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You searched for subject:(Prins cyclization). Showing records 1 – 9 of 9 total matches.

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University of New Mexico

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

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 September 20, 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. 20 Sep 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 Sep 20]. 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

2. Durel, Vianney. Développements méthodologiques de la cyclisation d’aza-Prins et aminolyse de lactone pour la synthèse de nouvelles structures peptidomimétiques- pipéridines : Methodological developments in aza-Prins cyclization and lactone aminolysis for the synthesis of piperidine-peptidomimetic scaffolds.

Degree: Docteur es, Chimie, 2016, Rennes 1

Les tétrahydropyranes et les pipéridines sont des motifs que l'on retrouve dans de nombreuses molécules naturelles bioactives. L'intérêt pour ces familles de composés ne cesse… (more)

Subjects/Keywords: Pipéridine; Cyclisation d'aza-Prins; Synthèse diastéréosélective; Effet synergétique; Aminolyse de lactone; Piperidine; Aza-Prins cyclization; Diastereoselective synthesis; Synergistic effect; Lactone aminolysis

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APA (6th Edition):

Durel, V. (2016). Développements méthodologiques de la cyclisation d’aza-Prins et aminolyse de lactone pour la synthèse de nouvelles structures peptidomimétiques- pipéridines : Methodological developments in aza-Prins cyclization and lactone aminolysis for the synthesis of piperidine-peptidomimetic scaffolds. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2016REN1S100

Chicago Manual of Style (16th Edition):

Durel, Vianney. “Développements méthodologiques de la cyclisation d’aza-Prins et aminolyse de lactone pour la synthèse de nouvelles structures peptidomimétiques- pipéridines : Methodological developments in aza-Prins cyclization and lactone aminolysis for the synthesis of piperidine-peptidomimetic scaffolds.” 2016. Doctoral Dissertation, Rennes 1. Accessed September 20, 2020. http://www.theses.fr/2016REN1S100.

MLA Handbook (7th Edition):

Durel, Vianney. “Développements méthodologiques de la cyclisation d’aza-Prins et aminolyse de lactone pour la synthèse de nouvelles structures peptidomimétiques- pipéridines : Methodological developments in aza-Prins cyclization and lactone aminolysis for the synthesis of piperidine-peptidomimetic scaffolds.” 2016. Web. 20 Sep 2020.

Vancouver:

Durel V. Développements méthodologiques de la cyclisation d’aza-Prins et aminolyse de lactone pour la synthèse de nouvelles structures peptidomimétiques- pipéridines : Methodological developments in aza-Prins cyclization and lactone aminolysis for the synthesis of piperidine-peptidomimetic scaffolds. [Internet] [Doctoral dissertation]. Rennes 1; 2016. [cited 2020 Sep 20]. Available from: http://www.theses.fr/2016REN1S100.

Council of Science Editors:

Durel V. Développements méthodologiques de la cyclisation d’aza-Prins et aminolyse de lactone pour la synthèse de nouvelles structures peptidomimétiques- pipéridines : Methodological developments in aza-Prins cyclization and lactone aminolysis for the synthesis of piperidine-peptidomimetic scaffolds. [Doctoral Dissertation]. Rennes 1; 2016. Available from: http://www.theses.fr/2016REN1S100


University of California – Irvine

3. Tay, Gidget C. The Silyl Enol Ether Prins Cyclization: Application to the Total Synthesis of Cyanolide A, Synthesis of Quinolizidine and Indolizidine Heterocycles Using Intramolecular 
Aza-Diels–Alder Reactions, and
 DanceChemistry: A Visual Teaching Aid.

Degree: Chemistry, 2015, University of California – Irvine

 A modular synthesis of the reportedly potent molluscicide, cyanolide A, was developed to provide facile access to a series of cyanolide A analogues. The synthesis… (more)

Subjects/Keywords: Organic chemistry; Chemical education; Diels Alder; Heterocycle methodology; Prins Cyclization; Total synthesis

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APA (6th Edition):

Tay, G. C. (2015). The Silyl Enol Ether Prins Cyclization: Application to the Total Synthesis of Cyanolide A, Synthesis of Quinolizidine and Indolizidine Heterocycles Using Intramolecular 
Aza-Diels–Alder Reactions, and
 DanceChemistry: A Visual Teaching Aid. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/78b3m6k1

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):

Tay, Gidget C. “The Silyl Enol Ether Prins Cyclization: Application to the Total Synthesis of Cyanolide A, Synthesis of Quinolizidine and Indolizidine Heterocycles Using Intramolecular 
Aza-Diels–Alder Reactions, and
 DanceChemistry: A Visual Teaching Aid.” 2015. Thesis, University of California – Irvine. Accessed September 20, 2020. http://www.escholarship.org/uc/item/78b3m6k1.

