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

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Oregon State University

1. Schatz, Bruce Stewart. Kinetic studies of some thermal rearrangements.

Degree: PhD, Chemistry, 1966, Oregon State University

Subjects/Keywords: Claisen rearrangement

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APA (6th Edition):

Schatz, B. S. (1966). Kinetic studies of some thermal rearrangements. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/47082

Chicago Manual of Style (16th Edition):

Schatz, Bruce Stewart. “Kinetic studies of some thermal rearrangements.” 1966. Doctoral Dissertation, Oregon State University. Accessed July 13, 2020. http://hdl.handle.net/1957/47082.

MLA Handbook (7th Edition):

Schatz, Bruce Stewart. “Kinetic studies of some thermal rearrangements.” 1966. Web. 13 Jul 2020.

Vancouver:

Schatz BS. Kinetic studies of some thermal rearrangements. [Internet] [Doctoral dissertation]. Oregon State University; 1966. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/1957/47082.

Council of Science Editors:

Schatz BS. Kinetic studies of some thermal rearrangements. [Doctoral Dissertation]. Oregon State University; 1966. Available from: http://hdl.handle.net/1957/47082


Western Washington University

2. Dimmitt, Heidi E. Gold(I)-catalyzed rearrangements of allyl aryl ethers: mechanisitc and synthetic studies.

Degree: MS, Chemistry, 2011, Western Washington University

  Gold catalyzed reactions are an active area of interest for synthetic chemists due to gold's ability to promote formation of carbon-carbon bonds. A mechanistic… (more)

Subjects/Keywords: Chemistry; Catalysts – Synthesis; Claisen rearrangement; masters theses

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APA (6th Edition):

Dimmitt, H. E. (2011). Gold(I)-catalyzed rearrangements of allyl aryl ethers: mechanisitc and synthetic studies. (Masters Thesis). Western Washington University. Retrieved from https://doi.org/10.25710/s2by-y535 ; https://cedar.wwu.edu/wwuet/112

Chicago Manual of Style (16th Edition):

Dimmitt, Heidi E. “Gold(I)-catalyzed rearrangements of allyl aryl ethers: mechanisitc and synthetic studies.” 2011. Masters Thesis, Western Washington University. Accessed July 13, 2020. https://doi.org/10.25710/s2by-y535 ; https://cedar.wwu.edu/wwuet/112.

MLA Handbook (7th Edition):

Dimmitt, Heidi E. “Gold(I)-catalyzed rearrangements of allyl aryl ethers: mechanisitc and synthetic studies.” 2011. Web. 13 Jul 2020.

Vancouver:

Dimmitt HE. Gold(I)-catalyzed rearrangements of allyl aryl ethers: mechanisitc and synthetic studies. [Internet] [Masters thesis]. Western Washington University; 2011. [cited 2020 Jul 13]. Available from: https://doi.org/10.25710/s2by-y535 ; https://cedar.wwu.edu/wwuet/112.

Council of Science Editors:

Dimmitt HE. Gold(I)-catalyzed rearrangements of allyl aryl ethers: mechanisitc and synthetic studies. [Masters Thesis]. Western Washington University; 2011. Available from: https://doi.org/10.25710/s2by-y535 ; https://cedar.wwu.edu/wwuet/112

3. Silva Júnior, Paulo Eliandro da. Estratégias de heterociclização aplicadas a produtos naturais e sintéticos subexplorados pela química medicinal.

Degree: Mestrado, Produtos Naturais e Sintéticos, 2014, University of São Paulo

O presente trabalho divide-se em três capítulos: Capítulo I - Nova síntese de ?-xiloidona: rearranjo de Claisen em hidroxinaftoquinonas; Capítulo II - Síntese e estudo… (more)

Subjects/Keywords: Claisen Rearrangement; Heterociclos; Heterocycles; Naftoquinonas; Naphthoquinones; Rearranjo de Claisen

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APA (6th Edition):

Silva Júnior, P. E. d. (2014). Estratégias de heterociclização aplicadas a produtos naturais e sintéticos subexplorados pela química medicinal. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60138/tde-04062014-112413/ ;

Chicago Manual of Style (16th Edition):

Silva Júnior, Paulo Eliandro da. “Estratégias de heterociclização aplicadas a produtos naturais e sintéticos subexplorados pela química medicinal.” 2014. Masters Thesis, University of São Paulo. Accessed July 13, 2020. http://www.teses.usp.br/teses/disponiveis/60/60138/tde-04062014-112413/ ;.

MLA Handbook (7th Edition):

Silva Júnior, Paulo Eliandro da. “Estratégias de heterociclização aplicadas a produtos naturais e sintéticos subexplorados pela química medicinal.” 2014. Web. 13 Jul 2020.

Vancouver:

Silva Júnior PEd. Estratégias de heterociclização aplicadas a produtos naturais e sintéticos subexplorados pela química medicinal. [Internet] [Masters thesis]. University of São Paulo; 2014. [cited 2020 Jul 13]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60138/tde-04062014-112413/ ;.

Council of Science Editors:

Silva Júnior PEd. Estratégias de heterociclização aplicadas a produtos naturais e sintéticos subexplorados pela química medicinal. [Masters Thesis]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/60/60138/tde-04062014-112413/ ;


Loughborough University

4. Garcia-Torres, Jason. Development of a dual Fries-Claisen rearrangement strategy.

Degree: PhD, 2012, Loughborough University

 Synthetic approaches towards linear fused carbon rings have been developed over the last decades due to their high interest as compounds with potential antibiotic activity… (more)

Subjects/Keywords: 661.8; Fries rearrangement; Claisen rearrangement; Pyranonaphthoquinones; Tetracyclines; Linear fused carbon rings

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APA (6th Edition):

Garcia-Torres, J. (2012). Development of a dual Fries-Claisen rearrangement strategy. (Doctoral Dissertation). Loughborough University. Retrieved from http://hdl.handle.net/2134/11002

Chicago Manual of Style (16th Edition):

Garcia-Torres, Jason. “Development of a dual Fries-Claisen rearrangement strategy.” 2012. Doctoral Dissertation, Loughborough University. Accessed July 13, 2020. http://hdl.handle.net/2134/11002.

MLA Handbook (7th Edition):

Garcia-Torres, Jason. “Development of a dual Fries-Claisen rearrangement strategy.” 2012. Web. 13 Jul 2020.

Vancouver:

Garcia-Torres J. Development of a dual Fries-Claisen rearrangement strategy. [Internet] [Doctoral dissertation]. Loughborough University; 2012. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/2134/11002.

