington. Accessed September 17, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=857.

MLA Handbook (7th Edition):

MacNevin, Christopher J. “Reactivity of substituted 4-Pyridones in normal and inverse demand Diels-Alder cycloaddition.” 2009. Web. 17 Sep 2019.

Vancouver:

MacNevin CJ. Reactivity of substituted 4-Pyridones in normal and inverse demand Diels-Alder cycloaddition. [Internet] [Masters thesis]. University of North Carolina – Wilmington; 2009. [cited 2019 Sep 17]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=857.

Council of Science Editors:

MacNevin CJ. Reactivity of substituted 4-Pyridones in normal and inverse demand Diels-Alder cycloaddition. [Masters Thesis]. University of North Carolina – Wilmington; 2009. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=857


University of Central Florida

15. Johns, Valentine. Photochemistry And Applications Of Diels-alder Adducts And Photoacids In Materials Science.

Degree: 2012, University of Central Florida

 In chapter I Photo-retro-Diels-Alder (PrDA) reactions of a variety of Diels Alder (DA) adducts were studied. Experimental results showed that the photoreactivity (quantum yield) depends… (more)

Subjects/Keywords: Photochemistry; photo retro diels alder reactions; photoacid; pentacene; polymers; materials; Chemistry; Dissertations, Academic  – Sciences, Sciences  – Dissertations, Academic

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APA (6th Edition):

Johns, V. (2012). Photochemistry And Applications Of Diels-alder Adducts And Photoacids In Materials Science. (Doctoral Dissertation). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/2496

Chicago Manual of Style (16th Edition):

Johns, Valentine. “Photochemistry And Applications Of Diels-alder Adducts And Photoacids In Materials Science.” 2012. Doctoral Dissertation, University of Central Florida. Accessed September 17, 2019. https://stars.library.ucf.edu/etd/2496.

MLA Handbook (7th Edition):

Johns, Valentine. “Photochemistry And Applications Of Diels-alder Adducts And Photoacids In Materials Science.” 2012. Web. 17 Sep 2019.

Vancouver:

Johns V. Photochemistry And Applications Of Diels-alder Adducts And Photoacids In Materials Science. [Internet] [Doctoral dissertation]. University of Central Florida; 2012. [cited 2019 Sep 17]. Available from: https://stars.library.ucf.edu/etd/2496.

Council of Science Editors:

Johns V. Photochemistry And Applications Of Diels-alder Adducts And Photoacids In Materials Science. [Doctoral Dissertation]. University of Central Florida; 2012. Available from: https://stars.library.ucf.edu/etd/2496


University of North Texas

16. Dong, Zhiming (Eric). New Adventures in the Chemistry of Polycarboncyclic Ring Systems.

Degree: 1997, University of North Texas

 I. Diels-Alder reactions of 1,2,3,4,9,9-hexachloro-1,4,4a,8a-tetrahydro-1,4-metha- nonaphthalene (16) and 1,2,3,4,9,9-hexachloro-1,4,6,7-tetrahydro-1,4-methanonaphthalene (17) toward dienophiles N-methyl-1,2,4-triazoline-3,5-dione (MTAD), N-phenyl-1,2,4-triazoline-3,5-dione (PTAD) and/or N-methylmaleimide (NMM) have been examined. II. Epoxides derived… (more)

Subjects/Keywords: Diels-Alder reactions; epoxides; chemistry; Polycyclic compounds.

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APA (6th Edition):

Dong, Z. (. (1997). New Adventures in the Chemistry of Polycarboncyclic Ring Systems. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc278356/

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):

Dong, Zhiming (Eric). “New Adventures in the Chemistry of Polycarboncyclic Ring Systems.” 1997. Thesis, University of North Texas. Accessed September 17, 2019. https://digital.library.unt.edu/ark:/67531/metadc278356/.

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

MLA Handbook (7th Edition):

Dong, Zhiming (Eric). “New Adventures in the Chemistry of Polycarboncyclic Ring Systems.” 1997. Web. 17 Sep 2019.

Vancouver:

Dong Z(. New Adventures in the Chemistry of Polycarboncyclic Ring Systems. [Internet] [Thesis]. University of North Texas; 1997. [cited 2019 Sep 17]. Available from: https://digital.library.unt.edu/ark:/67531/metadc278356/.

