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You searched for subject:(Boronic acids). Showing records 1 – 30 of 32 total matches.

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University of Edinburgh

1. Cox, Paul Alan. Protodeboronation.

Degree: PhD, 2017, University of Edinburgh

Boronic acids are key reagents in a host of chemical applications. In particular, they have been utilised in a range of metal-catalysed coupling reactions, involving… (more)

Subjects/Keywords: 547; boronic acids; protodeboronation

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APA (6th Edition):

Cox, P. A. (2017). Protodeboronation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25383

Chicago Manual of Style (16th Edition):

Cox, Paul Alan. “Protodeboronation.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed July 18, 2019. http://hdl.handle.net/1842/25383.

MLA Handbook (7th Edition):

Cox, Paul Alan. “Protodeboronation.” 2017. Web. 18 Jul 2019.

Vancouver:

Cox PA. Protodeboronation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/1842/25383.

Council of Science Editors:

Cox PA. Protodeboronation. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/25383


Georgia State University

2. Laughlin, Sarah R. Arylboronic Acids With Strong Fluorescence Intensity Changes Upon Sugar Binding.

Degree: MS, Chemistry, 2011, Georgia State University

Boronic acids play an important role in the design and synthesis of chemosensors for carbohydrates due to their ability to reversibly bind with diol-containing… (more)

Subjects/Keywords: Chemosensor; Boronic acids; Saccharide recognition; Isoquinoline-7-boronic acid; Phenoxathiin-4-boronic acid; Fluorescence spectroscopy

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APA (6th Edition):

Laughlin, S. R. (2011). Arylboronic Acids With Strong Fluorescence Intensity Changes Upon Sugar Binding. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/46

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):

Laughlin, Sarah R. “Arylboronic Acids With Strong Fluorescence Intensity Changes Upon Sugar Binding.” 2011. Thesis, Georgia State University. Accessed July 18, 2019. https://scholarworks.gsu.edu/chemistry_theses/46.

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

MLA Handbook (7th Edition):

Laughlin, Sarah R. “Arylboronic Acids With Strong Fluorescence Intensity Changes Upon Sugar Binding.” 2011. Web. 18 Jul 2019.

Vancouver:

Laughlin SR. Arylboronic Acids With Strong Fluorescence Intensity Changes Upon Sugar Binding. [Internet] [Thesis]. Georgia State University; 2011. [cited 2019 Jul 18]. Available from: https://scholarworks.gsu.edu/chemistry_theses/46.

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

Council of Science Editors:

Laughlin SR. Arylboronic Acids With Strong Fluorescence Intensity Changes Upon Sugar Binding. [Thesis]. Georgia State University; 2011. Available from: https://scholarworks.gsu.edu/chemistry_theses/46

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

3. Reverte, Maëva. Etude de la biocompatibilité d acides nucléiques modifiés par des acides boroniques : développement de nouveaux outils de diagnostic : Study of the biocompatibility of nucleic acid modified by boronic acid : development to new diagnostic tools.

Degree: Docteur es, Ingénierie moléculaire, 2016, Montpellier

La modification d’oligonucléotides est un domaine attrayant de la chimie organique. De nombreuses études se sont intéressées à la génération de liens internucléosidiques artificiels à… (more)

Subjects/Keywords: Acides nucléiques; Acides boroniques; Biocompatibilité; Nucleic acids; Boronic acids; Biocompatibility

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APA (6th Edition):

Reverte, M. (2016). Etude de la biocompatibilité d acides nucléiques modifiés par des acides boroniques : développement de nouveaux outils de diagnostic : Study of the biocompatibility of nucleic acid modified by boronic acid : development to new diagnostic tools. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2016MONTT236

Chicago Manual of Style (16th Edition):

Reverte, Maëva. “Etude de la biocompatibilité d acides nucléiques modifiés par des acides boroniques : développement de nouveaux outils de diagnostic : Study of the biocompatibility of nucleic acid modified by boronic acid : development to new diagnostic tools.” 2016. Doctoral Dissertation, Montpellier. Accessed July 18, 2019. http://www.theses.fr/2016MONTT236.

MLA Handbook (7th Edition):

Reverte, Maëva. “Etude de la biocompatibilité d acides nucléiques modifiés par des acides boroniques : développement de nouveaux outils de diagnostic : Study of the biocompatibility of nucleic acid modified by boronic acid : development to new diagnostic tools.” 2016. Web. 18 Jul 2019.

Vancouver:

Reverte M. Etude de la biocompatibilité d acides nucléiques modifiés par des acides boroniques : développement de nouveaux outils de diagnostic : Study of the biocompatibility of nucleic acid modified by boronic acid : development to new diagnostic tools. [Internet] [Doctoral dissertation]. Montpellier; 2016. [cited 2019 Jul 18]. Available from: http://www.theses.fr/2016MONTT236.

Council of Science Editors:

Reverte M. Etude de la biocompatibilité d acides nucléiques modifiés par des acides boroniques : développement de nouveaux outils de diagnostic : Study of the biocompatibility of nucleic acid modified by boronic acid : development to new diagnostic tools. [Doctoral Dissertation]. Montpellier; 2016. Available from: http://www.theses.fr/2016MONTT236


University of Manchester

4. Brown, James Robert David. Boronate-diol interactions in membranes : a biomimetic tool for polysaccharide recognition.

Degree: PhD, 2013, University of Manchester

 Molecular recognition at biomembranes is one of the more poorly understood aspects of fundamental research in physical organic chemistry. Our aim was to improve our… (more)

Subjects/Keywords: 547; Boronic acids; Saccharides; Molecular Recognition; Biomembranes; Ionophore; Ion Transport

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APA (6th Edition):

Brown, J. R. D. (2013). Boronate-diol interactions in membranes : a biomimetic tool for polysaccharide recognition. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/boronatediol-interactions-in-membranes-a-biomimetic-tool-for-polysaccharide-recognition(8a625ef7-0149-4be3-862f-b8be00f4942d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570287

Chicago Manual of Style (16th Edition):

Brown, James Robert David. “Boronate-diol interactions in membranes : a biomimetic tool for polysaccharide recognition.” 2013. Doctoral Dissertation, University of Manchester. Accessed July 18, 2019. https://www.research.manchester.ac.uk/portal/en/theses/boronatediol-interactions-in-membranes-a-biomimetic-tool-for-polysaccharide-recognition(8a625ef7-0149-4be3-862f-b8be00f4942d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570287.

MLA Handbook (7th Edition):

Brown, James Robert David. “Boronate-diol interactions in membranes : a biomimetic tool for polysaccharide recognition.” 2013. Web. 18 Jul 2019.

Vancouver:

Brown JRD. Boronate-diol interactions in membranes : a biomimetic tool for polysaccharide recognition. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Jul 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/boronatediol-interactions-in-membranes-a-biomimetic-tool-for-polysaccharide-recognition(8a625ef7-0149-4be3-862f-b8be00f4942d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570287.

Council of Science Editors:

Brown JRD. Boronate-diol interactions in membranes : a biomimetic tool for polysaccharide recognition. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/boronatediol-interactions-in-membranes-a-biomimetic-tool-for-polysaccharide-recognition(8a625ef7-0149-4be3-862f-b8be00f4942d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.570287


University of California – Santa Cruz

5. Resendez, Angel. Beyond Glucose Recognition: Development of a Multiwell Assay for the Recognition of Sugars and Sugar Derivatives as GI Permeability Markers.

