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You searched for subject:(hydroacylation). Showing records 1 – 19 of 19 total matches.

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1. Dheur, Julien. Hydroacylation carbonylante d'alcynes : nouvelle voie d'accès à des cétones alpha, béta-insaturées : Carbonylative hydroacylation on alkynes : a new access to alpha, beta-unsatured ketones.

Degree: Docteur es, Chimie organique et macromoléculaire, 2008, Université Lille I – Sciences et Technologies

Du fait de leur difonctionnalités et, donc, de par leur réactivité particulière, les cétones alpha,beta-insaturées interviennent dans de nombreux schémas de synthèse de molécules complexes… (more)

Subjects/Keywords: Hydroacylation; Acides boroniques; RMN sous pression

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APA (6th Edition):

Dheur, J. (2008). Hydroacylation carbonylante d'alcynes : nouvelle voie d'accès à des cétones alpha, béta-insaturées : Carbonylative hydroacylation on alkynes : a new access to alpha, beta-unsatured ketones. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2008LIL10113

Chicago Manual of Style (16th Edition):

Dheur, Julien. “Hydroacylation carbonylante d'alcynes : nouvelle voie d'accès à des cétones alpha, béta-insaturées : Carbonylative hydroacylation on alkynes : a new access to alpha, beta-unsatured ketones.” 2008. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed December 09, 2019. http://www.theses.fr/2008LIL10113.

MLA Handbook (7th Edition):

Dheur, Julien. “Hydroacylation carbonylante d'alcynes : nouvelle voie d'accès à des cétones alpha, béta-insaturées : Carbonylative hydroacylation on alkynes : a new access to alpha, beta-unsatured ketones.” 2008. Web. 09 Dec 2019.

Vancouver:

Dheur J. Hydroacylation carbonylante d'alcynes : nouvelle voie d'accès à des cétones alpha, béta-insaturées : Carbonylative hydroacylation on alkynes : a new access to alpha, beta-unsatured ketones. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2008. [cited 2019 Dec 09]. Available from: http://www.theses.fr/2008LIL10113.

Council of Science Editors:

Dheur J. Hydroacylation carbonylante d'alcynes : nouvelle voie d'accès à des cétones alpha, béta-insaturées : Carbonylative hydroacylation on alkynes : a new access to alpha, beta-unsatured ketones. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2008. Available from: http://www.theses.fr/2008LIL10113


University of California – Irvine

2. Kim, Daniel Kwanwoo. Pushing the Boundaries of Hydroacylation: Development of Rhodium- and Cobalt-Catalyzed Reactions.

Degree: Chemistry, 2017, University of California – Irvine

 Cross-couplings that proceed via C–H bond activation streamline the synthesis of complex molecules. Rhodium complexes are promising catalysts for these reactions and they readily activate… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Cobalt; Hydroacylation; Rhodium

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APA (6th Edition):

Kim, D. K. (2017). Pushing the Boundaries of Hydroacylation: Development of Rhodium- and Cobalt-Catalyzed Reactions. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/3p68z1gh

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):

Kim, Daniel Kwanwoo. “Pushing the Boundaries of Hydroacylation: Development of Rhodium- and Cobalt-Catalyzed Reactions.” 2017. Thesis, University of California – Irvine. Accessed December 09, 2019. http://www.escholarship.org/uc/item/3p68z1gh.

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

MLA Handbook (7th Edition):

Kim, Daniel Kwanwoo. “Pushing the Boundaries of Hydroacylation: Development of Rhodium- and Cobalt-Catalyzed Reactions.” 2017. Web. 09 Dec 2019.

Vancouver:

Kim DK. Pushing the Boundaries of Hydroacylation: Development of Rhodium- and Cobalt-Catalyzed Reactions. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2019 Dec 09]. Available from: http://www.escholarship.org/uc/item/3p68z1gh.