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

Council of Science Editors:

Dong Z(. New Adventures in the Chemistry of Polycarboncyclic Ring Systems. [Thesis]. University of North Texas; 1997. Available from: https://digital.library.unt.edu/ark:/67531/metadc278356/

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


Michigan State University

17. Peng, Cheng-Tai, 1943-. Part I: Synthesis and photochemistry of cyclohexadienone epoxides.

Degree: PhD, 1977, Michigan State University

Subjects/Keywords: Epoxy compounds; Diels-Alder reaction; Chemical reactions; Chemistry, Organic

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APA (6th Edition):

Peng, Cheng-Tai, 1. (1977). Part I: Synthesis and photochemistry of cyclohexadienone epoxides. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:35095

Chicago Manual of Style (16th Edition):

Peng, Cheng-Tai, 1943-. “Part I: Synthesis and photochemistry of cyclohexadienone epoxides.” 1977. Doctoral Dissertation, Michigan State University. Accessed September 17, 2019. http://etd.lib.msu.edu/islandora/object/etd:35095.

MLA Handbook (7th Edition):

Peng, Cheng-Tai, 1943-. “Part I: Synthesis and photochemistry of cyclohexadienone epoxides.” 1977. Web. 17 Sep 2019.

Vancouver:

Peng, Cheng-Tai 1. Part I: Synthesis and photochemistry of cyclohexadienone epoxides. [Internet] [Doctoral dissertation]. Michigan State University; 1977. [cited 2019 Sep 17]. Available from: http://etd.lib.msu.edu/islandora/object/etd:35095.

Council of Science Editors:

Peng, Cheng-Tai 1. Part I: Synthesis and photochemistry of cyclohexadienone epoxides. [Doctoral Dissertation]. Michigan State University; 1977. Available from: http://etd.lib.msu.edu/islandora/object/etd:35095


Michigan State University

18. Newman, Cory Allan. Catalytic asymmetric aza-Diels-Alder reaction : regulation of orthogonal functions in a duel chiral/non-chiral catalyst system.

Degree: PhD, Department of Chemistry, 2007, Michigan State University

Subjects/Keywords: Diels-Alder reaction; Asymmetry (Chemistry); Enantioselective catalysis; Chemical reactions

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APA (6th Edition):

Newman, C. A. (2007). Catalytic asymmetric aza-Diels-Alder reaction : regulation of orthogonal functions in a duel chiral/non-chiral catalyst system. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:38485

Chicago Manual of Style (16th Edition):

Newman, Cory Allan. “Catalytic asymmetric aza-Diels-Alder reaction : regulation of orthogonal functions in a duel chiral/non-chiral catalyst system.” 2007. Doctoral Dissertation, Michigan State University. Accessed September 17, 2019. http://etd.lib.msu.edu/islandora/object/etd:38485.

MLA Handbook (7th Edition):

Newman, Cory Allan. “Catalytic asymmetric aza-Diels-Alder reaction : regulation of orthogonal functions in a duel chiral/non-chiral catalyst system.” 2007. Web. 17 Sep 2019.

Vancouver:

Newman CA. Catalytic asymmetric aza-Diels-Alder reaction : regulation of orthogonal functions in a duel chiral/non-chiral catalyst system. [Internet] [Doctoral dissertation]. Michigan State University; 2007. [cited 2019 Sep 17]. Available from: http://etd.lib.msu.edu/islandora/object/etd:38485.

Council of Science Editors:

Newman CA. Catalytic asymmetric aza-Diels-Alder reaction : regulation of orthogonal functions in a duel chiral/non-chiral catalyst system. [Doctoral Dissertation]. Michigan State University; 2007. Available from: http://etd.lib.msu.edu/islandora/object/etd:38485

19. Jomon Jacob, P. Ground and Excited State Electron Transfer Reaction Between a few Anthracene Appended Tertiary Amines and Suitable Electron Acceptors.