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

MLA Handbook (7th Edition):

Tay, Gidget C. “The Silyl Enol Ether Prins Cyclization: Application to the Total Synthesis of Cyanolide A, Synthesis of Quinolizidine and Indolizidine Heterocycles Using Intramolecular 
Aza-Diels–Alder Reactions, and
 DanceChemistry: A Visual Teaching Aid.” 2015. Web. 20 Sep 2020.

Vancouver:

Tay GC. The Silyl Enol Ether Prins Cyclization: Application to the Total Synthesis of Cyanolide A, Synthesis of Quinolizidine and Indolizidine Heterocycles Using Intramolecular 
Aza-Diels–Alder Reactions, and
 DanceChemistry: A Visual Teaching Aid. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2020 Sep 20]. Available from: http://www.escholarship.org/uc/item/78b3m6k1.

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

Council of Science Editors:

Tay GC. The Silyl Enol Ether Prins Cyclization: Application to the Total Synthesis of Cyanolide A, Synthesis of Quinolizidine and Indolizidine Heterocycles Using Intramolecular 
Aza-Diels–Alder Reactions, and
 DanceChemistry: A Visual Teaching Aid. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/78b3m6k1

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

4. Saulo Luis Capim. Síntese diastereosseletivas e atividades antinociceptivas de novos derivados tetraidropirânicos substituídos.

Degree: 2013, Universidade Federal da Paraíba

Neste trabalho, é descrito a síntese de 10 novos derivados tetraidropirânicos compostos (42 51) planejados a partir da estrutura do ()-Naproxeno, utilizando a reação de… (more)

Subjects/Keywords: Atividade antinociceptiva; Ciclização de Prins; Química orgânica; Derivados tetraidropirânicos; Hibridização molecular; Química medicinal; QUIMICA; Prins cyclization reaction; antinociceptive activity; tetrahydropiran derivatives; molecular hybridization; Medicinal chemistry

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APA (6th Edition):

Capim, S. L. (2013). Síntese diastereosseletivas e atividades antinociceptivas de novos derivados tetraidropirânicos substituídos. (Thesis). Universidade Federal da Paraíba. Retrieved from http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=2829

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):

Capim, Saulo Luis. “Síntese diastereosseletivas e atividades antinociceptivas de novos derivados tetraidropirânicos substituídos.” 2013. Thesis, Universidade Federal da Paraíba. Accessed September 20, 2020. http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=2829.

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

MLA Handbook (7th Edition):

Capim, Saulo Luis. “Síntese diastereosseletivas e atividades antinociceptivas de novos derivados tetraidropirânicos substituídos.” 2013. Web. 20 Sep 2020.

Vancouver:

Capim SL. Síntese diastereosseletivas e atividades antinociceptivas de novos derivados tetraidropirânicos substituídos. [Internet] [Thesis]. Universidade Federal da Paraíba; 2013. [cited 2020 Sep 20]. Available from: http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=2829.

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

Council of Science Editors:

Capim SL. Síntese diastereosseletivas e atividades antinociceptivas de novos derivados tetraidropirânicos substituídos. [Thesis]. Universidade Federal da Paraíba; 2013. Available from: http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=2829

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

5. Fábio Pedrosa Lins Silva. Reação de ciclização de prins na síntetica diastereosseletiva de 31 análogos meso-tetraidropirâneos: determinação de estruturas cristalinas, estudos teóricos e avaliação in vitro da atividade antileucêmica.