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

Council of Science Editors:

Kim DK. Pushing the Boundaries of Hydroacylation: Development of Rhodium- and Cobalt-Catalyzed Reactions. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/3p68z1gh

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


Iowa State University

3. Walker Jr., James Alfonzo. Methods for alkene difunctionalizations: hydroacylation & carboacylation.

Degree: 2017, Iowa State University

 This thesis presents the development of new catalyst for the coupling of alkene hydroacylation and enantioselective α-arylation to form heterocyclic ketones containing α-chiral quarternary stereocenters,… (more)

Subjects/Keywords: carboacylation; hydroacylation; N-heterocyclic carbenes; Organic Chemistry

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APA (6th Edition):

Walker Jr., J. A. (2017). Methods for alkene difunctionalizations: hydroacylation & carboacylation. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/16752

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):

Walker Jr., James Alfonzo. “Methods for alkene difunctionalizations: hydroacylation & carboacylation.” 2017. Thesis, Iowa State University. Accessed December 09, 2019. https://lib.dr.iastate.edu/etd/16752.

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

MLA Handbook (7th Edition):

Walker Jr., James Alfonzo. “Methods for alkene difunctionalizations: hydroacylation & carboacylation.” 2017. Web. 09 Dec 2019.

Vancouver:

Walker Jr. JA. Methods for alkene difunctionalizations: hydroacylation & carboacylation. [Internet] [Thesis]. Iowa State University; 2017. [cited 2019 Dec 09]. Available from: https://lib.dr.iastate.edu/etd/16752.

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

Council of Science Editors:

Walker Jr. JA. Methods for alkene difunctionalizations: hydroacylation & carboacylation. [Thesis]. Iowa State University; 2017. Available from: https://lib.dr.iastate.edu/etd/16752

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


Iowa State University

4. Johnson, Kirsten Faye. Transition metal-catalyzed C-N and C-C bond formation: N-tert-prenylation and alkene hydroacylation.

Degree: 2016, Iowa State University

 This thesis presents the development of new catalysts for the palladium-catalyzed N-tert-prenylation of indoles, the rhodium-catalyzed endo- and enantioselective hydroacylation of ortho-allylbenzaldehydes, studies toward the… (more)

Subjects/Keywords: Hydroacylation; Palladium; Prenylation; Rhodium; Chemistry; Organic Chemistry

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APA (6th Edition):

Johnson, K. F. (2016). Transition metal-catalyzed C-N and C-C bond formation: N-tert-prenylation and alkene hydroacylation. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/15729

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):

Johnson, Kirsten Faye. “Transition metal-catalyzed C-N and C-C bond formation: N-tert-prenylation and alkene hydroacylation.” 2016. Thesis, Iowa State University. Accessed December 09, 2019. https://lib.dr.iastate.edu/etd/15729.

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

MLA Handbook (7th Edition):

Johnson, Kirsten Faye. “Transition metal-catalyzed C-N and C-C bond formation: N-tert-prenylation and alkene hydroacylation.” 2016. Web. 09 Dec 2019.

Vancouver:

Johnson KF. Transition metal-catalyzed C-N and C-C bond formation: N-tert-prenylation and alkene hydroacylation. [Internet] [Thesis]. Iowa State University; 2016. [cited 2019 Dec 09]. Available from: https://lib.dr.iastate.edu/etd/15729.

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

Council of Science Editors:

Johnson KF. Transition metal-catalyzed C-N and C-C bond formation: N-tert-prenylation and alkene hydroacylation. [Thesis]. Iowa State University; 2016. Available from: https://lib.dr.iastate.edu/etd/15729

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


University of Toronto

5. Le, Christine. Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products.

Degree: 2012, University of Toronto

Transition metal-catalyzed olefin hydroacylation represents an atom-economical approach for the synthesis of valuable ketone products. To date, the intermolecular variant of this reaction suffers from… (more)

Subjects/Keywords: Hydroacylation; Octaketide natural product; Rhodium-catalysis; 0490

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APA (6th Edition):

Le, C. (2012). Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33305

Chicago Manual of Style (16th Edition):

Le, Christine. “Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products.” 2012. Masters Thesis, University of Toronto. Accessed December 09, 2019. http://hdl.handle.net/1807/33305.