Degree: 2013, Cochin University of Science and Technology

the thesis entitled “Ground and Excited State Electron Transfer Reaction Between a few Anthracene Appended Tertiary Amines and Suitable Electron Acceptors” portrays our attempts to… (more)

Subjects/Keywords: Electron Transfer Reactions; Electron Transfer Reactions of Amines; Michael Addition Reactions; Diels-Alder Reaction; Synthesis And Characterisation Of A Few (Anthracen-9-Yl)Methanamines

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APA (6th Edition):

Jomon Jacob, P. (2013). Ground and Excited State Electron Transfer Reaction Between a few Anthracene Appended Tertiary Amines and Suitable Electron Acceptors. (Thesis). Cochin University of Science and Technology. Retrieved from http://dyuthi.cusat.ac.in/purl/4625

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):

Jomon Jacob, P. “Ground and Excited State Electron Transfer Reaction Between a few Anthracene Appended Tertiary Amines and Suitable Electron Acceptors.” 2013. Thesis, Cochin University of Science and Technology. Accessed September 17, 2019. http://dyuthi.cusat.ac.in/purl/4625.

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

MLA Handbook (7th Edition):

Jomon Jacob, P. “Ground and Excited State Electron Transfer Reaction Between a few Anthracene Appended Tertiary Amines and Suitable Electron Acceptors.” 2013. Web. 17 Sep 2019.

Vancouver:

Jomon Jacob P. Ground and Excited State Electron Transfer Reaction Between a few Anthracene Appended Tertiary Amines and Suitable Electron Acceptors. [Internet] [Thesis]. Cochin University of Science and Technology; 2013. [cited 2019 Sep 17]. Available from: http://dyuthi.cusat.ac.in/purl/4625.

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

Council of Science Editors:

Jomon Jacob P. Ground and Excited State Electron Transfer Reaction Between a few Anthracene Appended Tertiary Amines and Suitable Electron Acceptors. [Thesis]. Cochin University of Science and Technology; 2013. Available from: http://dyuthi.cusat.ac.in/purl/4625

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


ETH Zürich

20. Schlicht, Christophe. Model studies toward six-membered ring formation with oxy-ene reactions.

Degree: 2005, ETH Zürich

Subjects/Keywords: ORGANISCH-CHEMISCHE REAKTIONEN + ORGANISCH-CHEMISCHE REAKTIONSMECHANISMEN; DIELS-ALDER-REAKTION + RETRO-DIELS-ALDER-REAKTION (CHEMISCHE REAKTIONEN); ORGANIC REACTIONS + ORGANIC REACTION MECHANISMS; DIELS-ALDER REACTION + RETRO DIELS-ALDER REACTIONS (CHEMICAL REACTIONS); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Schlicht, C. (2005). Model studies toward six-membered ring formation with oxy-ene reactions. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/149090

Chicago Manual of Style (16th Edition):

Schlicht, Christophe. “Model studies toward six-membered ring formation with oxy-ene reactions.” 2005. Doctoral Dissertation, ETH Zürich. Accessed September 17, 2019. http://hdl.handle.net/20.500.11850/149090.

MLA Handbook (7th Edition):

Schlicht, Christophe. “Model studies toward six-membered ring formation with oxy-ene reactions.” 2005. Web. 17 Sep 2019.

Vancouver:

Schlicht C. Model studies toward six-membered ring formation with oxy-ene reactions. [Internet] [Doctoral dissertation]. ETH Zürich; 2005. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/20.500.11850/149090.

Council of Science Editors:

Schlicht C. Model studies toward six-membered ring formation with oxy-ene reactions. [Doctoral Dissertation]. ETH Zürich; 2005. Available from: http://hdl.handle.net/20.500.11850/149090


ETH Zürich

21. Hoffmann, Hermann. Ueber die Oxyde einiger Addukte der Diels-Alderschen Diensynthese.

Degree: 1957, ETH Zürich

Subjects/Keywords: DIELS-ALDER-REAKTION + RETRO-DIELS-ALDER-REAKTION (CHEMISCHE REAKTIONEN); DIENE (ALIPHATISCHE UNGESÄTTIGTE KOHLENWASSERSTOFFE); DIELS-ALDER REACTION + RETRO DIELS-ALDER REACTIONS (CHEMICAL REACTIONS); DIENES (ALIPHATIC UNSATURATED HYDROCARBONS); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Hoffmann, H. (1957). Ueber die Oxyde einiger Addukte der Diels-Alderschen Diensynthese. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/137657

Chicago Manual of Style (16th Edition):

Hoffmann, Hermann. “Ueber die Oxyde einiger Addukte der Diels-Alderschen Diensynthese.” 1957. Doctoral Dissertation, ETH Zürich. Accessed September 17, 2019. http://hdl.handle.net/20.500.11850/137657.