Council of Science Editors:

Garcia-Torres J. Development of a dual Fries-Claisen rearrangement strategy. [Doctoral Dissertation]. Loughborough University; 2012. Available from: http://hdl.handle.net/2134/11002


University of Vermont

5. Yang, Yanbo. Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement.

Degree: PhD, Chemistry, 2014, University of Vermont

  The dissertation describes Pd0-catalyzed formal 1,3-diaza-Claisen rearrangement and the design and development of cationic 1,3-diaza-Claisen rearrangement. Our previous work has shown that isocyanates react… (more)

Subjects/Keywords: 1; 3-diaza-Claisen rearrangement; Cationic [3; 3] rearrangement; Pd(0) [3; 3] rearrangement; Chemistry

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APA (6th Edition):

Yang, Y. (2014). Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/261

Chicago Manual of Style (16th Edition):

Yang, Yanbo. “Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement.” 2014. Doctoral Dissertation, University of Vermont. Accessed July 13, 2020. https://scholarworks.uvm.edu/graddis/261.

MLA Handbook (7th Edition):

Yang, Yanbo. “Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement.” 2014. Web. 13 Jul 2020.

Vancouver:

Yang Y. Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement. [Internet] [Doctoral dissertation]. University of Vermont; 2014. [cited 2020 Jul 13]. Available from: https://scholarworks.uvm.edu/graddis/261.

Council of Science Editors:

Yang Y. Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement. [Doctoral Dissertation]. University of Vermont; 2014. Available from: https://scholarworks.uvm.edu/graddis/261


University of Arkansas

6. Rivero-Castro, Juliette. Towards the Total Synthesis of Antascomicin B. Efforts to Construct the C1-C21 Fragment.

Degree: PhD, 2013, University of Arkansas

  Antascomicin B is a macrolide isolated from a strain of Micromonospora. It possesses structural similarities to FK506 and rapamycin and exhibits potent binding ability… (more)

Subjects/Keywords: Pure sciences; Amide bond formation; Amino-claisen rearrangement; Antascomicin B; FKBP12; Ireland-Claisen rearrangement; Ring-closing olefin metathesis; Organic Chemistry

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APA (6th Edition):

Rivero-Castro, J. (2013). Towards the Total Synthesis of Antascomicin B. Efforts to Construct the C1-C21 Fragment. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/973

Chicago Manual of Style (16th Edition):

Rivero-Castro, Juliette. “Towards the Total Synthesis of Antascomicin B. Efforts to Construct the C1-C21 Fragment.” 2013. Doctoral Dissertation, University of Arkansas. Accessed July 13, 2020. https://scholarworks.uark.edu/etd/973.

MLA Handbook (7th Edition):

Rivero-Castro, Juliette. “Towards the Total Synthesis of Antascomicin B. Efforts to Construct the C1-C21 Fragment.” 2013. Web. 13 Jul 2020.

Vancouver:

Rivero-Castro J. Towards the Total Synthesis of Antascomicin B. Efforts to Construct the C1-C21 Fragment. [Internet] [Doctoral dissertation]. University of Arkansas; 2013. [cited 2020 Jul 13]. Available from: https://scholarworks.uark.edu/etd/973.

Council of Science Editors:

Rivero-Castro J. Towards the Total Synthesis of Antascomicin B. Efforts to Construct the C1-C21 Fragment. [Doctoral Dissertation]. University of Arkansas; 2013. Available from: https://scholarworks.uark.edu/etd/973


NSYSU

7. Jhang, You-min. Synthesis of Bicyclic Tetrahydrothiophene Derivatives.

Degree: Master, Chemistry, 2017, NSYSU

 Tetrahydrothiophene derivatives are commonly found in the structures of natural products, these biologically active tetrahydrothiophene derivatives can be used as medicinal drugs. Tetrahydrothiophene derivatives also… (more)

Subjects/Keywords: cyclopenta[c]thiophene; Ruthenium catalyzed ring-closing metathesis; Claisen / Overman rearrangement

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APA (6th Edition):

Jhang, Y. (2017). Synthesis of Bicyclic Tetrahydrothiophene Derivatives. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-174815

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):

Jhang, You-min. “Synthesis of Bicyclic Tetrahydrothiophene Derivatives.” 2017. Thesis, NSYSU. Accessed July 13, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-174815.

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

MLA Handbook (7th Edition):

Jhang, You-min. “Synthesis of Bicyclic Tetrahydrothiophene Derivatives.” 2017. Web. 13 Jul 2020.

Vancouver:

Jhang Y. Synthesis of Bicyclic Tetrahydrothiophene Derivatives. [Internet] [Thesis]. NSYSU; 2017. [cited 2020 Jul 13]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-174815.

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

Council of Science Editors:

Jhang Y. Synthesis of Bicyclic Tetrahydrothiophene Derivatives. [Thesis]. NSYSU; 2017. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708117-174815

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


Boston College

8. Ishibashi, Jacob Shotaro Afaga. BN Isosteres of Acenes for Potential Applications in Optoelectronic Devices.

Degree: PhD, Chemistry, 2017, Boston College

 This dissertation describes progress in the field of polycyclic boron- nitrogen-containing systems, especially for potential application in organic-based optoelectronic devices and hydrogen storage materials. The… (more)

Subjects/Keywords: Acenes; Azaborines; Claisen Rearrangement; Hydrogen Storage; Optoelectronic Properties; Organic Synthesis

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APA (6th Edition):

Ishibashi, J. S. A. (2017). BN Isosteres of Acenes for Potential Applications in Optoelectronic Devices. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107613

Chicago Manual of Style (16th Edition):

Ishibashi, Jacob Shotaro Afaga. “BN Isosteres of Acenes for Potential Applications in Optoelectronic Devices.” 2017. Doctoral Dissertation, Boston College. Accessed July 13, 2020. http://dlib.bc.edu/islandora/object/bc-ir:107613.

MLA Handbook (7th Edition):

Ishibashi, Jacob Shotaro Afaga. “BN Isosteres of Acenes for Potential Applications in Optoelectronic Devices.” 2017. Web. 13 Jul 2020.

Vancouver:

Ishibashi JSA. BN Isosteres of Acenes for Potential Applications in Optoelectronic Devices. [Internet] [Doctoral dissertation]. Boston College; 2017. [cited 2020 Jul 13]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107613.

