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You searched for subject:(marine natural product). Showing records 1 – 22 of 22 total matches.

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NSYSU

1. Hsieh, Chi-hua. Studies on the Natural Products of the Formosan Soft Coral Sinularia sp.

Degree: Master, Marine Resources, 2005, NSYSU

 The chemical constituents of EtOH extracts of the soft coral Sinularia sp. have led to the isolation of nature compoundsï¼1-12ï¼,sinularioperoxides A-Dï¼1-4ï¼, sinulariolins A-Dï¼5-8ï¼, 1a,3b-Dihydroxy-24-methylencholesta-5,9-dieneï¼9ï¼,ï¼3Sï¼-3,7-Dimethyl-nona- 6,8-dienoicacidï¼10ï¼,… (more)

Subjects/Keywords: marine; natural product

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

APA (6th Edition):

Hsieh, C. (2005). Studies on the Natural Products of the Formosan Soft Coral Sinularia sp. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816105-233855

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):

Hsieh, Chi-hua. “Studies on the Natural Products of the Formosan Soft Coral Sinularia sp.” 2005. Thesis, NSYSU. Accessed November 23, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816105-233855.

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

MLA Handbook (7th Edition):

Hsieh, Chi-hua. “Studies on the Natural Products of the Formosan Soft Coral Sinularia sp.” 2005. Web. 23 Nov 2020.

Vancouver:

Hsieh C. Studies on the Natural Products of the Formosan Soft Coral Sinularia sp. [Internet] [Thesis]. NSYSU; 2005. [cited 2020 Nov 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816105-233855.

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

Council of Science Editors:

Hsieh C. Studies on the Natural Products of the Formosan Soft Coral Sinularia sp. [Thesis]. NSYSU; 2005. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0816105-233855

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


University of the Western Cape

2. Lerata, Mookho Sylvia. Discovery of cytotoxic natural products from South African marine sponges .

Degree: 2018, University of the Western Cape

 Cancer is a major health problem worldwide and killing millions of people each year. The use of natural products as chemotherapeutic agents is well established,… (more)

Subjects/Keywords: Cancer; marine sponges; Ircinia sp.; Latrunculid sp. Pyrroloiminoquinones alkaloids; furanosesterterpenes; cytotoxicity; marine natural product libraries.

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APA (6th Edition):

Lerata, M. S. (2018). Discovery of cytotoxic natural products from South African marine sponges . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/6447

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):

Lerata, Mookho Sylvia. “Discovery of cytotoxic natural products from South African marine sponges .” 2018. Thesis, University of the Western Cape. Accessed November 23, 2020. http://hdl.handle.net/11394/6447.

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

MLA Handbook (7th Edition):

Lerata, Mookho Sylvia. “Discovery of cytotoxic natural products from South African marine sponges .” 2018. Web. 23 Nov 2020.

Vancouver:

Lerata MS. Discovery of cytotoxic natural products from South African marine sponges . [Internet] [Thesis]. University of the Western Cape; 2018. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/11394/6447.

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

Council of Science Editors:

Lerata MS. Discovery of cytotoxic natural products from South African marine sponges . [Thesis]. University of the Western Cape; 2018. Available from: http://hdl.handle.net/11394/6447

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


NSYSU

3. Lin, Chun-kuang. Development of antiviral drugs from marine natural products and investigation of drug target against virus.

Degree: PhD, Doctoral Degree Program in Marine Biotechnology, 2018, NSYSU

 Hepatitis C virus (HCV) infection causes chronic inflammation of liver, leading to the development of cirrhosis and hepatocellular carcinoma (HCC). Infection of dengue virus (DENV)… (more)

Subjects/Keywords: DENV; COX-2; marine natural product; EGFR; prostasin; HCV

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APA (6th Edition):

Lin, C. (2018). Development of antiviral drugs from marine natural products and investigation of drug target against virus. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0019118-192352

Chicago Manual of Style (16th Edition):

Lin, Chun-kuang. “Development of antiviral drugs from marine natural products and investigation of drug target against virus.” 2018. Doctoral Dissertation, NSYSU. Accessed November 23, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0019118-192352.

MLA Handbook (7th Edition):

Lin, Chun-kuang. “Development of antiviral drugs from marine natural products and investigation of drug target against virus.” 2018. Web. 23 Nov 2020.

Vancouver:

Lin C. Development of antiviral drugs from marine natural products and investigation of drug target against virus. [Internet] [Doctoral dissertation]. NSYSU; 2018. [cited 2020 Nov 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0019118-192352.

Council of Science Editors:

Lin C. Development of antiviral drugs from marine natural products and investigation of drug target against virus. [Doctoral Dissertation]. NSYSU; 2018. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0019118-192352


University of Waikato

4. Wang, Alice Tansi. Elucidating the Modes of Action of the Antitumour New Zealand Marine Natural Product Pterocellin A .

Degree: 2015, University of Waikato

 Pterocellin A is a novel bioactive alkaloid isolated from the New Zealand marine bryozoan Pterocella vesiculosa. It exhibits potent antitumour activity towards the P388 (murine… (more)

Subjects/Keywords: natural product; apoptosis; bryozoan; cell death; marine; biochemistry; chemistry

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APA (6th Edition):

Wang, A. T. (2015). Elucidating the Modes of Action of the Antitumour New Zealand Marine Natural Product Pterocellin A . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/9620

Chicago Manual of Style (16th Edition):

Wang, Alice Tansi. “Elucidating the Modes of Action of the Antitumour New Zealand Marine Natural Product Pterocellin A .” 2015. Masters Thesis, University of Waikato. Accessed November 23, 2020. http://hdl.handle.net/10289/9620.