MLA Handbook (7th Edition):

Hoffmann, Hermann. “Ueber die Oxyde einiger Addukte der Diels-Alderschen Diensynthese.” 1957. Web. 17 Sep 2019.

Vancouver:

Hoffmann H. Ueber die Oxyde einiger Addukte der Diels-Alderschen Diensynthese. [Internet] [Doctoral dissertation]. ETH Zürich; 1957. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/20.500.11850/137657.

Council of Science Editors:

Hoffmann H. Ueber die Oxyde einiger Addukte der Diels-Alderschen Diensynthese. [Doctoral Dissertation]. ETH Zürich; 1957. Available from: http://hdl.handle.net/20.500.11850/137657


Indian Institute of Science

22. Ganguly, Bishwajit. Theoretical Studies Of pie-Facial Selectivity In Organic Reactions.

Degree: 1994, Indian Institute of Science

 he thesis entitled "Theoretical Studies of pie-Facial Selectivity in Organic Reactions" involve a computational examination of a suitable reactivity problem in organic chemistry. Systematic and… (more)

Subjects/Keywords: Organic Chemistry; Nucleophilic; Organic Reactions; Electrophilic; Radical and Diels- Alder reactions; Theoretical Studies

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APA (6th Edition):

Ganguly, B. (1994). Theoretical Studies Of pie-Facial Selectivity In Organic Reactions. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/120

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):

Ganguly, Bishwajit. “Theoretical Studies Of pie-Facial Selectivity In Organic Reactions.” 1994. Thesis, Indian Institute of Science. Accessed September 17, 2019. http://hdl.handle.net/2005/120.

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

MLA Handbook (7th Edition):

Ganguly, Bishwajit. “Theoretical Studies Of pie-Facial Selectivity In Organic Reactions.” 1994. Web. 17 Sep 2019.

Vancouver:

Ganguly B. Theoretical Studies Of pie-Facial Selectivity In Organic Reactions. [Internet] [Thesis]. Indian Institute of Science; 1994. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/2005/120.

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

Council of Science Editors:

Ganguly B. Theoretical Studies Of pie-Facial Selectivity In Organic Reactions. [Thesis]. Indian Institute of Science; 1994. Available from: http://hdl.handle.net/2005/120

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

23. Καλόγηρος, Χρήστος. Αντιδράσεις Diels - Alder προστατευμένων ο - βενζοκινονών (MOBs).

Degree: 2007, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

Subjects/Keywords: Αντίδραση Diels-Alder; Προστατευμένη ο - βενζοκινόνη; Οξα - δι - π - μέθανο μετάθεση; Κυκλοιξα - 2.4 - διενόνη; Ρετρο - Diels - Alder αντίδραση; Diels-Alder reactions; Masked o - benzoquinone; Oxa - δι - π - methano rearrengement; Cyclohexa - 2.4 - dienone; Retro - Diels - Alder reaction

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APA (6th Edition):

Καλόγηρος, . . (2007). Αντιδράσεις Diels - Alder προστατευμένων ο - βενζοκινονών (MOBs). (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/21379

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):

Καλόγηρος, Χρήστος. “Αντιδράσεις Diels - Alder προστατευμένων ο - βενζοκινονών (MOBs).” 2007. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed September 17, 2019. http://hdl.handle.net/10442/hedi/21379.

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

MLA Handbook (7th Edition):

Καλόγηρος, Χρήστος. “Αντιδράσεις Diels - Alder προστατευμένων ο - βενζοκινονών (MOBs).” 2007. Web. 17 Sep 2019.

Vancouver:

Καλόγηρος . Αντιδράσεις Diels - Alder προστατευμένων ο - βενζοκινονών (MOBs). [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2007. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10442/hedi/21379.