Council of Science Editors:

Ishibashi JSA. BN Isosteres of Acenes for Potential Applications in Optoelectronic Devices. [Doctoral Dissertation]. Boston College; 2017. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107613


Michigan State University

9. Cook, Gregory Richard. The preparation and charge promoted aza-Claisen rearrangement of N-allylenamines.

Degree: MS, Department of Chemistry, 1990, Michigan State University

Subjects/Keywords: Claisen rearrangement; Amines; Nitrogen

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APA (6th Edition):

Cook, G. R. (1990). The preparation and charge promoted aza-Claisen rearrangement of N-allylenamines. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:21723

Chicago Manual of Style (16th Edition):

Cook, Gregory Richard. “The preparation and charge promoted aza-Claisen rearrangement of N-allylenamines.” 1990. Masters Thesis, Michigan State University. Accessed July 13, 2020. http://etd.lib.msu.edu/islandora/object/etd:21723.

MLA Handbook (7th Edition):

Cook, Gregory Richard. “The preparation and charge promoted aza-Claisen rearrangement of N-allylenamines.” 1990. Web. 13 Jul 2020.

Vancouver:

Cook GR. The preparation and charge promoted aza-Claisen rearrangement of N-allylenamines. [Internet] [Masters thesis]. Michigan State University; 1990. [cited 2020 Jul 13]. Available from: http://etd.lib.msu.edu/islandora/object/etd:21723.

Council of Science Editors:

Cook GR. The preparation and charge promoted aza-Claisen rearrangement of N-allylenamines. [Masters Thesis]. Michigan State University; 1990. Available from: http://etd.lib.msu.edu/islandora/object/etd:21723


University of New Mexico

10. Chen, Xiaobei. STUDY OF NOVEL SYNTHETIC METHODOLOGIES FOR INDOLYL DERIVATIVES AND BETA-FLUOROENALS.

Degree: Department of Chemistry and Chemical Biology, 2015, University of New Mexico

  One of the central goals in modern organic synthesis is to develop efficient synthetic strategies for the preparation and study of complex molecules possessing… (more)

Subjects/Keywords: aza-Claisen rearrangement; Prins cyclization; conjugate addition; Chemistry; Physical Chemistry

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APA (6th Edition):

Chen, X. (2015). STUDY OF NOVEL SYNTHETIC METHODOLOGIES FOR INDOLYL DERIVATIVES AND BETA-FLUOROENALS. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/chem_etds/44

Chicago Manual of Style (16th Edition):

Chen, Xiaobei. “STUDY OF NOVEL SYNTHETIC METHODOLOGIES FOR INDOLYL DERIVATIVES AND BETA-FLUOROENALS.” 2015. Doctoral Dissertation, University of New Mexico. Accessed July 13, 2020. https://digitalrepository.unm.edu/chem_etds/44.

MLA Handbook (7th Edition):

Chen, Xiaobei. “STUDY OF NOVEL SYNTHETIC METHODOLOGIES FOR INDOLYL DERIVATIVES AND BETA-FLUOROENALS.” 2015. Web. 13 Jul 2020.

Vancouver:

Chen X. STUDY OF NOVEL SYNTHETIC METHODOLOGIES FOR INDOLYL DERIVATIVES AND BETA-FLUOROENALS. [Internet] [Doctoral dissertation]. University of New Mexico; 2015. [cited 2020 Jul 13]. Available from: https://digitalrepository.unm.edu/chem_etds/44.

Council of Science Editors:

Chen X. STUDY OF NOVEL SYNTHETIC METHODOLOGIES FOR INDOLYL DERIVATIVES AND BETA-FLUOROENALS. [Doctoral Dissertation]. University of New Mexico; 2015. Available from: https://digitalrepository.unm.edu/chem_etds/44


University of St. Andrews

11. Voûte, Nicholas. Rearrangements in the indolo[2,3-b]quinoline system : a novel approach to the synthesis of perophoramidine and the the communesins .

Degree: 2008, University of St. Andrews

 This thesis describes investigations directed towards developing a novel synthetic route to the natural products perophoramidine and the communesins, with particular emphasis placed on the… (more)

Subjects/Keywords: Communesin; Perophoramidine; Claisen rearrangement

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APA (6th Edition):

Voûte, N. (2008). Rearrangements in the indolo[2,3-b]quinoline system : a novel approach to the synthesis of perophoramidine and the the communesins . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/486

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):

Voûte, Nicholas. “Rearrangements in the indolo[2,3-b]quinoline system : a novel approach to the synthesis of perophoramidine and the the communesins .” 2008. Thesis, University of St. Andrews. Accessed July 13, 2020. http://hdl.handle.net/10023/486.

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

MLA Handbook (7th Edition):

Voûte, Nicholas. “Rearrangements in the indolo[2,3-b]quinoline system : a novel approach to the synthesis of perophoramidine and the the communesins .” 2008. Web. 13 Jul 2020.

Vancouver:

Voûte N. Rearrangements in the indolo[2,3-b]quinoline system : a novel approach to the synthesis of perophoramidine and the the communesins . [Internet] [Thesis]. University of St. Andrews; 2008. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/10023/486.

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

Council of Science Editors:

Voûte N. Rearrangements in the indolo[2,3-b]quinoline system : a novel approach to the synthesis of perophoramidine and the the communesins . [Thesis]. University of St. Andrews; 2008. Available from: http://hdl.handle.net/10023/486

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

12. Ernouf, Guillaume. Réarrangements sigmatropiques - Synthèse de cyclopropanes fonctionnalisés : Sigmatropic rearrangements - Synthesis of functionalized cyclopropanes.

Degree: Docteur es, Chimie Organique, 2016, Université Pierre et Marie Curie – Paris VI

Les cyclopropanes sont rencontrés dans de nombreux produits naturels ou synthétiques bioactifs. Les travaux exposés dans ce manuscrit portent sur le développement de réarrangements sigmatropiques… (more)

Subjects/Keywords: Cyclopropènes; Alkylidènecyclopropanes; Cyclopropanes; Réarrangements sigmatropiques; Réarrangement d'Ireland-Claisen; Diastéréosélectivité; Sigmatropic rearrangement; Alkylidenecyclopropanes; Diastereoselectivity; 547

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APA (6th Edition):

Ernouf, G. (2016). Réarrangements sigmatropiques - Synthèse de cyclopropanes fonctionnalisés : Sigmatropic rearrangements - Synthesis of functionalized cyclopropanes. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066719

Chicago Manual of Style (16th Edition):

Ernouf, Guillaume. “Réarrangements sigmatropiques - Synthèse de cyclopropanes fonctionnalisés : Sigmatropic rearrangements - Synthesis of functionalized cyclopropanes.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed July 13, 2020. http://www.theses.fr/2016PA066719.