Degree: Chemistry, 2017, University of California – Santa Cruz

 Gastrointestinal barrier dysfunction is now recognized as an early event in the pathogenesis of several problematic diseases, such as inflammatory bowel disease (IBD), Parkinson’s disease,… (more)

Subjects/Keywords: Chemistry; Arrays; Assay Development; Boronic Acids; Gastrointestinal; Lactulose; Permeability

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APA (6th Edition):

Resendez, A. (2017). Beyond Glucose Recognition: Development of a Multiwell Assay for the Recognition of Sugars and Sugar Derivatives as GI Permeability Markers. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/8t60s08s

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):

Resendez, Angel. “Beyond Glucose Recognition: Development of a Multiwell Assay for the Recognition of Sugars and Sugar Derivatives as GI Permeability Markers.” 2017. Thesis, University of California – Santa Cruz. Accessed July 18, 2019. http://www.escholarship.org/uc/item/8t60s08s.

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

MLA Handbook (7th Edition):

Resendez, Angel. “Beyond Glucose Recognition: Development of a Multiwell Assay for the Recognition of Sugars and Sugar Derivatives as GI Permeability Markers.” 2017. Web. 18 Jul 2019.

Vancouver:

Resendez A. Beyond Glucose Recognition: Development of a Multiwell Assay for the Recognition of Sugars and Sugar Derivatives as GI Permeability Markers. [Internet] [Thesis]. University of California – Santa Cruz; 2017. [cited 2019 Jul 18]. Available from: http://www.escholarship.org/uc/item/8t60s08s.

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

Council of Science Editors:

Resendez A. Beyond Glucose Recognition: Development of a Multiwell Assay for the Recognition of Sugars and Sugar Derivatives as GI Permeability Markers. [Thesis]. University of California – Santa Cruz; 2017. Available from: http://www.escholarship.org/uc/item/8t60s08s

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


East Tennessee State University

6. Appiah Kubi, George. Functionalization of Silica Surface Using Chan-Lam Coupling.

Degree: MS, Chemistry, 2014, East Tennessee State University

  The reaction of base-free Chan-Lam coupling was successfully used for functionalization of surface of mesoporous silica gel. Various aromatic, aliphatic, and heterocyclic compounds were… (more)

Subjects/Keywords: Chan-Lam coupling; surface functionalization; silica gel; boronic acids; Organic Chemistry

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APA (6th Edition):

Appiah Kubi, G. (2014). Functionalization of Silica Surface Using Chan-Lam Coupling. (Masters Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/2335

Chicago Manual of Style (16th Edition):

Appiah Kubi, George. “Functionalization of Silica Surface Using Chan-Lam Coupling.” 2014. Masters Thesis, East Tennessee State University. Accessed July 18, 2019. https://dc.etsu.edu/etd/2335.

MLA Handbook (7th Edition):

Appiah Kubi, George. “Functionalization of Silica Surface Using Chan-Lam Coupling.” 2014. Web. 18 Jul 2019.

Vancouver:

Appiah Kubi G. Functionalization of Silica Surface Using Chan-Lam Coupling. [Internet] [Masters thesis]. East Tennessee State University; 2014. [cited 2019 Jul 18]. Available from: https://dc.etsu.edu/etd/2335.

Council of Science Editors:

Appiah Kubi G. Functionalization of Silica Surface Using Chan-Lam Coupling. [Masters Thesis]. East Tennessee State University; 2014. Available from: https://dc.etsu.edu/etd/2335


University of Bath

7. Cox, Owen. Chemical modification of polysulfone.

Degree: PhD, 2013, University of Bath

 The research presented herein is concerned with the chemical modification of polysulfone towards the synthesis of a hollow fibre boronic acid fixed carrier membrane system… (more)

Subjects/Keywords: 547; organic chemistry; polymer chemistry; boronic acids; hollow fibre membranes

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APA (6th Edition):

Cox, O. (2013). Chemical modification of polysulfone. (Doctoral Dissertation). University of Bath. Retrieved from https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.665375

Chicago Manual of Style (16th Edition):

Cox, Owen. “Chemical modification of polysulfone.” 2013. Doctoral Dissertation, University of Bath. Accessed July 18, 2019. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.665375.

MLA Handbook (7th Edition):

Cox, Owen. “Chemical modification of polysulfone.” 2013. Web. 18 Jul 2019.

Vancouver:

Cox O. Chemical modification of polysulfone. [Internet] [Doctoral dissertation]. University of Bath; 2013. [cited 2019 Jul 18]. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.665375.

Council of Science Editors:

Cox O. Chemical modification of polysulfone. [Doctoral Dissertation]. University of Bath; 2013. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.665375


University of Manitoba

8. Geary, Laina Michelle. A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene.

Degree: Chemistry, 2011, University of Manitoba

 Trichloroethylene, a simple and very inexpensive material, has been identified as a tri- and tetrafunctionalizable building block. A combination of selective palladium-catalyzed cross-coupling reactions with… (more)

Subjects/Keywords: palladium; heterocycles; direct arylation; cross-coupling; boronic acids; trichloroethylene

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APA (6th Edition):

Geary, L. M. (2011). A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/4381

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):

Geary, Laina Michelle. “A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene.” 2011. Thesis, University of Manitoba. Accessed July 18, 2019. http://hdl.handle.net/1993/4381.

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

MLA Handbook (7th Edition):

Geary, Laina Michelle. “A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene.” 2011. Web. 18 Jul 2019.

Vancouver:

Geary LM. A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene. [Internet] [Thesis]. University of Manitoba; 2011. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/1993/4381.

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

Council of Science Editors:

Geary LM. A diversity-oriented approach to the palladium-catalyzed modular assembly of conjugated compounds and heterocycles: high-value compounds from trichloroethylene. [Thesis]. University of Manitoba; 2011. Available from: http://hdl.handle.net/1993/4381

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


University of Cambridge

9. Lima, Fabio. Photoredox C-C cross-coupling reactions using boronic acid derivatives.

Degree: PhD, 2018, University of Cambridge

 In recent years, photoredox catalysis emerged as a privileged tool for small molecules activation via single-electron transfer mechanisms. Despite their ubiquity as reagents in organic… (more)

Subjects/Keywords: photoredox; catalysis; boronic acids; boronic esters; cross-couplings; synthetic methods; lewis base; flow; visible light; photochemistry

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APA (6th Edition):

Lima, F. (2018). Photoredox C-C cross-coupling reactions using boronic acid derivatives. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274928 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744718

Chicago Manual of Style (16th Edition):

Lima, Fabio. “Photoredox C-C cross-coupling reactions using boronic acid derivatives.” 2018. Doctoral Dissertation, University of Cambridge. Accessed July 18, 2019. https://www.repository.cam.ac.uk/handle/1810/274928 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744718.

MLA Handbook (7th Edition):

Lima, Fabio. “Photoredox C-C cross-coupling reactions using boronic acid derivatives.” 2018. Web. 18 Jul 2019.

Vancouver:

Lima F. Photoredox C-C cross-coupling reactions using boronic acid derivatives. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Jul 18]. Available from: https://www.repository.cam.ac.uk/handle/1810/274928 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744718.