MLA Handbook (7th Edition):

Wang, Alice Tansi. “Elucidating the Modes of Action of the Antitumour New Zealand Marine Natural Product Pterocellin A .” 2015. Web. 23 Nov 2020.

Vancouver:

Wang AT. Elucidating the Modes of Action of the Antitumour New Zealand Marine Natural Product Pterocellin A . [Internet] [Masters thesis]. University of Waikato; 2015. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/10289/9620.

Council of Science Editors:

Wang AT. Elucidating the Modes of Action of the Antitumour New Zealand Marine Natural Product Pterocellin A . [Masters Thesis]. University of Waikato; 2015. Available from: http://hdl.handle.net/10289/9620


University of the Western Cape

5. Elbagory, Abdulrahman Mohammed. Chemical and biological evaluation of palythoa tuberculosa collected from the red sea .

Degree: 2015, University of the Western Cape

 A chemical study on the total extract of the zoanthid Palythoa tuberculosa, collected from the Red Sea, resulted in the isolation of seven polyhydroxylated sterols… (more)

Subjects/Keywords: Marine natural product; Red Sea; Palythoa tuberculosa; Polyhydroxylated sterols; Cytotoxicity; Apoptosis

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APA (6th Edition):

Elbagory, A. M. (2015). Chemical and biological evaluation of palythoa tuberculosa collected from the red sea . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4107

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):

Elbagory, Abdulrahman Mohammed. “Chemical and biological evaluation of palythoa tuberculosa collected from the red sea .” 2015. Thesis, University of the Western Cape. Accessed November 23, 2020. http://hdl.handle.net/11394/4107.

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

MLA Handbook (7th Edition):

Elbagory, Abdulrahman Mohammed. “Chemical and biological evaluation of palythoa tuberculosa collected from the red sea .” 2015. Web. 23 Nov 2020.

Vancouver:

Elbagory AM. Chemical and biological evaluation of palythoa tuberculosa collected from the red sea . [Internet] [Thesis]. University of the Western Cape; 2015. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/11394/4107.

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

Council of Science Editors:

Elbagory AM. Chemical and biological evaluation of palythoa tuberculosa collected from the red sea . [Thesis]. University of the Western Cape; 2015. Available from: http://hdl.handle.net/11394/4107

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


Victoria University of Wellington

6. Turupadang, Wem. Revisiting marine bioprospecting of tropical Indonesian macroalgae from West Timor.

Degree: 2018, Victoria University of Wellington

Marine algae are an important and historically rich source of new marine-based natural products. This thesis describes the screening of 40 Indonesian macroalgal samples using… (more)

Subjects/Keywords: Marine macroalgae; Global Natural Product Social Molecular Networking; Timor; GNPS; Indonesia

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APA (6th Edition):

Turupadang, W. (2018). Revisiting marine bioprospecting of tropical Indonesian macroalgae from West Timor. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/8290

Chicago Manual of Style (16th Edition):

Turupadang, Wem. “Revisiting marine bioprospecting of tropical Indonesian macroalgae from West Timor.” 2018. Masters Thesis, Victoria University of Wellington. Accessed November 23, 2020. http://hdl.handle.net/10063/8290.

MLA Handbook (7th Edition):

Turupadang, Wem. “Revisiting marine bioprospecting of tropical Indonesian macroalgae from West Timor.” 2018. Web. 23 Nov 2020.

Vancouver:

Turupadang W. Revisiting marine bioprospecting of tropical Indonesian macroalgae from West Timor. [Internet] [Masters thesis]. Victoria University of Wellington; 2018. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/10063/8290.

Council of Science Editors:

Turupadang W. Revisiting marine bioprospecting of tropical Indonesian macroalgae from West Timor. [Masters Thesis]. Victoria University of Wellington; 2018. Available from: http://hdl.handle.net/10063/8290


University of Cambridge

7. Yip, Adam Christopher Loy. Studies towards the total synthesis of madeirolide A.

Degree: PhD, 2018, University of Cambridge

 Madeirolide A (1) is a structurally novel polyketide natural product first isolated from the deep-sea sponge Leiodermatium sp. by Wright in 2009. Initial biological investigations… (more)

Subjects/Keywords: organic chemistry; natural products; total synthesis; marine natural product; polyketide; macrocycle; anti-fungal; madeirolide

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APA (6th Edition):

Yip, A. C. L. (2018). Studies towards the total synthesis of madeirolide A. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.32287 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763672

Chicago Manual of Style (16th Edition):

Yip, Adam Christopher Loy. “Studies towards the total synthesis of madeirolide A.” 2018. Doctoral Dissertation, University of Cambridge. Accessed November 23, 2020. https://doi.org/10.17863/CAM.32287 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763672.

MLA Handbook (7th Edition):

Yip, Adam Christopher Loy. “Studies towards the total synthesis of madeirolide A.” 2018. Web. 23 Nov 2020.