MLA Handbook (7th Edition):

Ernouf, Guillaume. “Réarrangements sigmatropiques - Synthèse de cyclopropanes fonctionnalisés : Sigmatropic rearrangements - Synthesis of functionalized cyclopropanes.” 2016. Web. 13 Jul 2020.

Vancouver:

Ernouf G. Réarrangements sigmatropiques - Synthèse de cyclopropanes fonctionnalisés : Sigmatropic rearrangements - Synthesis of functionalized cyclopropanes. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2016PA066719.

Council of Science Editors:

Ernouf G. Réarrangements sigmatropiques - Synthèse de cyclopropanes fonctionnalisés : Sigmatropic rearrangements - Synthesis of functionalized cyclopropanes. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066719


University of Pennsylvania

13. Cao, Trung Duy Chi. Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols .

Degree: 2013, University of Pennsylvania

 Part A. The first catalytic, enantioselective Saucy-Marbet Claisen rearrangement has been developed. Palladium(II) catalysts with BINAP or t-BuPHOX ligands were discovered as superior in catalyzing… (more)

Subjects/Keywords: Claisen rerrangement; High-troughput experimentation; Phenol oxidative coupling; sigmatropic rearrangement; Chemistry; Organic Chemistry

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APA (6th Edition):

Cao, T. D. C. (2013). Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/619

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):

Cao, Trung Duy Chi. “Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols .” 2013. Thesis, University of Pennsylvania. Accessed July 13, 2020. https://repository.upenn.edu/edissertations/619.

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

MLA Handbook (7th Edition):

Cao, Trung Duy Chi. “Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols .” 2013. Web. 13 Jul 2020.

Vancouver:

Cao TDC. Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2020 Jul 13]. Available from: https://repository.upenn.edu/edissertations/619.

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

Council of Science Editors:

Cao TDC. Part A: Palladium(II)-Catalyzed Enantioselective Saucy-Marbet Claisen Rearrangement of Propargyloxy indoles to Quaternary Oxindoles and Spirocyclic Lactones. Part B: The Regioselective Oxidative Coupling of Phenols . [Thesis]. University of Pennsylvania; 2013. Available from: https://repository.upenn.edu/edissertations/619

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


Boston University

14. Xiong, Yuan. Total syntheses of sanggenon-type natural products and rearrangements of 3-substituted flavone ethers.

Degree: PhD, Chemistry, 2014, Boston University

 An efficient approach to the hydrobenzofuro[3,2-b]chromenone core of sanggenon-type natural products has been developed. The key transformation involves a protecting group-free double rearrangement of a… (more)

Subjects/Keywords: Organic chemistry; Diels-Alder cycloaddition; Asymmetric Claisen rearrangement; Cycloisomerization; Furanyl benzofuranone; Natural product synthesis; Sanggenons

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APA (6th Edition):

Xiong, Y. (2014). Total syntheses of sanggenon-type natural products and rearrangements of 3-substituted flavone ethers. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/14142

Chicago Manual of Style (16th Edition):

Xiong, Yuan. “Total syntheses of sanggenon-type natural products and rearrangements of 3-substituted flavone ethers.” 2014. Doctoral Dissertation, Boston University. Accessed July 13, 2020. http://hdl.handle.net/2144/14142.

MLA Handbook (7th Edition):

Xiong, Yuan. “Total syntheses of sanggenon-type natural products and rearrangements of 3-substituted flavone ethers.” 2014. Web. 13 Jul 2020.

Vancouver:

Xiong Y. Total syntheses of sanggenon-type natural products and rearrangements of 3-substituted flavone ethers. [Internet] [Doctoral dissertation]. Boston University; 2014. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/2144/14142.

Council of Science Editors:

Xiong Y. Total syntheses of sanggenon-type natural products and rearrangements of 3-substituted flavone ethers. [Doctoral Dissertation]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14142

15. O'Rourke, Natasha Felicia. Mechanistic Studies of Orthogonal Transformations of Bis-Vinyl Ethers: Modular Access to Complex Small Molecules.

Degree: Department of Chemistry, 2014, University of Victoria

 Efficient access to molecular complexity and diversity is important for the development of small-molecule screening libraries designed to identify highly specific modulators of disease relevant… (more)

Subjects/Keywords: organic chemistry; Claisen rearrangement; radical cyclization; cascade; iterative synthesis; complex small molecules

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APA (6th Edition):

O'Rourke, N. F. (2014). Mechanistic Studies of Orthogonal Transformations of Bis-Vinyl Ethers: Modular Access to Complex Small Molecules. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/5730

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):

O'Rourke, Natasha Felicia. “Mechanistic Studies of Orthogonal Transformations of Bis-Vinyl Ethers: Modular Access to Complex Small Molecules.” 2014. Thesis, University of Victoria. Accessed July 13, 2020. http://hdl.handle.net/1828/5730.

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

MLA Handbook (7th Edition):

O'Rourke, Natasha Felicia. “Mechanistic Studies of Orthogonal Transformations of Bis-Vinyl Ethers: Modular Access to Complex Small Molecules.” 2014. Web. 13 Jul 2020.

Vancouver:

O'Rourke NF. Mechanistic Studies of Orthogonal Transformations of Bis-Vinyl Ethers: Modular Access to Complex Small Molecules. [Internet] [Thesis]. University of Victoria; 2014. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/1828/5730.

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

Council of Science Editors:

O'Rourke NF. Mechanistic Studies of Orthogonal Transformations of Bis-Vinyl Ethers: Modular Access to Complex Small Molecules. [Thesis]. University of Victoria; 2014. Available from: http://hdl.handle.net/1828/5730

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


Uniwersytet im. Adama Mickiewicza w Poznaniu

16. Marciniak, Bartosz. Przegrupowanie Claisena fluorowanych eterów allilowo-winylowych i jego zastosowanie w syntezie organicznej .

Degree: 2014, Uniwersytet im. Adama Mickiewicza w Poznaniu

 Rozprawa dotyczy wyników badań prowadzonych nad przegrupowaniem Claisena fluorowanych eterów allilowo-winylowych, które pozwala otrzymać α-trifluorometylo-γ,δ-nienasycone związki karbonylowe. Produkty przegrupowania zostały następnie zastosowane w syntezie organicznej.… (more)

Subjects/Keywords: fluor; fluorine; przegrupowanie Claisena; claisen rearrangement; etery allilowo-winylowe; allyl-vinyl ethers; halofluorowanie; halofluorination

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APA (6th Edition):

Marciniak, B. (2014). Przegrupowanie Claisena fluorowanych eterów allilowo-winylowych i jego zastosowanie w syntezie organicznej . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/10983

Chicago Manual of Style (16th Edition):

Marciniak, Bartosz. “Przegrupowanie Claisena fluorowanych eterów allilowo-winylowych i jego zastosowanie w syntezie organicznej .” 2014. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed July 13, 2020. http://hdl.handle.net/10593/10983.