Council of Science Editors:

Lima F. Photoredox C-C cross-coupling reactions using boronic acid derivatives. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274928 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744718


University of Cambridge

10. Lima, Fabio. Photoredox C–C Cross-Coupling Reactions using Boronic Acid Derivatives .

Degree: 2018, University of Cambridge

 In recent years, photoredox catalysis emerged as a privileged tool for small molecules activation via single-electron transfer mechanisms. Despite their ubiquity as reagents in organic… (more)

Subjects/Keywords: photoredox; catalysis; boronic acids; boronic esters; cross-couplings; synthetic methods; lewis base; flow; visible light; photochemistry

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APA (6th Edition):

Lima, F. (2018). Photoredox C–C Cross-Coupling Reactions using Boronic Acid Derivatives . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274928

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):

Lima, Fabio. “Photoredox C–C Cross-Coupling Reactions using Boronic Acid Derivatives .” 2018. Thesis, University of Cambridge. Accessed July 18, 2019. https://www.repository.cam.ac.uk/handle/1810/274928.

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

MLA Handbook (7th Edition):

Lima, Fabio. “Photoredox C–C Cross-Coupling Reactions using Boronic Acid Derivatives .” 2018. Web. 18 Jul 2019.

Vancouver:

Lima F. Photoredox C–C Cross-Coupling Reactions using Boronic Acid Derivatives . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Jul 18]. Available from: https://www.repository.cam.ac.uk/handle/1810/274928.

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

Council of Science Editors:

Lima F. Photoredox C–C Cross-Coupling Reactions using Boronic Acid Derivatives . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274928

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


University of Florida

11. Simocko, Chester Kent. Application of Boron in Olefin Metathesis.

Degree: PhD, Chemistry, 2013, University of Florida

 Controlling polymer morphology is key to controlling andpredicting physical and electronic properties. However, in many cases polymer morphology is unknown because the primarystructure of the polymer… (more)

Subjects/Keywords: Alkenes; Boron; Boronic acids; Catalysts; Lewis acids; Metathesis; Monomers; Polymerization; Polymers; Solvents; acids  – admet  – boron  – catalyst  – metathesis  – olefin  – polymer

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APA (6th Edition):

Simocko, C. K. (2013). Application of Boron in Olefin Metathesis. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0045879

Chicago Manual of Style (16th Edition):

Simocko, Chester Kent. “Application of Boron in Olefin Metathesis.” 2013. Doctoral Dissertation, University of Florida. Accessed July 18, 2019. http://ufdc.ufl.edu/UFE0045879.

MLA Handbook (7th Edition):

Simocko, Chester Kent. “Application of Boron in Olefin Metathesis.” 2013. Web. 18 Jul 2019.

Vancouver:

Simocko CK. Application of Boron in Olefin Metathesis. [Internet] [Doctoral dissertation]. University of Florida; 2013. [cited 2019 Jul 18]. Available from: http://ufdc.ufl.edu/UFE0045879.

Council of Science Editors:

Simocko CK. Application of Boron in Olefin Metathesis. [Doctoral Dissertation]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/UFE0045879


University of Florida

12. Brooks, William L. Investigating Boronic Acid-Diol Binding and the Application of Boronic Acids to Stimuli-Responsive Materials.

Degree: PhD, Chemistry, 2015, University of Florida

 The use of boronic acids has seen significant increase over the last few decades, as researchers have employed the functional group in smart materials ranging… (more)

Subjects/Keywords: Borinic acids; Boronic acids; Esters; Gels; Hydrogels; Monomers; pH; Polymerization; Polymers; Titration; acid  – boronic  – diabetes  – glucose  – polymerization  – raft  – rdrp  – responsive  – stimuli  – thermoresponsive

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APA (6th Edition):

Brooks, W. L. (2015). Investigating Boronic Acid-Diol Binding and the Application of Boronic Acids to Stimuli-Responsive Materials. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0049489

Chicago Manual of Style (16th Edition):

Brooks, William L. “Investigating Boronic Acid-Diol Binding and the Application of Boronic Acids to Stimuli-Responsive Materials.” 2015. Doctoral Dissertation, University of Florida. Accessed July 18, 2019. http://ufdc.ufl.edu/UFE0049489.

MLA Handbook (7th Edition):

Brooks, William L. “Investigating Boronic Acid-Diol Binding and the Application of Boronic Acids to Stimuli-Responsive Materials.” 2015. Web. 18 Jul 2019.

Vancouver:

Brooks WL. Investigating Boronic Acid-Diol Binding and the Application of Boronic Acids to Stimuli-Responsive Materials. [Internet] [Doctoral dissertation]. University of Florida; 2015. [cited 2019 Jul 18]. Available from: http://ufdc.ufl.edu/UFE0049489.

Council of Science Editors:

Brooks WL. Investigating Boronic Acid-Diol Binding and the Application of Boronic Acids to Stimuli-Responsive Materials. [Doctoral Dissertation]. University of Florida; 2015. Available from: http://ufdc.ufl.edu/UFE0049489


Georgia State University

13. Ni, Nanting. Application of Boronic Acids in Medicinal Chemistry (Inhibitors, Sensors).

Degree: PhD, Chemistry, 2010, Georgia State University

  It is well known boronic acids have its unique chemistry and related applications in organic synthesis. The boronic acid functionally group also plays very… (more)

Subjects/Keywords: SPR; Selex; Aptamer; Boronic acids; Sensor; Quorum sensing; Autoinducer-2; Inhibitor; Hydrogen peroxide; Chemistry

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APA (6th Edition):

Ni, N. (2010). Application of Boronic Acids in Medicinal Chemistry (Inhibitors, Sensors). (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/34

Chicago Manual of Style (16th Edition):

Ni, Nanting. “Application of Boronic Acids in Medicinal Chemistry (Inhibitors, Sensors).” 2010. Doctoral Dissertation, Georgia State University. Accessed July 18, 2019. https://scholarworks.gsu.edu/chemistry_diss/34.

MLA Handbook (7th Edition):

Ni, Nanting. “Application of Boronic Acids in Medicinal Chemistry (Inhibitors, Sensors).” 2010. Web. 18 Jul 2019.

Vancouver:

Ni N. Application of Boronic Acids in Medicinal Chemistry (Inhibitors, Sensors). [Internet] [Doctoral dissertation]. Georgia State University; 2010. [cited 2019 Jul 18]. Available from: https://scholarworks.gsu.edu/chemistry_diss/34.

Council of Science Editors:

Ni N. Application of Boronic Acids in Medicinal Chemistry (Inhibitors, Sensors). [Doctoral Dissertation]. Georgia State University; 2010. Available from: https://scholarworks.gsu.edu/chemistry_diss/34


University of Bath

14. Penrose, Stephen David. Recent advances in rhodium-catalysed conjugate addition reactions.

Degree: PhD, 2008, University of Bath

 The research presented herein is concerned with the exploration of rhodium-catalysed addition reactions with organoboranes encompassing the 1,4-addition enolate protonation to benzyl acrylate esters, and… (more)

Subjects/Keywords: 547.6; boronic acids; conjugate addition; rhodium

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APA (6th Edition):

Penrose, S. D. (2008). Recent advances in rhodium-catalysed conjugate addition reactions. (Doctoral Dissertation). University of Bath. Retrieved from https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.492243

Chicago Manual of Style (16th Edition):

Penrose, Stephen David. “Recent advances in rhodium-catalysed conjugate addition reactions.” 2008. Doctoral Dissertation, University of Bath. Accessed July 18, 2019. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.492243.