MLA Handbook (7th Edition):

Le, Christine. “Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products.” 2012. Web. 09 Dec 2019.

Vancouver:

Le C. Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1807/33305.

Council of Science Editors:

Le C. Rhodium-catalyzed Intermolecular Hydroacylation of Unactivated Alkenes and Application to the Total Synthesis of Octaketide Natural Products. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33305


University of California – Irvine

6. Burt, Craig McLaughry. C–H Activation for Use in Total Synthesis and Tandem Oxidation-Dehydroformylation.

Degree: Chemistry, 2015, University of California – Irvine

 Chapter 1 focuses on the use of C–H activation in total synthesis and the strategies that these methods enable. Following a review of recent total… (more)

Subjects/Keywords: Organic chemistry; C-H activation; Dehydroformylation; Hydroacylation; Total Synthesis

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APA (6th Edition):

Burt, C. M. (2015). C–H Activation for Use in Total Synthesis and Tandem Oxidation-Dehydroformylation. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/3wm8235q

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):

Burt, Craig McLaughry. “C–H Activation for Use in Total Synthesis and Tandem Oxidation-Dehydroformylation.” 2015. Thesis, University of California – Irvine. Accessed December 09, 2019. http://www.escholarship.org/uc/item/3wm8235q.

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

MLA Handbook (7th Edition):

Burt, Craig McLaughry. “C–H Activation for Use in Total Synthesis and Tandem Oxidation-Dehydroformylation.” 2015. Web. 09 Dec 2019.

Vancouver:

Burt CM. C–H Activation for Use in Total Synthesis and Tandem Oxidation-Dehydroformylation. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2019 Dec 09]. Available from: http://www.escholarship.org/uc/item/3wm8235q.

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

Council of Science Editors:

Burt CM. C–H Activation for Use in Total Synthesis and Tandem Oxidation-Dehydroformylation. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/3wm8235q

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


University of Victoria

7. Theron, Robin. Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy.

Degree: Department of Chemistry, 2015, University of Victoria

 Electrospray ionization mass spectrometry (ESI-MS) has been applied to the realtime study of homogeneous organometallic reactions. ESI-MS as a soft ionization technique is amenable to… (more)

Subjects/Keywords: Mass spectormetry; Infrared spectroscopy; Catalysis; Chemistry; operando spectroscopy; hydroacylation; hydrogenation; hydroboration

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APA (6th Edition):

Theron, R. (2015). Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy. (Masters Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/6322

Chicago Manual of Style (16th Edition):

Theron, Robin. “Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy.” 2015. Masters Thesis, University of Victoria. Accessed December 09, 2019. http://hdl.handle.net/1828/6322.

MLA Handbook (7th Edition):

Theron, Robin. “Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy.” 2015. Web. 09 Dec 2019.

Vancouver:

Theron R. Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy. [Internet] [Masters thesis]. University of Victoria; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1828/6322.

Council of Science Editors:

Theron R. Real-time Investigation of Catalytic Reaction Mechanisms by Mass Spectrometry and Infrared Spectroscopy. [Masters Thesis]. University of Victoria; 2015. Available from: http://hdl.handle.net/1828/6322


Iowa State University

8. Ghosh, Avipsa. Transition Metal-Catalyzed Alkene Hydroacylation as a Platform for Enantioselective Synthesis of Polycyclic Nitrogen Heterocycles.