Degree: 2013, Universidade Federal da Paraíba

Este trabalho foi idealizado baseado no conceito de compostos aquirais/meso. A importância da preparação de compostos aquirais está baseada na sua simplificação estrutural, conduzindo a… (more)

Subjects/Keywords: Química; Tetraidropiranos aquirais/meso; Ciclização de prins; QUIMICA ORGANICA; Tetrahydropyran achiral/meso; Barbier reaction; Prins cyclization reaction; Tetrahydropyranyl derivatives; Diastereoselective synthesis; Crystal structures determination; DFT; Cancer

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

APA (6th Edition):

Silva, F. P. L. (2013). Reação de ciclização de prins na síntetica diastereosseletiva de 31 análogos meso-tetraidropirâneos: determinação de estruturas cristalinas, estudos teóricos e avaliação in vitro da atividade antileucêmica. (Thesis). Universidade Federal da Paraíba. Retrieved from http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=2845

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):

Silva, Fábio Pedrosa Lins. “Reação de ciclização de prins na síntetica diastereosseletiva de 31 análogos meso-tetraidropirâneos: determinação de estruturas cristalinas, estudos teóricos e avaliação in vitro da atividade antileucêmica.” 2013. Thesis, Universidade Federal da Paraíba. Accessed September 20, 2020. http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=2845.

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

MLA Handbook (7th Edition):

Silva, Fábio Pedrosa Lins. “Reação de ciclização de prins na síntetica diastereosseletiva de 31 análogos meso-tetraidropirâneos: determinação de estruturas cristalinas, estudos teóricos e avaliação in vitro da atividade antileucêmica.” 2013. Web. 20 Sep 2020.

Vancouver:

Silva FPL. Reação de ciclização de prins na síntetica diastereosseletiva de 31 análogos meso-tetraidropirâneos: determinação de estruturas cristalinas, estudos teóricos e avaliação in vitro da atividade antileucêmica. [Internet] [Thesis]. Universidade Federal da Paraíba; 2013. [cited 2020 Sep 20]. Available from: http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=2845.

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

Council of Science Editors:

Silva FPL. Reação de ciclização de prins na síntetica diastereosseletiva de 31 análogos meso-tetraidropirâneos: determinação de estruturas cristalinas, estudos teóricos e avaliação in vitro da atividade antileucêmica. [Thesis]. Universidade Federal da Paraíba; 2013. Available from: http://bdtd.biblioteca.ufpb.br/tde_busca/arquivo.php?codArquivo=2845

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

6. Quintiliano, Samir Augusto Pino. Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina.

Degree: PhD, Química Orgânica, 2010, University of São Paulo

Abordaram-se diversos aspectos da reação de contração de álcoois homoalílicos promovida por trinitrato de tálio (TTN). A configuração relativa do indano obtido como produto foi… (more)

Subjects/Keywords: Carambola (pesquisa); Caramboxin; Caramboxina; Ciclização de Prins; Contração de anel; Hypervalent iodine; Iodine; Iodo; Iodo hipervalente; Organic reactions; Organic synthesis; Prins cyclization; Reações orgânicas; Ring contraction; Síntese orgânica; Thallium trinitrate; Toxinas; Toxins; Trinitrato de tálio

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APA (6th Edition):

Quintiliano, S. A. P. (2010). Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-27042010-082909/ ;

Chicago Manual of Style (16th Edition):

Quintiliano, Samir Augusto Pino. “Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina.” 2010. Doctoral Dissertation, University of São Paulo. Accessed September 20, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-27042010-082909/ ;.

MLA Handbook (7th Edition):

Quintiliano, Samir Augusto Pino. “Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina.” 2010. Web. 20 Sep 2020.

Vancouver:

Quintiliano SAP. Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Sep 20]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-27042010-082909/ ;.

Council of Science Editors:

Quintiliano SAP. Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-27042010-082909/ ;

7. Jacolot, Maïwenn. Vers la synthèse totale du portentol et de la stachybotrine C : Toward the total synthesis of portentol and stachybotrin C.

Degree: Docteur es, Chimie, 2013, Rennes 1

Le portentol est un polypropionate qui possède une structure spirocyclique très originale. Cette molécule, dont il n'existe encore aucune synthèse totale, a été isolée du… (more)

Subjects/Keywords: Portentol; Polypropionate; Cyclisation de Prins; Spirotétrahydropyrane; Dédoublement cinétique dynamique; Synthèse totale; Chimie médicinale; Stachybotrine C; Hydroarylation par catalyse à l’or; Époxydation/cyclisation.; Portentol; Polypropionate; Prins cyclization; Spirotetrahydropyrane; Dynamic kinetic resolution; Total synthesis; Medicinal chemistry; Stachybotrin C; Gold-catalyzed hydroarylation; Epoxydation/cyclisation.