MLA Handbook (7th Edition):

Penrose, Stephen David. “Recent advances in rhodium-catalysed conjugate addition reactions.” 2008. Web. 18 Jul 2019.

Vancouver:

Penrose SD. Recent advances in rhodium-catalysed conjugate addition reactions. [Internet] [Doctoral dissertation]. University of Bath; 2008. [cited 2019 Jul 18]. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.492243.

Council of Science Editors:

Penrose SD. Recent advances in rhodium-catalysed conjugate addition reactions. [Doctoral Dissertation]. University of Bath; 2008. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.492243


University of Houston

15. Lundy, Brian J. I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY.

Degree: Chemistry, Department of, 2013, University of Houston

 This dissertation presents two different projects, the first being the use of boronic acids in conjugate addition reactions on different substituted indoles, and the second… (more)

Subjects/Keywords: organic chemistry; reaction development; conjugate addition; BINOL; boronic acids; indoles; total synthesis; natural products; Chemistry

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APA (6th Edition):

Lundy, B. J. (2013). I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/950

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):

Lundy, Brian J. “I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY.” 2013. Thesis, University of Houston. Accessed July 18, 2019. http://hdl.handle.net/10657/950.

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

MLA Handbook (7th Edition):

Lundy, Brian J. “I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY.” 2013. Web. 18 Jul 2019.

Vancouver:

Lundy BJ. I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY. [Internet] [Thesis]. University of Houston; 2013. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/10657/950.

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

Council of Science Editors:

Lundy BJ. I) ENANTIOSELECTIVE CONJUGATE ADDITION OF ALKENYLBORONIC ACIDS TO INDOLE-APPENDED ENONES II) SYNTHETIC DEVELOPMENTS TOWARD THE APLYKURODIN FAMILY. [Thesis]. University of Houston; 2013. Available from: http://hdl.handle.net/10657/950

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


University of South Carolina

16. SUN, JING. Synthetic Lectins For Glycoprotein Recognition: towards the Identification and Classification of Cancer Associated Cell Lines.

Degree: PhD, Chemistry and Biochemistry, 2011, University of South Carolina

  Aberrant glycosylation occurs during the onset of the cancer and glycosylation patterns can provide information about different cancer types and metastatic potential. The work… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; aberrant glycosylation; boronic acids; cancer; sensor array; synthetic lectins

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APA (6th Edition):

SUN, J. (2011). Synthetic Lectins For Glycoprotein Recognition: towards the Identification and Classification of Cancer Associated Cell Lines. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/727

Chicago Manual of Style (16th Edition):

SUN, JING. “Synthetic Lectins For Glycoprotein Recognition: towards the Identification and Classification of Cancer Associated Cell Lines.” 2011. Doctoral Dissertation, University of South Carolina. Accessed July 18, 2019. https://scholarcommons.sc.edu/etd/727.

MLA Handbook (7th Edition):

SUN, JING. “Synthetic Lectins For Glycoprotein Recognition: towards the Identification and Classification of Cancer Associated Cell Lines.” 2011. Web. 18 Jul 2019.

Vancouver:

SUN J. Synthetic Lectins For Glycoprotein Recognition: towards the Identification and Classification of Cancer Associated Cell Lines. [Internet] [Doctoral dissertation]. University of South Carolina; 2011. [cited 2019 Jul 18]. Available from: https://scholarcommons.sc.edu/etd/727.

Council of Science Editors:

SUN J. Synthetic Lectins For Glycoprotein Recognition: towards the Identification and Classification of Cancer Associated Cell Lines. [Doctoral Dissertation]. University of South Carolina; 2011. Available from: https://scholarcommons.sc.edu/etd/727


University of South Carolina

17. Bicker, Kevin Lee. Bead Based Peptidyl Libraries for the Selective Recognition of Glycoproteins, Differentiation of Carcinogenic Cell Types, and Determination of Enzyme Substrate Specificity.

Degree: PhD, Chemistry and Biochemistry, 2010, University of South Carolina

  The aberrant glycosylation of integral cell membrane and secreted glycoproteins is a hallmark of carcinogenesis and presents a unique opportunity to detect cancer at… (more)

Subjects/Keywords: Chemistry; Physical Sciences and Mathematics; Aberrent Glycosylation; Arrays; Boronic Acids; Cancer; Sensors

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APA (6th Edition):

Bicker, K. L. (2010). Bead Based Peptidyl Libraries for the Selective Recognition of Glycoproteins, Differentiation of Carcinogenic Cell Types, and Determination of Enzyme Substrate Specificity. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/658

Chicago Manual of Style (16th Edition):

Bicker, Kevin Lee. “Bead Based Peptidyl Libraries for the Selective Recognition of Glycoproteins, Differentiation of Carcinogenic Cell Types, and Determination of Enzyme Substrate Specificity.” 2010. Doctoral Dissertation, University of South Carolina. Accessed July 18, 2019. https://scholarcommons.sc.edu/etd/658.

MLA Handbook (7th Edition):

Bicker, Kevin Lee. “Bead Based Peptidyl Libraries for the Selective Recognition of Glycoproteins, Differentiation of Carcinogenic Cell Types, and Determination of Enzyme Substrate Specificity.” 2010. Web. 18 Jul 2019.

Vancouver:

Bicker KL. Bead Based Peptidyl Libraries for the Selective Recognition of Glycoproteins, Differentiation of Carcinogenic Cell Types, and Determination of Enzyme Substrate Specificity. [Internet] [Doctoral dissertation]. University of South Carolina; 2010. [cited 2019 Jul 18]. Available from: https://scholarcommons.sc.edu/etd/658.

Council of Science Editors:

Bicker KL. Bead Based Peptidyl Libraries for the Selective Recognition of Glycoproteins, Differentiation of Carcinogenic Cell Types, and Determination of Enzyme Substrate Specificity. [Doctoral Dissertation]. University of South Carolina; 2010. Available from: https://scholarcommons.sc.edu/etd/658


Loughborough University

18. Sanchez-Ballester, Noelia M. Supramolecular studies with functionalised group 15 ligands.

Degree: 2010, Loughborough University

 This thesis has been divided into five sections. The first chapter introduces the main themes of this thesis, including the description of the concepts of… (more)

Subjects/Keywords: 547.05; Supramolecular chemistry; Hydrogen bonding; Single crystal X-ray diffraction; Pyridine-carboxylic acids; Solvates; Boronic acids; Co-crystal; Ditertiary phosphines; Pyrazine-carboxylic acids

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APA (6th Edition):

Sanchez-Ballester, N. M. (2010). Supramolecular studies with functionalised group 15 ligands. (Doctoral Dissertation). Loughborough University. Retrieved from https://dspace.lboro.ac.uk/2134/6062 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.519973

Chicago Manual of Style (16th Edition):

Sanchez-Ballester, Noelia M. “Supramolecular studies with functionalised group 15 ligands.” 2010. Doctoral Dissertation, Loughborough University. Accessed July 18, 2019. https://dspace.lboro.ac.uk/2134/6062 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.519973.