Degree: 2016, Iowa State University

 The prevalence of nitrogen heterocycles in medicinally important compounds has, for years, inspired synthetic chemists for developing strategies to form new heterocyclic scaffolds and methods… (more)

Subjects/Keywords: arylation; enantioselective; hydroacylation; nitrogen heterocycles; organometallic; quaternary center; Chemistry; Organic Chemistry

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APA (6th Edition):

Ghosh, A. (2016). Transition Metal-Catalyzed Alkene Hydroacylation as a Platform for Enantioselective Synthesis of Polycyclic Nitrogen Heterocycles. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/15919

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):

Ghosh, Avipsa. “Transition Metal-Catalyzed Alkene Hydroacylation as a Platform for Enantioselective Synthesis of Polycyclic Nitrogen Heterocycles.” 2016. Thesis, Iowa State University. Accessed December 09, 2019. https://lib.dr.iastate.edu/etd/15919.

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

MLA Handbook (7th Edition):

Ghosh, Avipsa. “Transition Metal-Catalyzed Alkene Hydroacylation as a Platform for Enantioselective Synthesis of Polycyclic Nitrogen Heterocycles.” 2016. Web. 09 Dec 2019.

Vancouver:

Ghosh A. Transition Metal-Catalyzed Alkene Hydroacylation as a Platform for Enantioselective Synthesis of Polycyclic Nitrogen Heterocycles. [Internet] [Thesis]. Iowa State University; 2016. [cited 2019 Dec 09]. Available from: https://lib.dr.iastate.edu/etd/15919.

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

Council of Science Editors:

Ghosh A. Transition Metal-Catalyzed Alkene Hydroacylation as a Platform for Enantioselective Synthesis of Polycyclic Nitrogen Heterocycles. [Thesis]. Iowa State University; 2016. Available from: https://lib.dr.iastate.edu/etd/15919

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

9. Longobardi, Lauren Elizabeth. Rhodium-catalyzed Intermolecular Ketone Hydroacylation: Towards an Enantioselective and Diastereoselective Protocol.

Degree: 2012, University of Toronto

The addition of an aldehyde C−H bond across a ketone functionality, formally a hydroacylation, has emerged as an atom-economical approach to the synthesis of esters.… (more)

Subjects/Keywords: Catalysis; Hydroacylation; 0490

hydroacylation… …5 Scheme 1.4: First example of a transition metal-catalyzed ketone hydroacylation, using a… …hydroacylation… …intramolecular ketone hydroacylation… …hydroacylation… 

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APA (6th Edition):

Longobardi, L. E. (2012). Rhodium-catalyzed Intermolecular Ketone Hydroacylation: Towards an Enantioselective and Diastereoselective Protocol. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42398

Chicago Manual of Style (16th Edition):

Longobardi, Lauren Elizabeth. “Rhodium-catalyzed Intermolecular Ketone Hydroacylation: Towards an Enantioselective and Diastereoselective Protocol.” 2012. Masters Thesis, University of Toronto. Accessed December 09, 2019. http://hdl.handle.net/1807/42398.

MLA Handbook (7th Edition):

Longobardi, Lauren Elizabeth. “Rhodium-catalyzed Intermolecular Ketone Hydroacylation: Towards an Enantioselective and Diastereoselective Protocol.” 2012. Web. 09 Dec 2019.

Vancouver:

Longobardi LE. Rhodium-catalyzed Intermolecular Ketone Hydroacylation: Towards an Enantioselective and Diastereoselective Protocol. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1807/42398.

Council of Science Editors:

Longobardi LE. Rhodium-catalyzed Intermolecular Ketone Hydroacylation: Towards an Enantioselective and Diastereoselective Protocol. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/42398


University of Oxford

10. Pernik, Indrek. Exploring small bite-angle PNP and PCP ligands for the rhodium-catalysed intermolecular hydroacylation of b-s-substituted aldehydes with alkenes and alkynes.