Vancouver:

Yip ACL. Studies towards the total synthesis of madeirolide A. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2020 Nov 23]. Available from: https://doi.org/10.17863/CAM.32287 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763672.

Council of Science Editors:

Yip ACL. Studies towards the total synthesis of madeirolide A. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://doi.org/10.17863/CAM.32287 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763672


NSYSU

8. Cheng, Yuan-Bin. Studies on the Natural Products from the Taiwanese Soft Corals Clavularia viridis, Xenia florida, Cespitularia taeniata, Cespitularia hypotentaculata, and Sarcophyton stolidotum.

Degree: PhD, Marine Biotechnology and Resources, 2007, NSYSU

 This dissertation mainly discussed the investigation of five different soft corals collected in Green Island and one soft coral collected in Kenting. They were identified… (more)

Subjects/Keywords: cytotoxicity; diterpenoid; marine natural product; prostanoid

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APA (6th Edition):

Cheng, Y. (2007). Studies on the Natural Products from the Taiwanese Soft Corals Clavularia viridis, Xenia florida, Cespitularia taeniata, Cespitularia hypotentaculata, and Sarcophyton stolidotum. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0716107-112739

Chicago Manual of Style (16th Edition):

Cheng, Yuan-Bin. “Studies on the Natural Products from the Taiwanese Soft Corals Clavularia viridis, Xenia florida, Cespitularia taeniata, Cespitularia hypotentaculata, and Sarcophyton stolidotum.” 2007. Doctoral Dissertation, NSYSU. Accessed November 23, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0716107-112739.

MLA Handbook (7th Edition):

Cheng, Yuan-Bin. “Studies on the Natural Products from the Taiwanese Soft Corals Clavularia viridis, Xenia florida, Cespitularia taeniata, Cespitularia hypotentaculata, and Sarcophyton stolidotum.” 2007. Web. 23 Nov 2020.

Vancouver:

Cheng Y. Studies on the Natural Products from the Taiwanese Soft Corals Clavularia viridis, Xenia florida, Cespitularia taeniata, Cespitularia hypotentaculata, and Sarcophyton stolidotum. [Internet] [Doctoral dissertation]. NSYSU; 2007. [cited 2020 Nov 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0716107-112739.

Council of Science Editors:

Cheng Y. Studies on the Natural Products from the Taiwanese Soft Corals Clavularia viridis, Xenia florida, Cespitularia taeniata, Cespitularia hypotentaculata, and Sarcophyton stolidotum. [Doctoral Dissertation]. NSYSU; 2007. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0716107-112739

9. Solanki, Hiren Keshavlal. Chemical diversity of some benthic cyanobacteria from French Polynesia and New Caledonia.

Degree: 2020, NUI Galway

 Cyanobacteria are often considered proliferative in relation with the global change affecting oceans worldwide and especially in the coral reefs of the Pacific Ocean. The… (more)

Subjects/Keywords: Marine Natural Product Chemistry; Chemistry; Science; Chemical diversity; benthic cyanobacteria; French Polynesia; New Caledonia

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APA (6th Edition):

Solanki, H. K. (2020). Chemical diversity of some benthic cyanobacteria from French Polynesia and New Caledonia. (Thesis). NUI Galway. Retrieved from http://hdl.handle.net/10379/16117

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):

Solanki, Hiren Keshavlal. “Chemical diversity of some benthic cyanobacteria from French Polynesia and New Caledonia.” 2020. Thesis, NUI Galway. Accessed November 23, 2020. http://hdl.handle.net/10379/16117.

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

MLA Handbook (7th Edition):

Solanki, Hiren Keshavlal. “Chemical diversity of some benthic cyanobacteria from French Polynesia and New Caledonia.” 2020. Web. 23 Nov 2020.

Vancouver:

Solanki HK. Chemical diversity of some benthic cyanobacteria from French Polynesia and New Caledonia. [Internet] [Thesis]. NUI Galway; 2020. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/10379/16117.

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

Council of Science Editors:

Solanki HK. Chemical diversity of some benthic cyanobacteria from French Polynesia and New Caledonia. [Thesis]. NUI Galway; 2020. Available from: http://hdl.handle.net/10379/16117

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


NSYSU

10. Cheng, Po-yi. Study on the Chemical Constituents of Marine-Derived Fungus, Fusarium solani and Their Biological Activities.; Study on the Synthesis of Vitroprocines and Its Derivatives.

Degree: Master, Marine Biotechnology and Resources, 2016, NSYSU

 Part 1 When searching the novel anti-microbial secondary metabolites from marine-derived fungus. We found a symbiotic fungus, Fusarium solani (FS-01), isolated from a Palythoa sp.,… (more)

Subjects/Keywords: marine fungus; Fusarium solani; Bacillus cereus; cytotoxicity; oral cancer; natural product; amino-polyketide derivatives; antibiotics; marine Vibrio sp.

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APA (6th Edition):

Cheng, P. (2016). Study on the Chemical Constituents of Marine-Derived Fungus, Fusarium solani and Their Biological Activities.; Study on the Synthesis of Vitroprocines and Its Derivatives. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0724116-095035

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):

Cheng, Po-yi. “Study on the Chemical Constituents of Marine-Derived Fungus, Fusarium solani and Their Biological Activities.; Study on the Synthesis of Vitroprocines and Its Derivatives.” 2016. Thesis, NSYSU. Accessed November 23, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0724116-095035.