MLA Handbook (7th Edition):

Marciniak, Bartosz. “Przegrupowanie Claisena fluorowanych eterów allilowo-winylowych i jego zastosowanie w syntezie organicznej .” 2014. Web. 13 Jul 2020.

Vancouver:

Marciniak B. Przegrupowanie Claisena fluorowanych eterów allilowo-winylowych i jego zastosowanie w syntezie organicznej . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2014. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/10593/10983.

Council of Science Editors:

Marciniak B. Przegrupowanie Claisena fluorowanych eterów allilowo-winylowych i jego zastosowanie w syntezie organicznej . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2014. Available from: http://hdl.handle.net/10593/10983


University of Hong Kong

17. 王港政. Studies on the copper hydride mediated reductive Claisenrearrangement.

Degree: 2013, University of Hong Kong

Subjects/Keywords: Claisen rearrangement.; Reduction (Chemistry); Copper compounds.

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APA (6th Edition):

王港政.. (2013). Studies on the copper hydride mediated reductive Claisenrearrangement. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/192821

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

Chicago Manual of Style (16th Edition):

王港政.. “Studies on the copper hydride mediated reductive Claisenrearrangement.” 2013. Thesis, University of Hong Kong. Accessed July 13, 2020. http://hdl.handle.net/10722/192821.

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

MLA Handbook (7th Edition):

王港政.. “Studies on the copper hydride mediated reductive Claisenrearrangement.” 2013. Web. 13 Jul 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

王港政.. Studies on the copper hydride mediated reductive Claisenrearrangement. [Internet] [Thesis]. University of Hong Kong; 2013. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/10722/192821.

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

Council of Science Editors:

王港政.. Studies on the copper hydride mediated reductive Claisenrearrangement. [Thesis]. University of Hong Kong; 2013. Available from: http://hdl.handle.net/10722/192821

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


Indian Institute of Science

18. Vasanthalakshmi, B. Ireland-Claisen Rearrangement Based Strategy To Sesquiterpenes Containing Vicinal Quaternary Carbon Atoms.

Degree: 2006, Indian Institute of Science

 Among Nature's creation, terpenoids are more versatile and exciting natural products. In a remarkable display of synthetic ingenuity and creativity, nature has endowed terpenes with… (more)

Subjects/Keywords: Molecular Structure; Sesquiterpenes; Carbon Atoms; Sesquiterpenes - Synthesis; Olefin Metathesis; Claisen Rearrangement; Herbertenes - Synthesis; Spirobenzofuran - Synthesis; Lagopodin - Synthesis; Laurencenone - Synthesis; Ireland-Claisen; Organic Chemistry

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APA (6th Edition):

Vasanthalakshmi, B. (2006). Ireland-Claisen Rearrangement Based Strategy To Sesquiterpenes Containing Vicinal Quaternary Carbon Atoms. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/390

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):

Vasanthalakshmi, B. “Ireland-Claisen Rearrangement Based Strategy To Sesquiterpenes Containing Vicinal Quaternary Carbon Atoms.” 2006. Thesis, Indian Institute of Science. Accessed July 13, 2020. http://hdl.handle.net/2005/390.

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

MLA Handbook (7th Edition):

Vasanthalakshmi, B. “Ireland-Claisen Rearrangement Based Strategy To Sesquiterpenes Containing Vicinal Quaternary Carbon Atoms.” 2006. Web. 13 Jul 2020.

Vancouver:

Vasanthalakshmi B. Ireland-Claisen Rearrangement Based Strategy To Sesquiterpenes Containing Vicinal Quaternary Carbon Atoms. [Internet] [Thesis]. Indian Institute of Science; 2006. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/2005/390.

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

Council of Science Editors:

Vasanthalakshmi B. Ireland-Claisen Rearrangement Based Strategy To Sesquiterpenes Containing Vicinal Quaternary Carbon Atoms. [Thesis]. Indian Institute of Science; 2006. Available from: http://hdl.handle.net/2005/390

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


Johannes Gutenberg Universität Mainz

19. 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 July 13, 2020. 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. 13 Jul 2020.

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 2020 Jul 13]. 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

20. Kinney, Wiliam Alvin. Part I: A vinyl sulfone-mediated Diels-Alder approach to the regiocontrolled elaboration of 2-cyclohexenones ; Part II: Construction of fused 4-cyclooctenones by Claisen rearrangement and approaches to the synthesis of precapnelladiene.

Degree: PhD, Graduate School, 1984, The Ohio State University

Subjects/Keywords: Chemistry; Sulfones; Diels-Alder reaction; Claisen rearrangement

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APA (6th Edition):

Kinney, W. A. (1984). Part I: A vinyl sulfone-mediated Diels-Alder approach to the regiocontrolled elaboration of 2-cyclohexenones ; Part II: Construction of fused 4-cyclooctenones by Claisen rearrangement and approaches to the synthesis of precapnelladiene. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487253838525243

Chicago Manual of Style (16th Edition):

Kinney, Wiliam Alvin. “Part I: A vinyl sulfone-mediated Diels-Alder approach to the regiocontrolled elaboration of 2-cyclohexenones ; Part II: Construction of fused 4-cyclooctenones by Claisen rearrangement and approaches to the synthesis of precapnelladiene.” 1984. Doctoral Dissertation, The Ohio State University. Accessed July 13, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487253838525243.

MLA Handbook (7th Edition):

Kinney, Wiliam Alvin. “Part I: A vinyl sulfone-mediated Diels-Alder approach to the regiocontrolled elaboration of 2-cyclohexenones ; Part II: Construction of fused 4-cyclooctenones by Claisen rearrangement and approaches to the synthesis of precapnelladiene.” 1984. Web. 13 Jul 2020.

Vancouver:

Kinney WA. Part I: A vinyl sulfone-mediated Diels-Alder approach to the regiocontrolled elaboration of 2-cyclohexenones ; Part II: Construction of fused 4-cyclooctenones by Claisen rearrangement and approaches to the synthesis of precapnelladiene. [Internet] [Doctoral dissertation]. The Ohio State University; 1984. [cited 2020 Jul 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487253838525243.