MLA Handbook (7th Edition):

Sanchez-Ballester, Noelia M. “Supramolecular studies with functionalised group 15 ligands.” 2010. Web. 18 Jul 2019.

Vancouver:

Sanchez-Ballester NM. Supramolecular studies with functionalised group 15 ligands. [Internet] [Doctoral dissertation]. Loughborough University; 2010. [cited 2019 Jul 18]. Available from: https://dspace.lboro.ac.uk/2134/6062 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.519973.

Council of Science Editors:

Sanchez-Ballester NM. Supramolecular studies with functionalised group 15 ligands. [Doctoral Dissertation]. Loughborough University; 2010. Available from: https://dspace.lboro.ac.uk/2134/6062 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.519973

19. Fournier, Rémi. Polymères associatifs par interaction covalente réversible diol-acide boronique : Associative polymers based on the diol-boronic acid reversible covalent interaction.

Degree: Docteur es, Physico-chimie de la Matière Molle, 2016, Université Pierre et Marie Curie – Paris VI

Ce travail de thèse porte sur la synthèse et l'étude physico-chimique de polymères associatifs hydrosolubles à associations complémentaires. Utilisant la chimie covalente réversible, ce système… (more)

Subjects/Keywords: Polymères associatifs; Rhéologie; Acides boroniques; Physico-Chimie; Rhéo-Microscopie; Gels; Associative polymers; Boronic acids; Rheology; 541.3

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APA (6th Edition):

Fournier, R. (2016). Polymères associatifs par interaction covalente réversible diol-acide boronique : Associative polymers based on the diol-boronic acid reversible covalent interaction. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066401

Chicago Manual of Style (16th Edition):

Fournier, Rémi. “Polymères associatifs par interaction covalente réversible diol-acide boronique : Associative polymers based on the diol-boronic acid reversible covalent interaction.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed July 18, 2019. http://www.theses.fr/2016PA066401.

MLA Handbook (7th Edition):

Fournier, Rémi. “Polymères associatifs par interaction covalente réversible diol-acide boronique : Associative polymers based on the diol-boronic acid reversible covalent interaction.” 2016. Web. 18 Jul 2019.

Vancouver:

Fournier R. Polymères associatifs par interaction covalente réversible diol-acide boronique : Associative polymers based on the diol-boronic acid reversible covalent interaction. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2019 Jul 18]. Available from: http://www.theses.fr/2016PA066401.

Council of Science Editors:

Fournier R. Polymères associatifs par interaction covalente réversible diol-acide boronique : Associative polymers based on the diol-boronic acid reversible covalent interaction. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066401


Université Montpellier II

20. Barbeyron, Renaud. Auto-assemblage d'acides borononucléiques : de la ligation à la polymérisation : Self-assembly of borononucleic acids : from ligation to polymerization.

Degree: Docteur es, Ingénierie moléculaire, 2014, Université Montpellier II

Mimer les processus biologiques par des méthodes s'affranchissant de la nécessité d'activation enzymatique est un défi pour la communauté des chimistes. Parmi ces processus nous… (more)

Subjects/Keywords: Auto-Assemblage; Acides nucléiques; Acides boroniques; Liaison internucléosidique réversible; Auto-Polymérisation; Self-Assembly; Nucleic acids; Boronic acids; Internucleosidic reversible linkage; Auto-Polymerization

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APA (6th Edition):

Barbeyron, R. (2014). Auto-assemblage d'acides borononucléiques : de la ligation à la polymérisation : Self-assembly of borononucleic acids : from ligation to polymerization. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2014MON20198

Chicago Manual of Style (16th Edition):

Barbeyron, Renaud. “Auto-assemblage d'acides borononucléiques : de la ligation à la polymérisation : Self-assembly of borononucleic acids : from ligation to polymerization.” 2014. Doctoral Dissertation, Université Montpellier II. Accessed July 18, 2019. http://www.theses.fr/2014MON20198.

MLA Handbook (7th Edition):

Barbeyron, Renaud. “Auto-assemblage d'acides borononucléiques : de la ligation à la polymérisation : Self-assembly of borononucleic acids : from ligation to polymerization.” 2014. Web. 18 Jul 2019.

Vancouver:

Barbeyron R. Auto-assemblage d'acides borononucléiques : de la ligation à la polymérisation : Self-assembly of borononucleic acids : from ligation to polymerization. [Internet] [Doctoral dissertation]. Université Montpellier II; 2014. [cited 2019 Jul 18]. Available from: http://www.theses.fr/2014MON20198.

Council of Science Editors:

Barbeyron R. Auto-assemblage d'acides borononucléiques : de la ligation à la polymérisation : Self-assembly of borononucleic acids : from ligation to polymerization. [Doctoral Dissertation]. Université Montpellier II; 2014. Available from: http://www.theses.fr/2014MON20198


Virginia Tech

21. Zhang, Wenyu. Targeting HIV-1 RNAs with Medium Sized Branched Peptides Featuring Boron and Acridine-Branched Peptide Library Design, Synthesis, High-Throughput Screening and Validation.

Degree: PhD, Chemistry, 2014, Virginia Tech

 RNAs have gained significant attention in recent years because they can fold into well-defined secondary or tertiary structures. These three dimensional architectures provide interfaces for… (more)

Subjects/Keywords: HIV-1; TAR RNA; RRE RNA; Branched Peptide Library; High-throughput Screening; Branched Peptide Boronic Acids; Acridine Branched Peptides; Unnatural Amino Acids

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APA (6th Edition):

Zhang, W. (2014). Targeting HIV-1 RNAs with Medium Sized Branched Peptides Featuring Boron and Acridine-Branched Peptide Library Design, Synthesis, High-Throughput Screening and Validation. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/56731

Chicago Manual of Style (16th Edition):

Zhang, Wenyu. “Targeting HIV-1 RNAs with Medium Sized Branched Peptides Featuring Boron and Acridine-Branched Peptide Library Design, Synthesis, High-Throughput Screening and Validation.” 2014. Doctoral Dissertation, Virginia Tech. Accessed July 18, 2019. http://hdl.handle.net/10919/56731.

MLA Handbook (7th Edition):

Zhang, Wenyu. “Targeting HIV-1 RNAs with Medium Sized Branched Peptides Featuring Boron and Acridine-Branched Peptide Library Design, Synthesis, High-Throughput Screening and Validation.” 2014. Web. 18 Jul 2019.

Vancouver:

Zhang W. Targeting HIV-1 RNAs with Medium Sized Branched Peptides Featuring Boron and Acridine-Branched Peptide Library Design, Synthesis, High-Throughput Screening and Validation. [Internet] [Doctoral dissertation]. Virginia Tech; 2014. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/10919/56731.