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

MLA Handbook (7th Edition):

Cheng, Po-yi. “Study on the Chemical Constituents of Marine-Derived Fungus, Fusarium solani and Their Biological Activities.; Study on the Synthesis of Vitroprocines and Its Derivatives.” 2016. Web. 23 Nov 2020.

Vancouver:

Cheng P. Study on the Chemical Constituents of Marine-Derived Fungus, Fusarium solani and Their Biological Activities.; Study on the Synthesis of Vitroprocines and Its Derivatives. [Internet] [Thesis]. NSYSU; 2016. [cited 2020 Nov 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0724116-095035.

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

Council of Science Editors:

Cheng P. Study on the Chemical Constituents of Marine-Derived Fungus, Fusarium solani and Their Biological Activities.; Study on the Synthesis of Vitroprocines and Its Derivatives. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0724116-095035

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


NSYSU

11. Chen, Chun-Hong. The therapeutic effects of coral-compound and PTEN in rats with traumatic spinal cord injury.

Degree: PhD, Doctoral Degree Program in Marine Biotechnology, 2016, NSYSU

 In the present study intrathecal pretreatment 11-dehydrosinulariolide attenuated spinal cord injury (SCI)-induced cell apoptosis by upregulating the antiapoptotic protein Bcl-2 and cell survival-related pathway proteins… (more)

Subjects/Keywords: microglia; marine natural product; 11-dehydrosinulariolide; neuroprotection; spinal cord injury; anti-inflammation; phosphatase and tensin homologue deleted on chromosome 10; astrocyte; glial scar; chondroitin sulfate proteoglycans

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APA (6th Edition):

Chen, C. (2016). The therapeutic effects of coral-compound and PTEN in rats with traumatic spinal cord injury. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0730114-150126

Chicago Manual of Style (16th Edition):

Chen, Chun-Hong. “The therapeutic effects of coral-compound and PTEN in rats with traumatic spinal cord injury.” 2016. Doctoral Dissertation, NSYSU. Accessed November 23, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0730114-150126.

MLA Handbook (7th Edition):

Chen, Chun-Hong. “The therapeutic effects of coral-compound and PTEN in rats with traumatic spinal cord injury.” 2016. Web. 23 Nov 2020.

Vancouver:

Chen C. The therapeutic effects of coral-compound and PTEN in rats with traumatic spinal cord injury. [Internet] [Doctoral dissertation]. NSYSU; 2016. [cited 2020 Nov 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0730114-150126.

Council of Science Editors:

Chen C. The therapeutic effects of coral-compound and PTEN in rats with traumatic spinal cord injury. [Doctoral Dissertation]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0730114-150126


University of Queensland

12. Forster, Louise. Insights into the chemical composition and ecology of nudibranchs of the genus Goniobranchus.

Degree: School of Chemistry and Molecular Biosciences, 2020, University of Queensland

Subjects/Keywords: Nudibranch; Goniobranchus; Diterpenes; Molecular modelling; NMR; Marine natural product; Stereochemistry; 0305 Organic Chemistry

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APA (6th Edition):

Forster, L. (2020). Insights into the chemical composition and ecology of nudibranchs of the genus Goniobranchus. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:38

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):

Forster, Louise. “Insights into the chemical composition and ecology of nudibranchs of the genus Goniobranchus.” 2020. Thesis, University of Queensland. Accessed November 23, 2020. http://espace.library.uq.edu.au/view/UQ:38.

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

MLA Handbook (7th Edition):

Forster, Louise. “Insights into the chemical composition and ecology of nudibranchs of the genus Goniobranchus.” 2020. Web. 23 Nov 2020.

Vancouver:

Forster L. Insights into the chemical composition and ecology of nudibranchs of the genus Goniobranchus. [Internet] [Thesis]. University of Queensland; 2020. [cited 2020 Nov 23]. Available from: http://espace.library.uq.edu.au/view/UQ:38.

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

Council of Science Editors:

Forster L. Insights into the chemical composition and ecology of nudibranchs of the genus Goniobranchus. [Thesis]. University of Queensland; 2020. Available from: http://espace.library.uq.edu.au/view/UQ:38

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

13. Alqahtani, Norah Faihan. Synergizing Microbial Culturing, Whole Genome Sequencing, Asymmetric Synthesis and Tandem MS for Reconstruction of Polyketide and Alkaloid Natural Product Biosynthesis in Marine Actinomycete Nocardiopsis sp CMB- M0232.

Degree: PhD, Chemistry, 2015, Case Western Reserve University School of Graduate Studies

 Biosynthetic pathway engineering is rapidly growing by rationally harnessing the enzymatic potential of microbial systems. While marine cyanobacterial genus and a few gram positive bacteria… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Biochemistry; Asymmetric,Synthesis,Biosynthesis,Marine Natural Product,Polyketide,Alkaloid,Nocardiopsin,Nocardioazine,Actinomycete Nocardiopsis sp CMBM0232,Tandem MS,Microbial Culturing, Genome Sequencing

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APA (6th Edition):

Alqahtani, N. F. (2015). Synergizing Microbial Culturing, Whole Genome Sequencing, Asymmetric Synthesis and Tandem MS for Reconstruction of Polyketide and Alkaloid Natural Product Biosynthesis in Marine Actinomycete Nocardiopsis sp CMB- M0232. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1421167765

Chicago Manual of Style (16th Edition):

Alqahtani, Norah Faihan. “Synergizing Microbial Culturing, Whole Genome Sequencing, Asymmetric Synthesis and Tandem MS for Reconstruction of Polyketide and Alkaloid Natural Product Biosynthesis in Marine Actinomycete Nocardiopsis sp CMB- M0232.” 2015. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed November 23, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1421167765.