Degree: PhD, 2014, University of Oxford

 This thesis discusses the intermolecular hydroacylation reaction using cationic rhodium bis- phosphine complexes as catalysts. A series of small bite-angle rhodium bis-phosphine complexes have been… (more)

Subjects/Keywords: 547; Organometallic Chemistry; Catalysis; rhodium; phosphine; small bite-angle; hydroacylation; homogeneous catalysis

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APA (6th Edition):

Pernik, I. (2014). Exploring small bite-angle PNP and PCP ligands for the rhodium-catalysed intermolecular hydroacylation of b-s-substituted aldehydes with alkenes and alkynes. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:aaf41dc2-1147-44f4-b609-5bf7ada1b060 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635294

Chicago Manual of Style (16th Edition):

Pernik, Indrek. “Exploring small bite-angle PNP and PCP ligands for the rhodium-catalysed intermolecular hydroacylation of b-s-substituted aldehydes with alkenes and alkynes.” 2014. Doctoral Dissertation, University of Oxford. Accessed December 09, 2019. http://ora.ox.ac.uk/objects/uuid:aaf41dc2-1147-44f4-b609-5bf7ada1b060 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635294.

MLA Handbook (7th Edition):

Pernik, Indrek. “Exploring small bite-angle PNP and PCP ligands for the rhodium-catalysed intermolecular hydroacylation of b-s-substituted aldehydes with alkenes and alkynes.” 2014. Web. 09 Dec 2019.

Vancouver:

Pernik I. Exploring small bite-angle PNP and PCP ligands for the rhodium-catalysed intermolecular hydroacylation of b-s-substituted aldehydes with alkenes and alkynes. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2019 Dec 09]. Available from: http://ora.ox.ac.uk/objects/uuid:aaf41dc2-1147-44f4-b609-5bf7ada1b060 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635294.

Council of Science Editors:

Pernik I. Exploring small bite-angle PNP and PCP ligands for the rhodium-catalysed intermolecular hydroacylation of b-s-substituted aldehydes with alkenes and alkynes. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:aaf41dc2-1147-44f4-b609-5bf7ada1b060 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.635294


University of Oxford

11. Pawley, Rebekah J. Controlling selectivity in the rhodium-catalysed intermolecular hydroacylation reaction.

Degree: PhD, 2012, University of Oxford

 This thesis explores the area of the intermolecular hydroacylation reaction, catalysed by rhodium diphosphine complexes. A range of latent low-coordinate rhodium diphosphine complexes have been… (more)

Subjects/Keywords: 541.395; Organometallic Chemistry; Inorganic chemistry; organometallic; inorganic; chemistry; catalysis; rhodium; phosphine; hydroacylation

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APA (6th Edition):

Pawley, R. J. (2012). Controlling selectivity in the rhodium-catalysed intermolecular hydroacylation reaction. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:bef3f72f-7f18-4c5e-a6d6-e4e83f097b4d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.572890

Chicago Manual of Style (16th Edition):

Pawley, Rebekah J. “Controlling selectivity in the rhodium-catalysed intermolecular hydroacylation reaction.” 2012. Doctoral Dissertation, University of Oxford. Accessed December 09, 2019. http://ora.ox.ac.uk/objects/uuid:bef3f72f-7f18-4c5e-a6d6-e4e83f097b4d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.572890.

MLA Handbook (7th Edition):

Pawley, Rebekah J. “Controlling selectivity in the rhodium-catalysed intermolecular hydroacylation reaction.” 2012. Web. 09 Dec 2019.

Vancouver:

Pawley RJ. Controlling selectivity in the rhodium-catalysed intermolecular hydroacylation reaction. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2019 Dec 09]. Available from: http://ora.ox.ac.uk/objects/uuid:bef3f72f-7f18-4c5e-a6d6-e4e83f097b4d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.572890.