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

Council of Science Editors:

Καλόγηρος . Αντιδράσεις Diels - Alder προστατευμένων ο - βενζοκινονών (MOBs). [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2007. Available from: http://hdl.handle.net/10442/hedi/21379

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


University of Florida

24. Novak, Bennett H., 1970-. A chemoenzymatic and intramolecular Diels-Alder approach toward the synthesis of morphinan skeletons.

Degree: PhD, Chemistry, 2000, University of Florida

Subjects/Keywords: Acetates; Diels Alder reactions; Dienes; Ethers; Morphine; Room temperature; Silica gel; Skeleton; Stereochemistry; Trienes; Diels-Alder reaction; Morphine; Stereochemistry

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APA (6th Edition):

Novak, Bennett H., 1. (2000). A chemoenzymatic and intramolecular Diels-Alder approach toward the synthesis of morphinan skeletons. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00038447

Chicago Manual of Style (16th Edition):

Novak, Bennett H., 1970-. “A chemoenzymatic and intramolecular Diels-Alder approach toward the synthesis of morphinan skeletons.” 2000. Doctoral Dissertation, University of Florida. Accessed September 17, 2019. http://ufdc.ufl.edu/AA00038447.

MLA Handbook (7th Edition):

Novak, Bennett H., 1970-. “A chemoenzymatic and intramolecular Diels-Alder approach toward the synthesis of morphinan skeletons.” 2000. Web. 17 Sep 2019.

Vancouver:

Novak, Bennett H. 1. A chemoenzymatic and intramolecular Diels-Alder approach toward the synthesis of morphinan skeletons. [Internet] [Doctoral dissertation]. University of Florida; 2000. [cited 2019 Sep 17]. Available from: http://ufdc.ufl.edu/AA00038447.

Council of Science Editors:

Novak, Bennett H. 1. A chemoenzymatic and intramolecular Diels-Alder approach toward the synthesis of morphinan skeletons. [Doctoral Dissertation]. University of Florida; 2000. Available from: http://ufdc.ufl.edu/AA00038447


University of Florida

25. Gum, Andrew G., 1968-. An intramolecular Diels-Alder model study directed toward the synthesis of (-)-morphine.

Degree: 1997, University of Florida

Subjects/Keywords: Acetates; Alcohols; Cycloaddition; Data acquisition; Diels Alder reactions; Dienes; Esters; Ethers; Morphine; Trienes

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APA (6th Edition):

Gum, Andrew G., 1. (1997). An intramolecular Diels-Alder model study directed toward the synthesis of (-)-morphine. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00022848

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):

Gum, Andrew G., 1968-. “An intramolecular Diels-Alder model study directed toward the synthesis of (-)-morphine.” 1997. Thesis, University of Florida. Accessed September 17, 2019. http://ufdc.ufl.edu/AA00022848.

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

MLA Handbook (7th Edition):

Gum, Andrew G., 1968-. “An intramolecular Diels-Alder model study directed toward the synthesis of (-)-morphine.” 1997. Web. 17 Sep 2019.

Vancouver:

Gum, Andrew G. 1. An intramolecular Diels-Alder model study directed toward the synthesis of (-)-morphine. [Internet] [Thesis]. University of Florida; 1997. [cited 2019 Sep 17]. Available from: http://ufdc.ufl.edu/AA00022848.

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

Council of Science Editors:

Gum, Andrew G. 1. An intramolecular Diels-Alder model study directed toward the synthesis of (-)-morphine. [Thesis]. University of Florida; 1997. Available from: http://ufdc.ufl.edu/AA00022848

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

26. PULLARKAT APPUKUTTAN SUMOD. Asymmetric ligand transformation reactions.

Degree: 2005, National University of Singapore

Subjects/Keywords: Chiral auxiliary; Diels-Alder reactions; Asymmetric synthesis; Chiral diphosphines, Terminal alkenols, Hydrophosphination.

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APA (6th Edition):

SUMOD, P. A. (2005). Asymmetric ligand transformation reactions. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/14898

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):

SUMOD, PULLARKAT APPUKUTTAN. “Asymmetric ligand transformation reactions.” 2005. Thesis, National University of Singapore. Accessed September 17, 2019. http://scholarbank.nus.edu.sg/handle/10635/14898.