MLA Handbook (7th Edition):

Alqahtani, Norah Faihan. “Synergizing Microbial Culturing, Whole Genome Sequencing, Asymmetric Synthesis and Tandem MS for Reconstruction of Polyketide and Alkaloid Natural Product Biosynthesis in Marine Actinomycete Nocardiopsis sp CMB- M0232.” 2015. Web. 23 Nov 2020.

Vancouver:

Alqahtani NF. Synergizing Microbial Culturing, Whole Genome Sequencing, Asymmetric Synthesis and Tandem MS for Reconstruction of Polyketide and Alkaloid Natural Product Biosynthesis in Marine Actinomycete Nocardiopsis sp CMB- M0232. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2015. [cited 2020 Nov 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1421167765.

Council of Science Editors:

Alqahtani NF. Synergizing Microbial Culturing, Whole Genome Sequencing, Asymmetric Synthesis and Tandem MS for Reconstruction of Polyketide and Alkaloid Natural Product Biosynthesis in Marine Actinomycete Nocardiopsis sp CMB- M0232. [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1421167765


Université Paris-Sud – Paris XI

14. Rambla, Matt. Synthèse totale du 13-desméthyle spirolide C : Total synthesis of 13-desmethyl spirolide C.

Degree: Docteur es, Chimie, 2015, Université Paris-Sud – Paris XI

Les gymnodimines, les spirolides, les pinnatoxines et les ptériatoxines constituent une famille de toxines d’origine marine de structures complexes, produites en faibles quantités par des… (more)

Subjects/Keywords: Spirolide; Spiroimine; Toxine marine; Produit naturel; Récepteurs nicotiniques; Synthèse asymétrique; Catalyse; Palladium; Allylation décarboxylante asymétrique; Isomerisation; Cycloaddition; Spirolide; Spiroimine; Marine toxin; Natural product; Nicotinic receptor; Asymmetric synthesis; Catalysis; Palladium; Asymmetric decarboxylative allylation; Isomerization; Cycloaddition

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APA (6th Edition):

Rambla, M. (2015). Synthèse totale du 13-desméthyle spirolide C : Total synthesis of 13-desmethyl spirolide C. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA112169

Chicago Manual of Style (16th Edition):

Rambla, Matt. “Synthèse totale du 13-desméthyle spirolide C : Total synthesis of 13-desmethyl spirolide C.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed November 23, 2020. http://www.theses.fr/2015PA112169.

MLA Handbook (7th Edition):

Rambla, Matt. “Synthèse totale du 13-desméthyle spirolide C : Total synthesis of 13-desmethyl spirolide C.” 2015. Web. 23 Nov 2020.

Vancouver:

Rambla M. Synthèse totale du 13-desméthyle spirolide C : Total synthesis of 13-desmethyl spirolide C. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2020 Nov 23]. Available from: http://www.theses.fr/2015PA112169.

Council of Science Editors:

Rambla M. Synthèse totale du 13-desméthyle spirolide C : Total synthesis of 13-desmethyl spirolide C. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA112169


Université Paris-Sud – Paris XI

15. Duroure, Leslie. Vers la synthèse de la (-) - gymnodimine A et études de relations structure-activité du coeur spiroimine : Toward the total synthesis of the (−)-gymnodimine A and relations between structure and activity of the spiroimine moiety.

Degree: Docteur es, Chimie organique, 2011, Université Paris-Sud – Paris XI

Les gymnodimines, les spirolides, les pinatoxines et les ptériatoxines constituent une famille de toxines d’origine marine de structures complexes, produites en faibles quantités par des… (more)

Subjects/Keywords: Gymnodimine; Spiroimine; Toxine marine; Produit naturel; Récepteurs nicotiniques; Synthèse asymmétrique; Catalyse; Palladium; Allylation décarboxylante asymétrique; Cycloaddition; Réaction de Tsuji-Trost; Gymnodimine; Spiroimine; Marine toxine; Natural product; Nicotinic receptor; Asymmetric synthesis; Catalysis; Palladium; Decarboxylative asymetric allylation; Cycloaddition; Tsuji-Trost reaction

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

APA (6th Edition):

Duroure, L. (2011). Vers la synthèse de la (-) - gymnodimine A et études de relations structure-activité du coeur spiroimine : Toward the total synthesis of the (−)-gymnodimine A and relations between structure and activity of the spiroimine moiety. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA112206

Chicago Manual of Style (16th Edition):

Duroure, Leslie. “Vers la synthèse de la (-) - gymnodimine A et études de relations structure-activité du coeur spiroimine : Toward the total synthesis of the (−)-gymnodimine A and relations between structure and activity of the spiroimine moiety.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed November 23, 2020. http://www.theses.fr/2011PA112206.