Council of Science Editors:

Pawley RJ. Controlling selectivity in the rhodium-catalysed intermolecular hydroacylation reaction. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:bef3f72f-7f18-4c5e-a6d6-e4e83f097b4d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.572890


Boston College

12. Nam, Youn Hee. Development of Ru-Catalyzed Tandem Sequences Involving Ring-Closing Metathesis.

Degree: PhD, Chemistry, 2013, Boston College

 Tandem processes can have several advantages over multiple single step processes. Non-metathesis transformations of ruthenium alkylidenes were studied and applied to tandem processes. Ruthenium catalyzed… (more)

Subjects/Keywords: C-H Activation; Hydroacylation; Olefin Isomerization; Ring-Closing Metathesis; Ru-Catalyzed; Tandem Sequence

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APA (6th Edition):

Nam, Y. H. (2013). Development of Ru-Catalyzed Tandem Sequences Involving Ring-Closing Metathesis. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101868

Chicago Manual of Style (16th Edition):

Nam, Youn Hee. “Development of Ru-Catalyzed Tandem Sequences Involving Ring-Closing Metathesis.” 2013. Doctoral Dissertation, Boston College. Accessed December 09, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101868.

MLA Handbook (7th Edition):

Nam, Youn Hee. “Development of Ru-Catalyzed Tandem Sequences Involving Ring-Closing Metathesis.” 2013. Web. 09 Dec 2019.

Vancouver:

Nam YH. Development of Ru-Catalyzed Tandem Sequences Involving Ring-Closing Metathesis. [Internet] [Doctoral dissertation]. Boston College; 2013. [cited 2019 Dec 09]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101868.

Council of Science Editors:

Nam YH. Development of Ru-Catalyzed Tandem Sequences Involving Ring-Closing Metathesis. [Doctoral Dissertation]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101868


University of Oxford

13. Lenden, Philip. Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation.

Degree: PhD, 2011, University of Oxford

 This work describes the extension of rhodium-catalysed intermolecular hydroacylation to encompass some tandem catalytic processes, wherein a further catalytic process is enacted on the product… (more)

Subjects/Keywords: 547.215; Chemistry & allied sciences; Catalysis; Heterocyclic chemistry; Organic chemistry; Organic synthesis; Organometallic Chemistry; Synthetic organic chemistry; chemistry; catalysis; heterocycles; rhodium; hydroacylation

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APA (6th Edition):

Lenden, P. (2011). Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:e63f5fd7-f92f-47dd-b06f-face73729804 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555255

Chicago Manual of Style (16th Edition):

Lenden, Philip. “Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation.” 2011. Doctoral Dissertation, University of Oxford. Accessed December 09, 2019. http://ora.ox.ac.uk/objects/uuid:e63f5fd7-f92f-47dd-b06f-face73729804 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555255.

MLA Handbook (7th Edition):

Lenden, Philip. “Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation.” 2011. Web. 09 Dec 2019.

Vancouver:

Lenden P. Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Dec 09]. Available from: http://ora.ox.ac.uk/objects/uuid:e63f5fd7-f92f-47dd-b06f-face73729804 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555255.

Council of Science Editors:

Lenden P. Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:e63f5fd7-f92f-47dd-b06f-face73729804 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555255


University of Oxford

14. Poingdestre, Sarah-Jane. Exploring and exploiting selectivity in rhodium-catalysed hydroacylation reactions.

Degree: PhD, 2012, University of Oxford

 Chapter 1 is an overview of the key developments in rhodium-catalysed hydroacylation. The main focus of this chapter is the use of various chelation strategies… (more)

Subjects/Keywords: 546.634; Physical Sciences; Chemistry & allied sciences; Organic chemistry; Organic synthesis; Synthetic organic chemistry; rhodium; selectivity; regioselectivity; hydroacylation; catalysis

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APA (6th Edition):

Poingdestre, S. (2012). Exploring and exploiting selectivity in rhodium-catalysed hydroacylation reactions. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:f2993627-6550-42a5-b6e1-9d63f8268dbb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581148

Chicago Manual of Style (16th Edition):

Poingdestre, Sarah-Jane. “Exploring and exploiting selectivity in rhodium-catalysed hydroacylation reactions.” 2012. Doctoral Dissertation, University of Oxford. Accessed December 09, 2019. http://ora.ox.ac.uk/objects/uuid:f2993627-6550-42a5-b6e1-9d63f8268dbb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581148.