Council of Science Editors:

Kinney WA. Part I: A vinyl sulfone-mediated Diels-Alder approach to the regiocontrolled elaboration of 2-cyclohexenones ; Part II: Construction of fused 4-cyclooctenones by Claisen rearrangement and approaches to the synthesis of precapnelladiene. [Doctoral Dissertation]. The Ohio State University; 1984. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487253838525243


Indian Institute of Science

21. Babu, R Ramesh. Total Synthesis Of Sesquiterpenes Acorenols, Chamigrenes And Laurokamurene B; And Enantiospecific Synthesis Of ABC-Ring System Of A-Nor And Abeo Pentacyclic Triterpenes.

Degree: 2009, Indian Institute of Science

 Among Nature’s creation, terpenoids are more versatile and exciting natural products. In a remarkable display of synthetic ingenuity and creativity, nature has endowed terpenes with… (more)

Subjects/Keywords: Sesquiterpenes Synthesis; Triterpenes - Synthesis; Acorenols; Chamigrene; Laurencenone; Laurokamurene; Olefin Metathesis; Claisen Rearrangement; Pentacyclic Triterpenes; Organic Chemistry

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APA (6th Edition):

Babu, R. R. (2009). Total Synthesis Of Sesquiterpenes Acorenols, Chamigrenes And Laurokamurene B; And Enantiospecific Synthesis Of ABC-Ring System Of A-Nor And Abeo Pentacyclic Triterpenes. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/1022

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):

Babu, R Ramesh. “Total Synthesis Of Sesquiterpenes Acorenols, Chamigrenes And Laurokamurene B; And Enantiospecific Synthesis Of ABC-Ring System Of A-Nor And Abeo Pentacyclic Triterpenes.” 2009. Thesis, Indian Institute of Science. Accessed July 13, 2020. http://hdl.handle.net/2005/1022.

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

MLA Handbook (7th Edition):

Babu, R Ramesh. “Total Synthesis Of Sesquiterpenes Acorenols, Chamigrenes And Laurokamurene B; And Enantiospecific Synthesis Of ABC-Ring System Of A-Nor And Abeo Pentacyclic Triterpenes.” 2009. Web. 13 Jul 2020.

Vancouver:

Babu RR. Total Synthesis Of Sesquiterpenes Acorenols, Chamigrenes And Laurokamurene B; And Enantiospecific Synthesis Of ABC-Ring System Of A-Nor And Abeo Pentacyclic Triterpenes. [Internet] [Thesis]. Indian Institute of Science; 2009. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/2005/1022.

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

Council of Science Editors:

Babu RR. Total Synthesis Of Sesquiterpenes Acorenols, Chamigrenes And Laurokamurene B; And Enantiospecific Synthesis Of ABC-Ring System Of A-Nor And Abeo Pentacyclic Triterpenes. [Thesis]. Indian Institute of Science; 2009. Available from: http://hdl.handle.net/2005/1022

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

22. Walker, Joel. Generation Of Electron Deficient Carbodiimides And Their Application In The Guanidine Forming, Zwitterionic 1,3-Diaza-Claisen Rearrangement.

Degree: PhD, Chemistry, 2017, University of Vermont

  The 1,3-diaza Claisen rearrangement was initially discovered by the Madalengoitia group in the early 2000s. Tertiary, allylic, amines nucleophilically add to the carbon of… (more)

Subjects/Keywords: 1,3-diaza Claisen rearrangement; Carbodiimides; Organic Chemistry

…1,3diaza Claisen rearrangement… …89 vi LIST OF FIGURES AND SCHEMES Figure 1.1. The generic Claisen rearrangement… …1 Figure 1.2. Acyclic Claisen rearrangement: chair-like transition states… …4 Scheme 1.1. Mariano’s zwitterionic 3-aza Claisen rearrangement… …4 Figure 1.5. The general zwitterionic 1,3-diaza Claisen rearrangement… 

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APA (6th Edition):

Walker, J. (2017). Generation Of Electron Deficient Carbodiimides And Their Application In The Guanidine Forming, Zwitterionic 1,3-Diaza-Claisen Rearrangement. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/674

Chicago Manual of Style (16th Edition):

Walker, Joel. “Generation Of Electron Deficient Carbodiimides And Their Application In The Guanidine Forming, Zwitterionic 1,3-Diaza-Claisen Rearrangement.” 2017. Doctoral Dissertation, University of Vermont. Accessed July 13, 2020. https://scholarworks.uvm.edu/graddis/674.

MLA Handbook (7th Edition):

Walker, Joel. “Generation Of Electron Deficient Carbodiimides And Their Application In The Guanidine Forming, Zwitterionic 1,3-Diaza-Claisen Rearrangement.” 2017. Web. 13 Jul 2020.

Vancouver:

Walker J. Generation Of Electron Deficient Carbodiimides And Their Application In The Guanidine Forming, Zwitterionic 1,3-Diaza-Claisen Rearrangement. [Internet] [Doctoral dissertation]. University of Vermont; 2017. [cited 2020 Jul 13]. Available from: https://scholarworks.uvm.edu/graddis/674.

Council of Science Editors:

Walker J. Generation Of Electron Deficient Carbodiimides And Their Application In The Guanidine Forming, Zwitterionic 1,3-Diaza-Claisen Rearrangement. [Doctoral Dissertation]. University of Vermont; 2017. Available from: https://scholarworks.uvm.edu/graddis/674


University of Oxford

23. Knott, Jane Marie. Studies on Pyridine n-oxides.

Degree: PhD, 1995, University of Oxford

 The work described herein is directed towards the Claisen rearrangements and [3+2] cycloaddition reaction of pyridine N-oxide systems. The pyridine N-oxide molecule is a very… (more)

Subjects/Keywords: 547; Pyridine : Derivatives : Synthesis : Claisen rearrangement : Ring formation (Chemistry)

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APA (6th Edition):

Knott, J. M. (1995). Studies on Pyridine n-oxides. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:cc74d06b-9840-4695-9f47-961583da147c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308591

Chicago Manual of Style (16th Edition):

Knott, Jane Marie. “Studies on Pyridine n-oxides.” 1995. Doctoral Dissertation, University of Oxford. Accessed July 13, 2020. http://ora.ox.ac.uk/objects/uuid:cc74d06b-9840-4695-9f47-961583da147c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308591.

MLA Handbook (7th Edition):

Knott, Jane Marie. “Studies on Pyridine n-oxides.” 1995. Web. 13 Jul 2020.