MLA Handbook (7th Edition):

Duroure, Leslie. “Vers la synthèse de la (-) - gymnodimine A et études de relations structure-activité du coeur spiroimine : Toward the total synthesis of the (−)-gymnodimine A and relations between structure and activity of the spiroimine moiety.” 2011. Web. 23 Nov 2020.

Vancouver:

Duroure L. Vers la synthèse de la (-) - gymnodimine A et études de relations structure-activité du coeur spiroimine : Toward the total synthesis of the (−)-gymnodimine A and relations between structure and activity of the spiroimine moiety. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2020 Nov 23]. Available from: http://www.theses.fr/2011PA112206.

Council of Science Editors:

Duroure L. Vers la synthèse de la (-) - gymnodimine A et études de relations structure-activité du coeur spiroimine : Toward the total synthesis of the (−)-gymnodimine A and relations between structure and activity of the spiroimine moiety. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA112206


Universitetet i Tromsø

16. Mishchenko, Ekaterina. Antibacterial and anti-biofilm activity of novel marine natural product mimics .

Degree: 2017, Universitetet i Tromsø

 Infectious diseases represent an urgent public health problem globally. Particularly healthcare-associated infections are often complicated by antibiotic resistance and presence of recalcitrant microbial biofilms. On… (more)

Subjects/Keywords: VDP::Technology: 500::Biotechnology: 590; Marine bioprospecting; VDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Medical microbiology: 715; anti-biofilm; marine natural product mimics; mechanism of action; Staphylococcus epidermidis; RP62A; membrane-active; ESBL–CARBA; antimicrobial; drug discovery; antibiotic resistance; antibacterial

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

APA (6th Edition):

Mishchenko, E. (2017). Antibacterial and anti-biofilm activity of novel marine natural product mimics . (Doctoral Dissertation). Universitetet i Tromsø. Retrieved from http://hdl.handle.net/10037/12105

Chicago Manual of Style (16th Edition):

Mishchenko, Ekaterina. “Antibacterial and anti-biofilm activity of novel marine natural product mimics .” 2017. Doctoral Dissertation, Universitetet i Tromsø. Accessed November 23, 2020. http://hdl.handle.net/10037/12105.

MLA Handbook (7th Edition):

Mishchenko, Ekaterina. “Antibacterial and anti-biofilm activity of novel marine natural product mimics .” 2017. Web. 23 Nov 2020.

Vancouver:

Mishchenko E. Antibacterial and anti-biofilm activity of novel marine natural product mimics . [Internet] [Doctoral dissertation]. Universitetet i Tromsø 2017. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/10037/12105.

Council of Science Editors:

Mishchenko E. Antibacterial and anti-biofilm activity of novel marine natural product mimics . [Doctoral Dissertation]. Universitetet i Tromsø 2017. Available from: http://hdl.handle.net/10037/12105


Université Paris-Sud – Paris XI

17. Jusseau, Xavier. Etudes sur la synthèse du coeur spiroimine de la (–)-gymnodimine A et réaction d'addition asymétrique de silyloxyfuranes sur des accepteurs de Michael cycliques : Toward the synthesis of the spiroimine core of (-)-gymnodimine A and enantioselective addition of silyoxyfurans to cyclic Michael acceptors.

Degree: Docteur es, Chimie organique, 2013, Université Paris-Sud – Paris XI

Les gymnodimines, les spirolides, les pinnatoxines et les ptériatoxines constituent une famille de toxines d’origine marine de structures complexes, produites en faibles quantités par des… (more)

Subjects/Keywords: Gymnodimine; Spiroimine; Toxine marine; Produit naturel; Récepteurs nicotiniques; Réaction de Mukaiyama-Michael; Synthèse asymmétrique; Catalyse au cuivre; Complexe bis(oxazoline); Buténolide; Silyloxyfurane; Β-cétoesters cycliques; Gymnodimine; Spiroimine; Marine toxine; Natural product; Nicotinic receptor; Mukaiyama-Michael reaction; Asymmetric synthesis; Copper catalysis; Bis(oxazoline) complex; Butenolide; Silyloxyfuran; Cyclic β-ketoesters

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

APA (6th Edition):

Jusseau, X. (2013). Etudes sur la synthèse du coeur spiroimine de la (–)-gymnodimine A et réaction d'addition asymétrique de silyloxyfuranes sur des accepteurs de Michael cycliques : Toward the synthesis of the spiroimine core of (-)-gymnodimine A and enantioselective addition of silyoxyfurans to cyclic Michael acceptors. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA112283

Chicago Manual of Style (16th Edition):

Jusseau, Xavier. “Etudes sur la synthèse du coeur spiroimine de la (–)-gymnodimine A et réaction d'addition asymétrique de silyloxyfuranes sur des accepteurs de Michael cycliques : Toward the synthesis of the spiroimine core of (-)-gymnodimine A and enantioselective addition of silyoxyfurans to cyclic Michael acceptors.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed November 23, 2020. http://www.theses.fr/2013PA112283.

MLA Handbook (7th Edition):

Jusseau, Xavier. “Etudes sur la synthèse du coeur spiroimine de la (–)-gymnodimine A et réaction d'addition asymétrique de silyloxyfuranes sur des accepteurs de Michael cycliques : Toward the synthesis of the spiroimine core of (-)-gymnodimine A and enantioselective addition of silyoxyfurans to cyclic Michael acceptors.” 2013. Web. 23 Nov 2020.