MLA Handbook (7th Edition):

Poingdestre, Sarah-Jane. “Exploring and exploiting selectivity in rhodium-catalysed hydroacylation reactions.” 2012. Web. 09 Dec 2019.

Vancouver:

Poingdestre S. Exploring and exploiting selectivity in rhodium-catalysed hydroacylation reactions. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2019 Dec 09]. Available from: http://ora.ox.ac.uk/objects/uuid:f2993627-6550-42a5-b6e1-9d63f8268dbb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581148.

Council of Science Editors:

Poingdestre S. Exploring and exploiting selectivity in rhodium-catalysed hydroacylation reactions. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:f2993627-6550-42a5-b6e1-9d63f8268dbb ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581148


University of Oxford

15. Ylioja, Paul M. Rhodium catalysed hydroacylation reactions in the synthesis of heterocycles.

Degree: PhD, 2011, University of Oxford

 Rhodium-catalysed hydroacylation provides a highly atom economic synthesis of ketone products from the combination of aldehydes and multiple bond systems by C-H bond activation. This… (more)

Subjects/Keywords: 547.59; Organic chemistry; Organic synthesis; Catalysis; Heterocyclic chemistry; Organometallic Chemistry; Synthetic organic chemistry; rhodium; pyrroles; hydroacylation; enones; propargylamines; propargyl

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

APA (6th Edition):

Ylioja, P. M. (2011). Rhodium catalysed hydroacylation reactions in the synthesis of heterocycles. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:0bd31ddc-c13e-4502-b359-64495a297489 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580873

Chicago Manual of Style (16th Edition):

Ylioja, Paul M. “Rhodium catalysed hydroacylation reactions in the synthesis of heterocycles.” 2011. Doctoral Dissertation, University of Oxford. Accessed December 09, 2019. http://ora.ox.ac.uk/objects/uuid:0bd31ddc-c13e-4502-b359-64495a297489 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580873.

MLA Handbook (7th Edition):

Ylioja, Paul M. “Rhodium catalysed hydroacylation reactions in the synthesis of heterocycles.” 2011. Web. 09 Dec 2019.

Vancouver:

Ylioja PM. Rhodium catalysed hydroacylation reactions in the synthesis of heterocycles. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Dec 09]. Available from: http://ora.ox.ac.uk/objects/uuid:0bd31ddc-c13e-4502-b359-64495a297489 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580873.

Council of Science Editors:

Ylioja PM. Rhodium catalysed hydroacylation reactions in the synthesis of heterocycles. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:0bd31ddc-c13e-4502-b359-64495a297489 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580873


University of Minnesota

16. Beletskiy, Evgeny V. From catalysis to anion recognition.

Degree: PhD, Chemistry, 2014, University of Minnesota

 Part 1. A novel approach to enantioselective hydroacylation. A known methodology for hydroacylation of monosubstituted alkenes utilizing 2-amino-3-picoline as a temporary directing group was studied… (more)

Subjects/Keywords: 1,3,5-triaryl benzene; Anion receptors and their applications; Enantioselective hydroacylation; Hydrogen bond catalysis; Phosphate binding and detection; Three-pronged oxyanion hole

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APA (6th Edition):

Beletskiy, E. V. (2014). From catalysis to anion recognition. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/162920

Chicago Manual of Style (16th Edition):

Beletskiy, Evgeny V. “From catalysis to anion recognition.” 2014. Doctoral Dissertation, University of Minnesota. Accessed December 09, 2019. http://hdl.handle.net/11299/162920.

MLA Handbook (7th Edition):

Beletskiy, Evgeny V. “From catalysis to anion recognition.” 2014. Web. 09 Dec 2019.

Vancouver:

Beletskiy EV. From catalysis to anion recognition. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/11299/162920.

Council of Science Editors:

Beletskiy EV. From catalysis to anion recognition. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/162920

17. 臼井, 明日香. ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発.