Council of Science Editors:

Zhang W. Targeting HIV-1 RNAs with Medium Sized Branched Peptides Featuring Boron and Acridine-Branched Peptide Library Design, Synthesis, High-Throughput Screening and Validation. [Doctoral Dissertation]. Virginia Tech; 2014. Available from: http://hdl.handle.net/10919/56731


EPFL

22. Christinat, Nicolas. Self-assembly of boron-based supramolecular structures.

Degree: 2008, EPFL

 This work describes the synthesis and characterization of boronic acid-based supramolecular structures. Macrocycles, dendritic structures, polymers, rotaxanes, and cages were assembled using four types of… (more)

Subjects/Keywords: Boronic acids; Self-assembly; Macrocycles; Imine; Multicomponent reactions; Polymers; Rotaxanes; Cages; Acides boroniques; Auto-assemblage; Macrocycles; Imines; Réactions à composants multiples; Polymères; Rotaxanes; Cages

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APA (6th Edition):

Christinat, N. (2008). Self-assembly of boron-based supramolecular structures. (Thesis). EPFL. Retrieved from http://infoscience.epfl.ch/record/125888

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):

Christinat, Nicolas. “Self-assembly of boron-based supramolecular structures.” 2008. Thesis, EPFL. Accessed July 18, 2019. http://infoscience.epfl.ch/record/125888.

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

MLA Handbook (7th Edition):

Christinat, Nicolas. “Self-assembly of boron-based supramolecular structures.” 2008. Web. 18 Jul 2019.

Vancouver:

Christinat N. Self-assembly of boron-based supramolecular structures. [Internet] [Thesis]. EPFL; 2008. [cited 2019 Jul 18]. Available from: http://infoscience.epfl.ch/record/125888.

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

Council of Science Editors:

Christinat N. Self-assembly of boron-based supramolecular structures. [Thesis]. EPFL; 2008. Available from: http://infoscience.epfl.ch/record/125888

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

23. Patil, Aditi S. Synthesis of alpha-Oxygenated Carbonyl Compounds via Dioxygenation, Development of Flourescent Probes.

Degree: 2014, University of Illinois – Chicago

 An alternative route to α-oxygenated carbonyl compounds through the dioxygenation of vinyl boronic acids has been developed. This new transformation avoids the use of unstable… (more)

Subjects/Keywords: Dioxygenation; Boronic Acids; Alpha-oxygenation; Diastereoselective alpha-oxygenation; [3,3]-rearrangement

…245 ix LIST OF SCHEMES SCHEMES PAGE Scheme 1.1 Aryl Boronic Acids in the Synthesis of… …Boronic Acids ...............................................3 Scheme 1.3 Petasis Reaction… …with Alkenyl Boronic Acids ...............................................4 Scheme 1.4… …11 Scheme 1.14 Using Alkenyl Boronic Acids… …13 Scheme 1.17 Dioxygenation of Alkenyl Boronic Acids… 

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APA (6th Edition):

Patil, A. S. (2014). Synthesis of alpha-Oxygenated Carbonyl Compounds via Dioxygenation, Development of Flourescent Probes. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/11234

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):

Patil, Aditi S. “Synthesis of alpha-Oxygenated Carbonyl Compounds via Dioxygenation, Development of Flourescent Probes.” 2014. Thesis, University of Illinois – Chicago. Accessed July 18, 2019. http://hdl.handle.net/10027/11234.

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

MLA Handbook (7th Edition):

Patil, Aditi S. “Synthesis of alpha-Oxygenated Carbonyl Compounds via Dioxygenation, Development of Flourescent Probes.” 2014. Web. 18 Jul 2019.

Vancouver:

Patil AS. Synthesis of alpha-Oxygenated Carbonyl Compounds via Dioxygenation, Development of Flourescent Probes. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2019 Jul 18]. Available from: http://hdl.handle.net/10027/11234.

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

Council of Science Editors:

Patil AS. Synthesis of alpha-Oxygenated Carbonyl Compounds via Dioxygenation, Development of Flourescent Probes. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/11234

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

24. Brown, James Robert David. Boronate-Diol Interactions in Membranes: A Biomimetic Tool for Polysaccharide Recognition.

Degree: 2013, University of Manchester

 Molecular recognition at biomembranes is one of the more poorly understood aspects of fundamental research in physical organic chemistry. Our aim was to improve our… (more)

Subjects/Keywords: Boronic acids; Saccharides; Molecular Recognition; Biomembranes; Ionophore; Ion Transport

…dramatic increase in fluorescence intensity upon heparin association.95 1.3 Boronic acids as… …recognition.99 Covalent interactions, such as those between boronic acids and diols have been… …Complexation of boronic acids with saccharides The interaction between a boronic acid and a diol is… …of the acidic proton.96 The ability of boronic acids to bind to diols was first observed in… …aromatic boronic acids and polyols.103 It was observed that addition of phenylboronic acid to a… 

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APA (6th Edition):

Brown, J. R. D. (2013). Boronate-Diol Interactions in Membranes: A Biomimetic Tool for Polysaccharide Recognition. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189076

Chicago Manual of Style (16th Edition):

Brown, James Robert David. “Boronate-Diol Interactions in Membranes: A Biomimetic Tool for Polysaccharide Recognition.” 2013. Doctoral Dissertation, University of Manchester. Accessed July 18, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189076.

MLA Handbook (7th Edition):

Brown, James Robert David. “Boronate-Diol Interactions in Membranes: A Biomimetic Tool for Polysaccharide Recognition.” 2013. Web. 18 Jul 2019.

Vancouver:

Brown JRD. Boronate-Diol Interactions in Membranes: A Biomimetic Tool for Polysaccharide Recognition. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Jul 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189076.

Council of Science Editors:

Brown JRD. Boronate-Diol Interactions in Membranes: A Biomimetic Tool for Polysaccharide Recognition. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:189076

25. Cazorla, Clément. Étude de la réactivité polyvalente des composés borés : de la fluoration électrophile à la synthèse d’amides par substitution nucléophile oxydante ; O-alkylation de dérivés phénoliques par substitution nucléophile : vers la mise au point d’un système éco-compatible : Versatile alkyl boronic reactivity : electrophilic fluorination and oxidative nucleophilic substitution for amide synthesis; O-Alkylation of phenols derivatives via a nucleophilic substitution.

Degree: Docteur es, Chimie, 2011, Université Claude Bernard – Lyon I

Ce travail a tout d’abord porté sur la réactivité des dérivés borés puis sur la réaction de O-alkylation des alcools aromatiques. L’utilisation des composés borés… (more)

Subjects/Keywords: Fluoration électrophile; Amidation; Acides boroniques; Sels de trifluoroborates; Substitution nucléophile oxydante; O-alkylation; Nafion® NR50; Electrophilic fluorination; Amidation; Boronic acids; Trifluoroborate salts; Oxidative nucleophilic substitution; O-alkylation; Nafion® NR50; 547

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APA (6th Edition):

Cazorla, C. (2011). Étude de la réactivité polyvalente des composés borés : de la fluoration électrophile à la synthèse d’amides par substitution nucléophile oxydante ; O-alkylation de dérivés phénoliques par substitution nucléophile : vers la mise au point d’un système éco-compatible : Versatile alkyl boronic reactivity : electrophilic fluorination and oxidative nucleophilic substitution for amide synthesis; O-Alkylation of phenols derivatives via a nucleophilic substitution. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2011LYO10144

Chicago Manual of Style (16th Edition):

Cazorla, Clément. “Étude de la réactivité polyvalente des composés borés : de la fluoration électrophile à la synthèse d’amides par substitution nucléophile oxydante ; O-alkylation de dérivés phénoliques par substitution nucléophile : vers la mise au point d’un système éco-compatible : Versatile alkyl boronic reactivity : electrophilic fluorination and oxidative nucleophilic substitution for amide synthesis; O-Alkylation of phenols derivatives via a nucleophilic substitution.” 2011. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed July 18, 2019. http://www.theses.fr/2011LYO10144.