Vancouver:

Jusseau X. Etudes sur la synthèse du coeur spiroimine de la (–)-gymnodimine A et réaction d'addition asymétrique de silyloxyfuranes sur des accepteurs de Michael cycliques : Toward the synthesis of the spiroimine core of (-)-gymnodimine A and enantioselective addition of silyoxyfurans to cyclic Michael acceptors. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2020 Nov 23]. Available from: http://www.theses.fr/2013PA112283.

Council of Science Editors:

Jusseau X. Etudes sur la synthèse du coeur spiroimine de la (–)-gymnodimine A et réaction d'addition asymétrique de silyloxyfuranes sur des accepteurs de Michael cycliques : Toward the synthesis of the spiroimine core of (-)-gymnodimine A and enantioselective addition of silyoxyfurans to cyclic Michael acceptors. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA112283


University of Florida

18. Cai, Weijing. Drug Discovery and Development of Natural Products from Marine Cyanobacteria as Anticancer Agents and Growth Factor Modulators.

Degree: PhD, Pharmaceutical Sciences - Medicinal Chemistry, 2017, University of Florida

Subjects/Keywords: antiangiogenesis; anticancer; antiproliferative; apratoxins; cytotoxic; growth-factors; marine-cyanobacteria; mechanism-of-action; natural-product

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APA (6th Edition):

Cai, W. (2017). Drug Discovery and Development of Natural Products from Marine Cyanobacteria as Anticancer Agents and Growth Factor Modulators. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0051438

Chicago Manual of Style (16th Edition):

Cai, Weijing. “Drug Discovery and Development of Natural Products from Marine Cyanobacteria as Anticancer Agents and Growth Factor Modulators.” 2017. Doctoral Dissertation, University of Florida. Accessed November 23, 2020. https://ufdc.ufl.edu/UFE0051438.

MLA Handbook (7th Edition):

Cai, Weijing. “Drug Discovery and Development of Natural Products from Marine Cyanobacteria as Anticancer Agents and Growth Factor Modulators.” 2017. Web. 23 Nov 2020.

Vancouver:

Cai W. Drug Discovery and Development of Natural Products from Marine Cyanobacteria as Anticancer Agents and Growth Factor Modulators. [Internet] [Doctoral dissertation]. University of Florida; 2017. [cited 2020 Nov 23]. Available from: https://ufdc.ufl.edu/UFE0051438.

Council of Science Editors:

Cai W. Drug Discovery and Development of Natural Products from Marine Cyanobacteria as Anticancer Agents and Growth Factor Modulators. [Doctoral Dissertation]. University of Florida; 2017. Available from: https://ufdc.ufl.edu/UFE0051438

19. Lane, Amy L. Marine natural products as antimicrobial chemical defenses and sources of potential drugs.

Degree: PhD, Chemistry and Biochemistry, 2008, Georgia Tech

Marine organisms are widely recognized sources of an impressive array of structurally unusual compounds. Marine natural products have exhibited interesting biomedical activities, provided targets for… (more)

Subjects/Keywords: Chemical defense; Natural product; Chemical ecology; Shikimate; Terpenoid; NMR; DESI-MS; Algae; Antimicrobial; Drug discovery; Marine; Marine natural products; Pharmacognosy; Anti-infective agents

marine natural product studies are young relative to terrestrial investigations, biomedically… …motivated marine natural product studies have already yielded structurally novel compounds with… …biosynthesis. The following chapters represent combined explorations of marine natural product… …Northcote, P. T., and Prinsep, M. R. (2007). Marine natural products. Natural Product… …Prinsep, M. R. (2008). Marine natural products. Natural Product Reports 25, 35-94… 

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APA (6th Edition):

Lane, A. L. (2008). Marine natural products as antimicrobial chemical defenses and sources of potential drugs. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26556

Chicago Manual of Style (16th Edition):

Lane, Amy L. “Marine natural products as antimicrobial chemical defenses and sources of potential drugs.” 2008. Doctoral Dissertation, Georgia Tech. Accessed November 23, 2020. http://hdl.handle.net/1853/26556.

MLA Handbook (7th Edition):

Lane, Amy L. “Marine natural products as antimicrobial chemical defenses and sources of potential drugs.” 2008. Web. 23 Nov 2020.

Vancouver:

Lane AL. Marine natural products as antimicrobial chemical defenses and sources of potential drugs. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/1853/26556.

Council of Science Editors:

Lane AL. Marine natural products as antimicrobial chemical defenses and sources of potential drugs. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/26556

20. Westley, Chantel Barbara. The distribution, biosynthetic origin and functional significance of Tyrian purple precursors in the Australian muricid Dicathais orbita (Neogastropoda: Muricidae).