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

MLA Handbook (7th Edition):

SUMOD, PULLARKAT APPUKUTTAN. “Asymmetric ligand transformation reactions.” 2005. Web. 17 Sep 2019.

Vancouver:

SUMOD PA. Asymmetric ligand transformation reactions. [Internet] [Thesis]. National University of Singapore; 2005. [cited 2019 Sep 17]. Available from: http://scholarbank.nus.edu.sg/handle/10635/14898.

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

Council of Science Editors:

SUMOD PA. Asymmetric ligand transformation reactions. [Thesis]. National University of Singapore; 2005. Available from: http://scholarbank.nus.edu.sg/handle/10635/14898

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


ETH Zürich

27. Piatesi, Andrea. Binding properties and Diels-Alder activity of an efficient antibody catalyst.

Degree: 2003, ETH Zürich

Subjects/Keywords: ANTIKÖRPER + IMMUNOGLOBULINE + GAMMAGLOBULINE (IMMUNOLOGIE); DIELS-ALDER-REAKTION + RETRO-DIELS-ALDER-REAKTION (CHEMISCHE REAKTIONEN); ENZYMREAKTION + ENZYMATISCHER REAKTIONSMECHANISMUS + ENZYMATISCHE KATALYSE (BIOCHEMIE); ANTIBODIES + IMMUNOGLOBULINS + GAMMA GLOBULINS (IMMUNOLOGY); DIELS-ALDER REACTION + RETRO DIELS-ALDER REACTIONS (CHEMICAL REACTIONS); ENZYMATIC REACTIONS + ENZYMATIC REACTION MECHANISM + ENZYMATIC CATALYSIS (BIOCHEMISTRY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Piatesi, A. (2003). Binding properties and Diels-Alder activity of an efficient antibody catalyst. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/147937

Chicago Manual of Style (16th Edition):

Piatesi, Andrea. “Binding properties and Diels-Alder activity of an efficient antibody catalyst.” 2003. Doctoral Dissertation, ETH Zürich. Accessed September 17, 2019. http://hdl.handle.net/20.500.11850/147937.

MLA Handbook (7th Edition):

Piatesi, Andrea. “Binding properties and Diels-Alder activity of an efficient antibody catalyst.” 2003. Web. 17 Sep 2019.

Vancouver:

Piatesi A. Binding properties and Diels-Alder activity of an efficient antibody catalyst. [Internet] [Doctoral dissertation]. ETH Zürich; 2003. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/20.500.11850/147937.

Council of Science Editors:

Piatesi A. Binding properties and Diels-Alder activity of an efficient antibody catalyst. [Doctoral Dissertation]. ETH Zürich; 2003. Available from: http://hdl.handle.net/20.500.11850/147937


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

28. Τερζίδης, Μιχαήλ. Σύνθεση και μελέτη δομής χρωμονικών παραγώγων με πιθανή βιολογική δράση.

Degree: 2010, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

Subjects/Keywords: Χρωμόνες; Αντιδράσεις Diels-Alder; Αντιδράσεις Michael; Αντιδράσεις πολλών συστατικών; Οργανοκατάλυση; Ισοκυανίδια; Ακετυλενοδικαρβοξυλικοί διεστέρες; Τριτοταγείς αρωματικές ετεροκυκλικές αμίνες; Chromones; Diels-Alder reactions; Michael reactions; Multy component reactions; Organocatalysis; Isocyanides; Acetylenediacarboxylates; Tertiary aromatic heterocyclic amines

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APA (6th Edition):

Τερζίδης, . . (2010). Σύνθεση και μελέτη δομής χρωμονικών παραγώγων με πιθανή βιολογική δράση. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/28366

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):

Τερζίδης, Μιχαήλ. “Σύνθεση και μελέτη δομής χρωμονικών παραγώγων με πιθανή βιολογική δράση.” 2010. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed September 17, 2019. http://hdl.handle.net/10442/hedi/28366.

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

MLA Handbook (7th Edition):

Τερζίδης, Μιχαήλ. “Σύνθεση και μελέτη δομής χρωμονικών παραγώγων με πιθανή βιολογική δράση.” 2010. Web. 17 Sep 2019.