MLA Handbook (7th Edition):

Cazorla, Clément. “Étude de la réactivité polyvalente des composés borés : de la fluoration électrophile à la synthèse d’amides par substitution nucléophile oxydante ; O-alkylation de dérivés phénoliques par substitution nucléophile : vers la mise au point d’un système éco-compatible : Versatile alkyl boronic reactivity : electrophilic fluorination and oxidative nucleophilic substitution for amide synthesis; O-Alkylation of phenols derivatives via a nucleophilic substitution.” 2011. Web. 18 Jul 2019.

Vancouver:

Cazorla C. Étude de la réactivité polyvalente des composés borés : de la fluoration électrophile à la synthèse d’amides par substitution nucléophile oxydante ; O-alkylation de dérivés phénoliques par substitution nucléophile : vers la mise au point d’un système éco-compatible : Versatile alkyl boronic reactivity : electrophilic fluorination and oxidative nucleophilic substitution for amide synthesis; O-Alkylation of phenols derivatives via a nucleophilic substitution. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2011. [cited 2019 Jul 18]. Available from: http://www.theses.fr/2011LYO10144.

Council of Science Editors:

Cazorla C. Étude de la réactivité polyvalente des composés borés : de la fluoration électrophile à la synthèse d’amides par substitution nucléophile oxydante ; O-alkylation de dérivés phénoliques par substitution nucléophile : vers la mise au point d’un système éco-compatible : Versatile alkyl boronic reactivity : electrophilic fluorination and oxidative nucleophilic substitution for amide synthesis; O-Alkylation of phenols derivatives via a nucleophilic substitution. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2011. Available from: http://www.theses.fr/2011LYO10144


Université Montpellier II

26. Martin, Anthony. Auto-assemblage dynamique et programmable d'acides borononucléiques - Développement de nouvelles méthodologies de synthèse utilisant le réactif de Bestmann-Ohira : Dynamic and programmable borononucleic acids self-assembly - Development of new synthetic methodologies involving the Bestmann-Ohira reagent.

Degree: Docteur es, Ingénérie Moléculaire, 2011, Université Montpellier II

La chimie des acides boroniques englobe de multiples domaines comme les sciences analytiques, la synthèse organique et inorganique, la chimie médicinale et thérapeutique. L'aptitude des… (more)

Subjects/Keywords: Acides boroniques; Acides nucléiques; Auto-assemblage; Liaisons covalentes réversibles; Lien internucléosidique; Réactif de Bestmann-Ohira; Boronic acids; Nucleic acids; Self-assembly; Reversible covalent bonds; DNA/RNA-Templated autoligation; Bestmann-Ohira reagent

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

APA (6th Edition):

Martin, A. (2011). Auto-assemblage dynamique et programmable d'acides borononucléiques - Développement de nouvelles méthodologies de synthèse utilisant le réactif de Bestmann-Ohira : Dynamic and programmable borononucleic acids self-assembly - Development of new synthetic methodologies involving the Bestmann-Ohira reagent. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2011MON20146

Chicago Manual of Style (16th Edition):

Martin, Anthony. “Auto-assemblage dynamique et programmable d'acides borononucléiques - Développement de nouvelles méthodologies de synthèse utilisant le réactif de Bestmann-Ohira : Dynamic and programmable borononucleic acids self-assembly - Development of new synthetic methodologies involving the Bestmann-Ohira reagent.” 2011. Doctoral Dissertation, Université Montpellier II. Accessed July 18, 2019. http://www.theses.fr/2011MON20146.

MLA Handbook (7th Edition):

Martin, Anthony. “Auto-assemblage dynamique et programmable d'acides borononucléiques - Développement de nouvelles méthodologies de synthèse utilisant le réactif de Bestmann-Ohira : Dynamic and programmable borononucleic acids self-assembly - Development of new synthetic methodologies involving the Bestmann-Ohira reagent.” 2011. Web. 18 Jul 2019.

Vancouver:

Martin A. Auto-assemblage dynamique et programmable d'acides borononucléiques - Développement de nouvelles méthodologies de synthèse utilisant le réactif de Bestmann-Ohira : Dynamic and programmable borononucleic acids self-assembly - Development of new synthetic methodologies involving the Bestmann-Ohira reagent. [Internet] [Doctoral dissertation]. Université Montpellier II; 2011. [cited 2019 Jul 18]. Available from: http://www.theses.fr/2011MON20146.

Council of Science Editors:

Martin A. Auto-assemblage dynamique et programmable d'acides borononucléiques - Développement de nouvelles méthodologies de synthèse utilisant le réactif de Bestmann-Ohira : Dynamic and programmable borononucleic acids self-assembly - Development of new synthetic methodologies involving the Bestmann-Ohira reagent. [Doctoral Dissertation]. Université Montpellier II; 2011. Available from: http://www.theses.fr/2011MON20146

27. Murphy, Christopher Lee William. Synthesis of Boronic Acids and Esters from Pinacolborane and Aminoborane Under Ambient Magnesium-, Iodine-, and Zinc-Mediated Conditions.

Degree: Chemistry, 2016, University of California – Santa Cruz

 Grignard reagents react with one equivalent of 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (pinacolborane, HBpin) at ambient temperatures in tetrahydrofuran (THF) to afford the corresponding pinacol boronate esters. Initially formed… (more)

Subjects/Keywords: Organic chemistry; Aminoborane; Boronate Esters; Boronic Acids; Grignard; Organozinc halide; Pinacolborane

…Figure 1.11. Proposed mechanism for Chan-Lam coupling of boronic acids with anilines or phenols… …Cl, Br, I 159 ix LIST OF SCHEMES Scheme 1.1. Ionization of boronic acids in water 5… …boronic acids via transmetalation of arylsilanes 16 Scheme 1.8. General procedure for the… …oligomers 35 Scheme 1.19. General conditions for the coupling of boronic acids with N-H, O-H, or… …cross-coupling with boronic acids and esters 41 Scheme 1.23. Equilibria of anthrylboronic… 

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APA (6th Edition):

Murphy, C. L. W. (2016). Synthesis of Boronic Acids and Esters from Pinacolborane and Aminoborane Under Ambient Magnesium-, Iodine-, and Zinc-Mediated Conditions. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/8dw380vb

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):

Murphy, Christopher Lee William. “Synthesis of Boronic Acids and Esters from Pinacolborane and Aminoborane Under Ambient Magnesium-, Iodine-, and Zinc-Mediated Conditions.” 2016. Thesis, University of California – Santa Cruz. Accessed July 18, 2019. http://www.escholarship.org/uc/item/8dw380vb.

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

MLA Handbook (7th Edition):

Murphy, Christopher Lee William. “Synthesis of Boronic Acids and Esters from Pinacolborane and Aminoborane Under Ambient Magnesium-, Iodine-, and Zinc-Mediated Conditions.” 2016. Web. 18 Jul 2019.

Vancouver:

Murphy CLW. Synthesis of Boronic Acids and Esters from Pinacolborane and Aminoborane Under Ambient Magnesium-, Iodine-, and Zinc-Mediated Conditions. [Internet] [Thesis]. University of California – Santa Cruz; 2016. [cited 2019 Jul 18]. Available from: http://www.escholarship.org/uc/item/8dw380vb.