Degree: 2008, Flinders University

 Information on the biosynthetic origin and functional advantage of marine mollusc natural products is not only essential to our understanding of chemical ecology, but to… (more)

Subjects/Keywords: Muricidae; Neogastropoda; Tyrian purple; marine natural product; de novo biosynthesis; bromoperoxidase; arylsulphatase; tyrindoxyl sulphate; hypobranchial gland; gonoduct; egg capsule; ingesting gland; albumen gland; seminal receptacle; sperm storage; larval chemical defence

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APA (6th Edition):

Westley, C. B. (2008). The distribution, biosynthetic origin and functional significance of Tyrian purple precursors in the Australian muricid Dicathais orbita (Neogastropoda: Muricidae). (Thesis). Flinders University. Retrieved from http://catalogue.flinders.edu.au./local/adt/public/adt-SFU20090414.153942

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):

Westley, Chantel Barbara. “The distribution, biosynthetic origin and functional significance of Tyrian purple precursors in the Australian muricid Dicathais orbita (Neogastropoda: Muricidae).” 2008. Thesis, Flinders University. Accessed November 23, 2020. http://catalogue.flinders.edu.au./local/adt/public/adt-SFU20090414.153942.

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

MLA Handbook (7th Edition):

Westley, Chantel Barbara. “The distribution, biosynthetic origin and functional significance of Tyrian purple precursors in the Australian muricid Dicathais orbita (Neogastropoda: Muricidae).” 2008. Web. 23 Nov 2020.

Vancouver:

Westley CB. The distribution, biosynthetic origin and functional significance of Tyrian purple precursors in the Australian muricid Dicathais orbita (Neogastropoda: Muricidae). [Internet] [Thesis]. Flinders University; 2008. [cited 2020 Nov 23]. Available from: http://catalogue.flinders.edu.au./local/adt/public/adt-SFU20090414.153942.

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

Council of Science Editors:

Westley CB. The distribution, biosynthetic origin and functional significance of Tyrian purple precursors in the Australian muricid Dicathais orbita (Neogastropoda: Muricidae). [Thesis]. Flinders University; 2008. Available from: http://catalogue.flinders.edu.au./local/adt/public/adt-SFU20090414.153942

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

21. Hähnel-Linker, Manuela. Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester.

Degree: 2002, Universität Dortmund

Das Ziel des ersten Projektes war die Darstellung eines enantiomer einheitlichen Synthese-bausteins auf der Basis von Tris(hydroxymethyl)ethan. Über eine enzymkatalysierte Vereste-rung mit Chirazyme-L2 und Vinylacetat… (more)

Subjects/Keywords: C-20-Epimerisierung; C-20-Epimerization; chiral building block; Chiraler Synthesebaustein; configurational assignment; Desymmetrisierung von Tris(hydroxymethyl)ethan; desymmetrization of tris(hydroxymethyl)ethan; enzyme-catalized transesterification; Enzymkatalysierte Veresterung; Konfigurationsbestimmung; marine natural product; Mariner Naturstoff; 540

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APA (6th Edition):

Hähnel-Linker, M. (2002). Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester. (Thesis). Universität Dortmund. Retrieved from http://hdl.handle.net/2003/2487

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):

Hähnel-Linker, Manuela. “Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester.” 2002. Thesis, Universität Dortmund. Accessed November 23, 2020. http://hdl.handle.net/2003/2487.

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

MLA Handbook (7th Edition):

Hähnel-Linker, Manuela. “Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester.” 2002. Web. 23 Nov 2020.

Vancouver:

Hähnel-Linker M. Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester. [Internet] [Thesis]. Universität Dortmund; 2002. [cited 2020 Nov 23]. Available from: http://hdl.handle.net/2003/2487.

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

Council of Science Editors:

Hähnel-Linker M. Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester. [Thesis]. Universität Dortmund; 2002. Available from: http://hdl.handle.net/2003/2487

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

22. Hähnel-Linker, Manuela. Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester.

Degree: 2002, Technische Universität Dortmund

 In a first project, a chiral building block, based on a tris(hydroxymethyl)ethane-derivative should be prepared. An enzyme-catalyzed transesterification, using Chirazyme-L2 and vinyl acetate led to… (more)

Subjects/Keywords: Chiraler Synthesebaustein; Enzymkatalysierte Veresterung; Desymmetrisierung von Tris(hydroxymethyl)ethan; Mariner Naturstoff; C-20-Epimerisierung; Konfigurationsbestimmung; chiral building block; enzyme-catalized transesterification; desymmetrization of tris(hydroxymethyl)ethan; marine natural product; C-20-Epimerization; configurational assignment; 540

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

APA (6th Edition):

Hähnel-Linker, M. (2002). Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-14853

Chicago Manual of Style (16th Edition):

Hähnel-Linker, Manuela. “Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester.” 2002. Doctoral Dissertation, Technische Universität Dortmund. Accessed November 23, 2020. http://dx.doi.org/10.17877/DE290R-14853.

MLA Handbook (7th Edition):

Hähnel-Linker, Manuela. “Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester.” 2002. Web. 23 Nov 2020.

Vancouver:

Hähnel-Linker M. Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2002. [cited 2020 Nov 23]. Available from: http://dx.doi.org/10.17877/DE290R-14853.

Council of Science Editors:

Hähnel-Linker M. Enantiomerenreine Tris(hydroxymethyl)ethan-Derivate als chirale Synthesebausteine und Synthese von (20R,22E)- und (20S,22E)-3-Oxochola-1,4,22-trien-24-säuremethylester. [Doctoral Dissertation]. Technische Universität Dortmund; 2002. Available from: http://dx.doi.org/10.17877/DE290R-14853

.