Vancouver:

Knott JM. Studies on Pyridine n-oxides. [Internet] [Doctoral dissertation]. University of Oxford; 1995. [cited 2020 Jul 13]. Available from: http://ora.ox.ac.uk/objects/uuid:cc74d06b-9840-4695-9f47-961583da147c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308591.

Council of Science Editors:

Knott JM. Studies on Pyridine n-oxides. [Doctoral Dissertation]. University of Oxford; 1995. Available from: http://ora.ox.ac.uk/objects/uuid:cc74d06b-9840-4695-9f47-961583da147c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.308591


University of Bath

24. Tellam, James Peter. An Ireland-Claisen approach to beta-hydroxy alpha-amino acids.

Degree: PhD, 2010, University of Bath

Subjects/Keywords: 547.7; beta-hydroxy alpha-amino acids; rearrangement; Ireland-Claisen

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APA (6th Edition):

Tellam, J. P. (2010). An Ireland-Claisen approach to beta-hydroxy alpha-amino acids. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/an-irelandclaisen-approach-to-betahydroxy-alphaamino-acids(7aaf4168-2dbd-478b-902b-0fd956c1eda9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541238

Chicago Manual of Style (16th Edition):

Tellam, James Peter. “An Ireland-Claisen approach to beta-hydroxy alpha-amino acids.” 2010. Doctoral Dissertation, University of Bath. Accessed July 13, 2020. https://researchportal.bath.ac.uk/en/studentthesis/an-irelandclaisen-approach-to-betahydroxy-alphaamino-acids(7aaf4168-2dbd-478b-902b-0fd956c1eda9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541238.

MLA Handbook (7th Edition):

Tellam, James Peter. “An Ireland-Claisen approach to beta-hydroxy alpha-amino acids.” 2010. Web. 13 Jul 2020.

Vancouver:

Tellam JP. An Ireland-Claisen approach to beta-hydroxy alpha-amino acids. [Internet] [Doctoral dissertation]. University of Bath; 2010. [cited 2020 Jul 13]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/an-irelandclaisen-approach-to-betahydroxy-alphaamino-acids(7aaf4168-2dbd-478b-902b-0fd956c1eda9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541238.

Council of Science Editors:

Tellam JP. An Ireland-Claisen approach to beta-hydroxy alpha-amino acids. [Doctoral Dissertation]. University of Bath; 2010. Available from: https://researchportal.bath.ac.uk/en/studentthesis/an-irelandclaisen-approach-to-betahydroxy-alphaamino-acids(7aaf4168-2dbd-478b-902b-0fd956c1eda9).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.541238


Michigan State University

25. Voss, David Phillip. The Lewis acid catalyzed aza-Claisen rearrangement of allylenamines.

Degree: MS, Department of Chemistry, 1990, Michigan State University

Subjects/Keywords: Lewis acids; Claisen rearrangement; Acid-base chemistry

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APA (6th Edition):

Voss, D. P. (1990). The Lewis acid catalyzed aza-Claisen rearrangement of allylenamines. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:22711

Chicago Manual of Style (16th Edition):

Voss, David Phillip. “The Lewis acid catalyzed aza-Claisen rearrangement of allylenamines.” 1990. Masters Thesis, Michigan State University. Accessed July 13, 2020. http://etd.lib.msu.edu/islandora/object/etd:22711.

MLA Handbook (7th Edition):

Voss, David Phillip. “The Lewis acid catalyzed aza-Claisen rearrangement of allylenamines.” 1990. Web. 13 Jul 2020.

Vancouver:

Voss DP. The Lewis acid catalyzed aza-Claisen rearrangement of allylenamines. [Internet] [Masters thesis]. Michigan State University; 1990. [cited 2020 Jul 13]. Available from: http://etd.lib.msu.edu/islandora/object/etd:22711.

Council of Science Editors:

Voss DP. The Lewis acid catalyzed aza-Claisen rearrangement of allylenamines. [Masters Thesis]. Michigan State University; 1990. Available from: http://etd.lib.msu.edu/islandora/object/etd:22711


University of Hong Kong

26. Ng, Wang-hei. Studies on the copper hydride mediated reductive Claisen rearrangement & synthesis and synthetic applications of C- boron enolates.

Degree: 2016, University of Hong Kong

 The copper hydride catalyzed reductive Claisen rearrangement reaction was investigated for improvement of diastereoselectivity. The poor diastereoselectivity was ascribed to an undesirable E / Z… (more)

Subjects/Keywords: Boron compounds; Reduction (Chemistry); Copper compounds; Claisen rearrangement

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APA (6th Edition):

Ng, W. (2016). Studies on the copper hydride mediated reductive Claisen rearrangement & synthesis and synthetic applications of C- boron enolates. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/238348

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):

Ng, Wang-hei. “Studies on the copper hydride mediated reductive Claisen rearrangement & synthesis and synthetic applications of C- boron enolates.” 2016. Thesis, University of Hong Kong. Accessed July 13, 2020. http://hdl.handle.net/10722/238348.

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

MLA Handbook (7th Edition):

Ng, Wang-hei. “Studies on the copper hydride mediated reductive Claisen rearrangement & synthesis and synthetic applications of C- boron enolates.” 2016. Web. 13 Jul 2020.

Vancouver:

Ng W. Studies on the copper hydride mediated reductive Claisen rearrangement & synthesis and synthetic applications of C- boron enolates. [Internet] [Thesis]. University of Hong Kong; 2016. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/10722/238348.

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

Council of Science Editors:

Ng W. Studies on the copper hydride mediated reductive Claisen rearrangement & synthesis and synthetic applications of C- boron enolates. [Thesis]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/238348

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


Uniwersytet im. Adama Mickiewicza w Poznaniu

27. Tomas-Szwaczyk, Magdalena. Przegrupowanie Eschenmoser’a-Claisen’a jako metoda otrzymywania α-trifluorometylowych pochodnych kwasów karboksylowych .

Degree: 2011, Uniwersytet im. Adama Mickiewicza w Poznaniu

 Synteza α-trifluorometylowych pochodnych kwasów karboksylowych jest ważnym zagadnieniem w chemii fluoroorganicznej. Reakcja fluorowanych i niefluorowanych alkoholi allilowych z adduktem dietyloaminy z 1,1,3,3,3-pentafluoropropenu (PFPDEA) w obecności… (more)

Subjects/Keywords: przegrupowanie Eschenmoser’a-Claisen’a; eschenmoser-Claisen rearrangement; addukt PFPDEA; PFPDEA adduct; amid kwasu α-trifluorometylowego; α-trifluoromethyl carboxylic acid derivatives

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APA (6th Edition):

Tomas-Szwaczyk, M. (2011). Przegrupowanie Eschenmoser’a-Claisen’a jako metoda otrzymywania α-trifluorometylowych pochodnych kwasów karboksylowych . (Doctoral Dissertation). Uniwersytet im. Adama Mickiewicza w Poznaniu. Retrieved from http://hdl.handle.net/10593/1290

Chicago Manual of Style (16th Edition):

Tomas-Szwaczyk, Magdalena. “Przegrupowanie Eschenmoser’a-Claisen’a jako metoda otrzymywania α-trifluorometylowych pochodnych kwasów karboksylowych .” 2011. Doctoral Dissertation, Uniwersytet im. Adama Mickiewicza w Poznaniu. Accessed July 13, 2020. http://hdl.handle.net/10593/1290.