Degree: 博士(理学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第18808号

理博第4066号

Subjects/Keywords: hypervalent iodine(III) reagents; radical reactions; C-H activation; site-selective oxidation; photo-catalyzed reaction; hydroacylation

Page 1 Page 2 Page 3

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APA (6th Edition):

臼井, . (2015). ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/199117 ; http://dx.doi.org/10.14989/doctor.k18808

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):

臼井, 明日香. “ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発.” 2015. Thesis, Kyoto University / 京都大学. Accessed December 09, 2019. http://hdl.handle.net/2433/199117 ; http://dx.doi.org/10.14989/doctor.k18808.

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

MLA Handbook (7th Edition):

臼井, 明日香. “ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発.” 2015. Web. 09 Dec 2019.

Vancouver:

臼井 . ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2433/199117 ; http://dx.doi.org/10.14989/doctor.k18808.

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

Council of Science Editors:

臼井 . ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/199117 ; http://dx.doi.org/10.14989/doctor.k18808

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


Kyoto University

18. 臼井, 明日香. ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発 .

Degree: 2015, Kyoto University

Subjects/Keywords: hypervalent iodine(III) reagents; radical reactions; C-H activation; site-selective oxidation; photo-catalyzed reaction; hydroacylation

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

APA (6th Edition):

臼井, . (2015). ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発 . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/199117

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):

臼井, 明日香. “ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発 .” 2015. Thesis, Kyoto University. Accessed December 09, 2019. http://hdl.handle.net/2433/199117.

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

MLA Handbook (7th Edition):

臼井, 明日香. “ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発 .” 2015. Web. 09 Dec 2019.

Vancouver:

臼井 . ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発 . [Internet] [Thesis]. Kyoto University; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2433/199117.

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

Council of Science Editors:

臼井 . ラジカル超原子価ヨウ素(III)試薬を用いた直接的C-H活性化反応の開発 . [Thesis]. Kyoto University; 2015. Available from: http://hdl.handle.net/2433/199117

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


Universitat Rovira i Virgili

19. Marcé Villa, Patricia. Hydroacylation and C-N Coupling Reactions. Mechanistic Studies and Application in the Nucleoside Synthesis.

Degree: Departament de Química Analítica i Química Orgànica, 2008, Universitat Rovira i Virgili

 Durante la última década la terapia del SIDA ha experimentado una evolución notable. El conocimiento del modo de actuación y proliferación del virus ha permitido… (more)

Subjects/Keywords: Mechanistic Studies by DFT and NMR; Synthesis of Carbocyclic Nucleoside; C-N couplings; Hydroacylation intermolecular and Intermolecylar; 544; 546; 547

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APA (6th Edition):

Marcé Villa, P. (2008). Hydroacylation and C-N Coupling Reactions. Mechanistic Studies and Application in the Nucleoside Synthesis. (Thesis). Universitat Rovira i Virgili. Retrieved from http://hdl.handle.net/10803/9026

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):

Marcé Villa, Patricia. “Hydroacylation and C-N Coupling Reactions. Mechanistic Studies and Application in the Nucleoside Synthesis.” 2008. Thesis, Universitat Rovira i Virgili. Accessed December 09, 2019. http://hdl.handle.net/10803/9026.

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

MLA Handbook (7th Edition):

Marcé Villa, Patricia. “Hydroacylation and C-N Coupling Reactions. Mechanistic Studies and Application in the Nucleoside Synthesis.” 2008. Web. 09 Dec 2019.

Vancouver:

Marcé Villa P. Hydroacylation and C-N Coupling Reactions. Mechanistic Studies and Application in the Nucleoside Synthesis. [Internet] [Thesis]. Universitat Rovira i Virgili; 2008. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10803/9026.

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

Council of Science Editors:

Marcé Villa P. Hydroacylation and C-N Coupling Reactions. Mechanistic Studies and Application in the Nucleoside Synthesis. [Thesis]. Universitat Rovira i Virgili; 2008. Available from: http://hdl.handle.net/10803/9026

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

.