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APA (6th Edition):

Jacolot, M. (2013). Vers la synthèse totale du portentol et de la stachybotrine C : Toward the total synthesis of portentol and stachybotrin C. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2013REN1S129

Chicago Manual of Style (16th Edition):

Jacolot, Maïwenn. “Vers la synthèse totale du portentol et de la stachybotrine C : Toward the total synthesis of portentol and stachybotrin C.” 2013. Doctoral Dissertation, Rennes 1. Accessed September 20, 2020. http://www.theses.fr/2013REN1S129.

MLA Handbook (7th Edition):

Jacolot, Maïwenn. “Vers la synthèse totale du portentol et de la stachybotrine C : Toward the total synthesis of portentol and stachybotrin C.” 2013. Web. 20 Sep 2020.

Vancouver:

Jacolot M. Vers la synthèse totale du portentol et de la stachybotrine C : Toward the total synthesis of portentol and stachybotrin C. [Internet] [Doctoral dissertation]. Rennes 1; 2013. [cited 2020 Sep 20]. Available from: http://www.theses.fr/2013REN1S129.

Council of Science Editors:

Jacolot M. Vers la synthèse totale du portentol et de la stachybotrine C : Toward the total synthesis of portentol and stachybotrin C. [Doctoral Dissertation]. Rennes 1; 2013. Available from: http://www.theses.fr/2013REN1S129

8. LEE CHENG HSIA, ANGELINE. Development of new methodologies for the synthesis of enantiomerically enriched compounds.

Degree: 2006, National University of Singapore

Subjects/Keywords: Homoallylic alcohols; Allyl transfer; Tandem reactions; olefin metathesis; Prins cyclization

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APA (6th Edition):

LEE CHENG HSIA, A. (2006). Development of new methodologies for the synthesis of enantiomerically enriched compounds. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/15073

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

Chicago Manual of Style (16th Edition):

LEE CHENG HSIA, ANGELINE. “Development of new methodologies for the synthesis of enantiomerically enriched compounds.” 2006. Thesis, National University of Singapore. Accessed September 20, 2020. http://scholarbank.nus.edu.sg/handle/10635/15073.

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

MLA Handbook (7th Edition):

LEE CHENG HSIA, ANGELINE. “Development of new methodologies for the synthesis of enantiomerically enriched compounds.” 2006. Web. 20 Sep 2020.

Vancouver:

LEE CHENG HSIA A. Development of new methodologies for the synthesis of enantiomerically enriched compounds. [Internet] [Thesis]. National University of Singapore; 2006. [cited 2020 Sep 20]. Available from: http://scholarbank.nus.edu.sg/handle/10635/15073.

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

Council of Science Editors:

LEE CHENG HSIA A. Development of new methodologies for the synthesis of enantiomerically enriched compounds. [Thesis]. National University of Singapore; 2006. Available from: http://scholarbank.nus.edu.sg/handle/10635/15073

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


The Ohio State University

9. Figueroa, Ruth. Application of the prins cyclization to a synthesis of the tetrahydropyran rings of lasonolide A.

Degree: PhD, Chemistry, 2004, The Ohio State University

 This thesis describes studies toward the synthesis of the tetrahydropyran-containing marine macrolide lasonolide A. A summary of studies done by Lee and coworkers, that led… (more)

Subjects/Keywords: Chemistry, Organic; Lasonolide A; Prins cyclization; Vinylogous carbonate; enol ether; asymmetric synthesis

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APA (6th Edition):

Figueroa, R. (2004). Application of the prins cyclization to a synthesis of the tetrahydropyran rings of lasonolide A. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1098890473

Chicago Manual of Style (16th Edition):

Figueroa, Ruth. “Application of the prins cyclization to a synthesis of the tetrahydropyran rings of lasonolide A.” 2004. Doctoral Dissertation, The Ohio State University. Accessed September 20, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1098890473.

MLA Handbook (7th Edition):

Figueroa, Ruth. “Application of the prins cyclization to a synthesis of the tetrahydropyran rings of lasonolide A.” 2004. Web. 20 Sep 2020.

Vancouver:

Figueroa R. Application of the prins cyclization to a synthesis of the tetrahydropyran rings of lasonolide A. [Internet] [Doctoral dissertation]. The Ohio State University; 2004. [cited 2020 Sep 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1098890473.

Council of Science Editors:

Figueroa R. Application of the prins cyclization to a synthesis of the tetrahydropyran rings of lasonolide A. [Doctoral Dissertation]. The Ohio State University; 2004. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1098890473

.