MLA Handbook (7th Edition):

Tomas-Szwaczyk, Magdalena. “Przegrupowanie Eschenmoser’a-Claisen’a jako metoda otrzymywania α-trifluorometylowych pochodnych kwasów karboksylowych .” 2011. Web. 13 Jul 2020.

Vancouver:

Tomas-Szwaczyk M. Przegrupowanie Eschenmoser’a-Claisen’a jako metoda otrzymywania α-trifluorometylowych pochodnych kwasów karboksylowych . [Internet] [Doctoral dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2011. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/10593/1290.

Council of Science Editors:

Tomas-Szwaczyk M. Przegrupowanie Eschenmoser’a-Claisen’a jako metoda otrzymywania α-trifluorometylowych pochodnych kwasów karboksylowych . [Doctoral Dissertation]. Uniwersytet im. Adama Mickiewicza w Poznaniu; 2011. Available from: http://hdl.handle.net/10593/1290


Indian Institute of Science

28. Ravikumar, P C. Synthetic Approaches To Herbertenoid And Cuparenoid Sesquiterpenes.

Degree: 2006, Indian Institute of Science

 Among Nature's creation, terpenoids are more versatile and exciting natural products. In a remarkable display of synthetic ingenuity and creativity, nature has endowed terpenes with… (more)

Subjects/Keywords: Cuparenoid Sesquiterpenes; Herbertenoid Sesquiterpenes; Natural Products - Synthesis; Olefin Metathesis; Claisen Rearrangement; Herbertenol - Synthesis; Herbertenone - Synthesis; Lagopodin - Synthesis; (±)-lagopodin A; Phytopathogenic Fungus; HM-1; HM-2; Sesquiterpenes; Organic Chemistry

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APA (6th Edition):

Ravikumar, P. C. (2006). Synthetic Approaches To Herbertenoid And Cuparenoid Sesquiterpenes. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/1083

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):

Ravikumar, P C. “Synthetic Approaches To Herbertenoid And Cuparenoid Sesquiterpenes.” 2006. Thesis, Indian Institute of Science. Accessed July 13, 2020. http://hdl.handle.net/2005/1083.

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

MLA Handbook (7th Edition):

Ravikumar, P C. “Synthetic Approaches To Herbertenoid And Cuparenoid Sesquiterpenes.” 2006. Web. 13 Jul 2020.

Vancouver:

Ravikumar PC. Synthetic Approaches To Herbertenoid And Cuparenoid Sesquiterpenes. [Internet] [Thesis]. Indian Institute of Science; 2006. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/2005/1083.

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

Council of Science Editors:

Ravikumar PC. Synthetic Approaches To Herbertenoid And Cuparenoid Sesquiterpenes. [Thesis]. Indian Institute of Science; 2006. Available from: http://hdl.handle.net/2005/1083

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

29. NG KHIM HUI. Synthesis and application of stereoisomeric coordination compounds.

Degree: 2004, National University of Singapore

Subjects/Keywords: cyclopalladated-amine; catalysts; asymmetric Claisen rearrangement; chiral template; asymmetric Diels-Alder; cycloadduct

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APA (6th Edition):

HUI, N. K. (2004). Synthesis and application of stereoisomeric coordination compounds. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/13746

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):

HUI, NG KHIM. “Synthesis and application of stereoisomeric coordination compounds.” 2004. Thesis, National University of Singapore. Accessed July 13, 2020. http://scholarbank.nus.edu.sg/handle/10635/13746.

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

MLA Handbook (7th Edition):

HUI, NG KHIM. “Synthesis and application of stereoisomeric coordination compounds.” 2004. Web. 13 Jul 2020.

Vancouver:

HUI NK. Synthesis and application of stereoisomeric coordination compounds. [Internet] [Thesis]. National University of Singapore; 2004. [cited 2020 Jul 13]. Available from: http://scholarbank.nus.edu.sg/handle/10635/13746.

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

Council of Science Editors:

HUI NK. Synthesis and application of stereoisomeric coordination compounds. [Thesis]. National University of Singapore; 2004. Available from: http://scholarbank.nus.edu.sg/handle/10635/13746

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

30. Zhang, Minhao. The Total Synthesis of () 7-HDHA.

Degree: MSc -MS, Chemistry, 2020, York University

 Fatty acid () 7-HDHA was recently identified as an endogenous ligand for PPAR/ receptors by one of our collaborators Dr. Henry Krause group. While this… (more)

Subjects/Keywords: Molecular chemistry; 7-HDHA; Fatty acid; Total synthesis; ppar; P2-Nickel; Natural product; rcm; Ring-closing metathesis; Hydroxyl docosahexaenoic acid; Semi-hydrogenation; Sonogashira; Claisen rearrangement

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APA (6th Edition):

Zhang, M. (2020). The Total Synthesis of () 7-HDHA. (Masters Thesis). York University. Retrieved from https://yorkspace.library.yorku.ca/xmlui/handle/10315/37385

Chicago Manual of Style (16th Edition):

Zhang, Minhao. “The Total Synthesis of () 7-HDHA.” 2020. Masters Thesis, York University. Accessed July 13, 2020. https://yorkspace.library.yorku.ca/xmlui/handle/10315/37385.

MLA Handbook (7th Edition):

Zhang, Minhao. “The Total Synthesis of () 7-HDHA.” 2020. Web. 13 Jul 2020.

Vancouver:

Zhang M. The Total Synthesis of () 7-HDHA. [Internet] [Masters thesis]. York University; 2020. [cited 2020 Jul 13]. Available from: https://yorkspace.library.yorku.ca/xmlui/handle/10315/37385.

Council of Science Editors:

Zhang M. The Total Synthesis of () 7-HDHA. [Masters Thesis]. York University; 2020. Available from: https://yorkspace.library.yorku.ca/xmlui/handle/10315/37385

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