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

Council of Science Editors:

Murphy CLW. Synthesis of Boronic Acids and Esters from Pinacolborane and Aminoborane Under Ambient Magnesium-, Iodine-, and Zinc-Mediated Conditions. [Thesis]. University of California – Santa Cruz; 2016. Available from: http://www.escholarship.org/uc/item/8dw380vb

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

28. Bailey, Christopher. Reactions of Diisopropylaminoborane and Metal Dialkylaminoborohydrides.

Degree: Chemistry, 2015, University of California – Santa Cruz

 Diisopropylaminoborane (H2B-N(iPr)2) is prepared as a monomer from the reaction of lithium diisopropylaminoborohydride with trimethylsilyl chloride at ambient conditions. Monomeric aminoboranes, such as H2B-N(iPr)2, can… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Aldehydes; Boronic Acids; Dialkylaminoborohydrides; Diisopropylaminoborane; Grignard Reagents; Reduction

…in the Synthesis of (+)Erythrococcamide B with Boronic Acids 43 Scheme 1.14… …and p-Iodoanisol 86 viii Scheme 3.1. Palladium-Catalyzed Synthesis of Boronic Acids from… …H2B-N(iPr)2 117 Scheme 3.4. Synthesis of Boronic Acids from H2B-N(iPr… …x28;iPr)2, Aryl Iodides, and Bromides 86 Table 3.1. Synthesis of boronic Acids from… …Commercial Grignard Reagents 120 Table 3.2. Synthesis of Boronic Acids Under Modified Barbier… 

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

APA (6th Edition):

Bailey, C. (2015). Reactions of Diisopropylaminoborane and Metal Dialkylaminoborohydrides. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/05x542f1

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):

Bailey, Christopher. “Reactions of Diisopropylaminoborane and Metal Dialkylaminoborohydrides.” 2015. Thesis, University of California – Santa Cruz. Accessed July 18, 2019. http://www.escholarship.org/uc/item/05x542f1.

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

MLA Handbook (7th Edition):

Bailey, Christopher. “Reactions of Diisopropylaminoborane and Metal Dialkylaminoborohydrides.” 2015. Web. 18 Jul 2019.

Vancouver:

Bailey C. Reactions of Diisopropylaminoborane and Metal Dialkylaminoborohydrides. [Internet] [Thesis]. University of California – Santa Cruz; 2015. [cited 2019 Jul 18]. Available from: http://www.escholarship.org/uc/item/05x542f1.

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

Council of Science Editors:

Bailey C. Reactions of Diisopropylaminoborane and Metal Dialkylaminoborohydrides. [Thesis]. University of California – Santa Cruz; 2015. Available from: http://www.escholarship.org/uc/item/05x542f1

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

29. Durganala, Sravanthi. Synthesis Of Non-Halogenated Flame Retardants For Polyurethane Foams.

Degree: MS(M.S.), Chemical Engineering, 2011, University of Dayton

  Polyurethanes are known to be the largest fuel loads which can easily ignite and once it ignites, lead to flashover, burning at fast rates.… (more)

Subjects/Keywords: Chemical Engineering; Chemistry; Organic Chemistry; flame retardants; polyurethane; non-halogenated; phosphorous; boronic acids

…thesis are centered on this approach. Flame retardants like boronic acids, cyclic phosphates… …x5B;21,9] 12 Among the boron based flame retardants boronic acids are of particular… …interest because during heating these boronic acids form boroxine network [Fig. 3]… …Preparation of boronic ester ...15 3. Preparation of boronoterephthalic acid… …water, to atmospheric conditions, to oils, greases, organic solvents, diluted acids and… 

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APA (6th Edition):

Durganala, S. (2011). Synthesis Of Non-Halogenated Flame Retardants For Polyurethane Foams. (Masters Thesis). University of Dayton. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=dayton1312338050

Chicago Manual of Style (16th Edition):

Durganala, Sravanthi. “Synthesis Of Non-Halogenated Flame Retardants For Polyurethane Foams.” 2011. Masters Thesis, University of Dayton. Accessed July 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1312338050.

MLA Handbook (7th Edition):

Durganala, Sravanthi. “Synthesis Of Non-Halogenated Flame Retardants For Polyurethane Foams.” 2011. Web. 18 Jul 2019.

Vancouver:

Durganala S. Synthesis Of Non-Halogenated Flame Retardants For Polyurethane Foams. [Internet] [Masters thesis]. University of Dayton; 2011. [cited 2019 Jul 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=dayton1312338050.

Council of Science Editors:

Durganala S. Synthesis Of Non-Halogenated Flame Retardants For Polyurethane Foams. [Masters Thesis]. University of Dayton; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=dayton1312338050

30. Bos, Maxence. Synthèse de [gamma]-lactones polyfonctionnelles chirales par catalyse énantiosélective : Catalytic enantioselective syntheses of polyfunctional chiral [gamma]-lactones.

Degree: Docteur es, Sciences - STS, 2015, Reims

La mise au point de méthodologies de synthèse permettant d’obtenir des substances énantiopures présentant une diversité structurale importante est une préoccupation majeure de la chimie… (more)

Subjects/Keywords: [GAMMA]-Lactone; 5-Hydroxyfuran-2(5H)-One; Catalyse Énantiosélective; Acides Boroniques; Réaction de Passerini; Alkylation Allylique Asymétrique; [GAMMA]-Lactone; 5-Hydroxyfuran-2(5H)-One; Enantioselective Catalysis; Boronic Acids; Passerini Reaction; Asymmetric Allylic Reaction

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

APA (6th Edition):

Bos, M. (2015). Synthèse de [gamma]-lactones polyfonctionnelles chirales par catalyse énantiosélective : Catalytic enantioselective syntheses of polyfunctional chiral [gamma]-lactones. (Doctoral Dissertation). Reims. Retrieved from http://www.theses.fr/2015REIMS017

Chicago Manual of Style (16th Edition):

Bos, Maxence. “Synthèse de [gamma]-lactones polyfonctionnelles chirales par catalyse énantiosélective : Catalytic enantioselective syntheses of polyfunctional chiral [gamma]-lactones.” 2015. Doctoral Dissertation, Reims. Accessed July 18, 2019. http://www.theses.fr/2015REIMS017.

MLA Handbook (7th Edition):

Bos, Maxence. “Synthèse de [gamma]-lactones polyfonctionnelles chirales par catalyse énantiosélective : Catalytic enantioselective syntheses of polyfunctional chiral [gamma]-lactones.” 2015. Web. 18 Jul 2019.

Vancouver:

Bos M. Synthèse de [gamma]-lactones polyfonctionnelles chirales par catalyse énantiosélective : Catalytic enantioselective syntheses of polyfunctional chiral [gamma]-lactones. [Internet] [Doctoral dissertation]. Reims; 2015. [cited 2019 Jul 18]. Available from: http://www.theses.fr/2015REIMS017.

Council of Science Editors:

Bos M. Synthèse de [gamma]-lactones polyfonctionnelles chirales par catalyse énantiosélective : Catalytic enantioselective syntheses of polyfunctional chiral [gamma]-lactones. [Doctoral Dissertation]. Reims; 2015. Available from: http://www.theses.fr/2015REIMS017

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