Vancouver:

Τερζίδης . Σύνθεση και μελέτη δομής χρωμονικών παραγώγων με πιθανή βιολογική δράση. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2010. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10442/hedi/28366.

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

Council of Science Editors:

Τερζίδης . Σύνθεση και μελέτη δομής χρωμονικών παραγώγων με πιθανή βιολογική δράση. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2010. Available from: http://hdl.handle.net/10442/hedi/28366

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


Johannes Gutenberg Universität Mainz

29. Geisel, Bernhard. Untersuchungen zur stereokontrollierten Synthese von 3-Mercaptolysinderivaten und Untersuchungen zur Synthese von Ansa-Seco-Steroiden.

Degree: 2006, Johannes Gutenberg Universität Mainz

 Untersuchungen zur stereokontrollierten Synthese von 3-Mercaptolysinderivaten: 3-Mercaptolysin und Peptide mit einer 3-Mercaptolysin-Einheit sind als Liganden für Nukleardiagnostika in der Kontrastmittelforschung von großem Interesse. Für das… (more)

Subjects/Keywords: Steroide, Ansa-Steroide, Makrolide, Mitsunobu-Reaktionen, Diels-Alder-Reaktionen, Unnatürliche Aminosäuren, Ozonolysereaktionen, Horner-Reaktionen; Steroids, Ansa-Steroids, Macrolides, Mitsunobu-Reactions, Diels-Alder-Reactions, Unnatural Amino Acids, Ozonolysis, Horner-Reactions; Chemistry and allied sciences

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APA (6th Edition):

Geisel, B. (2006). Untersuchungen zur stereokontrollierten Synthese von 3-Mercaptolysinderivaten und Untersuchungen zur Synthese von Ansa-Seco-Steroiden. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2006/1032/

Chicago Manual of Style (16th Edition):

Geisel, Bernhard. “Untersuchungen zur stereokontrollierten Synthese von 3-Mercaptolysinderivaten und Untersuchungen zur Synthese von Ansa-Seco-Steroiden.” 2006. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 17, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2006/1032/.

MLA Handbook (7th Edition):

Geisel, Bernhard. “Untersuchungen zur stereokontrollierten Synthese von 3-Mercaptolysinderivaten und Untersuchungen zur Synthese von Ansa-Seco-Steroiden.” 2006. Web. 17 Sep 2019.

Vancouver:

Geisel B. Untersuchungen zur stereokontrollierten Synthese von 3-Mercaptolysinderivaten und Untersuchungen zur Synthese von Ansa-Seco-Steroiden. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2006. [cited 2019 Sep 17]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2006/1032/.

Council of Science Editors:

Geisel B. Untersuchungen zur stereokontrollierten Synthese von 3-Mercaptolysinderivaten und Untersuchungen zur Synthese von Ansa-Seco-Steroiden. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2006. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2006/1032/

30. TAN KIEN WEE. Chiral organometallic complexes promoted cycloaddition and insertion reactions.

Degree: 2005, National University of Singapore

Subjects/Keywords: Alkynylphosphines; Arsinophosphines; Asymmetric Diels-Alder reactions; C-H bond activation; C-C bond coupling; Insertion reactions

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APA (6th Edition):

WEE, T. K. (2005). Chiral organometallic complexes promoted cycloaddition and insertion reactions. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/14996

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):

WEE, TAN KIEN. “Chiral organometallic complexes promoted cycloaddition and insertion reactions.” 2005. Thesis, National University of Singapore. Accessed September 17, 2019. http://scholarbank.nus.edu.sg/handle/10635/14996.

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

MLA Handbook (7th Edition):

WEE, TAN KIEN. “Chiral organometallic complexes promoted cycloaddition and insertion reactions.” 2005. Web. 17 Sep 2019.

Vancouver:

WEE TK. Chiral organometallic complexes promoted cycloaddition and insertion reactions. [Internet] [Thesis]. National University of Singapore; 2005. [cited 2019 Sep 17]. Available from: http://scholarbank.nus.edu.sg/handle/10635/14996.

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

Council of Science Editors:

WEE TK. Chiral organometallic complexes promoted cycloaddition and insertion reactions. [Thesis]. National University of Singapore; 2005. Available from: http://scholarbank.nus.edu.sg/handle/10635/14996

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

[1] [2]

.