Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Rearrangement). Showing records 1 – 30 of 350 total matches.

[1] [2] [3] [4] [5] … [12]

Search Limiters

Last 2 Years | English Only

Department

Degrees

Levels

Languages

Country

▼ Search Limiters


Vilnius University

1. Čiuladaitė, Živilė. Chromosomų struktūros persitvarkymų įvairovė Lietuvoje ir genetinė jų reikšmė.

Degree: Master, 2011, Vilnius University

Chromosomų struktūros persitvarkymai gali lemti įvairius žmogaus sveikatos sutrikimus. Netgi chromosominės ligos, pvz., Dauno ar Ternerio sindromai, gali būti nulemtos ne chromosomų skaičiaus, bet chromosomų… (more)

Subjects/Keywords: Chromosome; Rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Čiuladaitė, Živilė. (2011). Chromosomų struktūros persitvarkymų įvairovė Lietuvoje ir genetinė jų reikšmė. (Masters Thesis). Vilnius University. Retrieved from http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2008~D_20110709_152250-31963 ;

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

Chicago Manual of Style (16th Edition):

Čiuladaitė, Živilė. “Chromosomų struktūros persitvarkymų įvairovė Lietuvoje ir genetinė jų reikšmė.” 2011. Masters Thesis, Vilnius University. Accessed October 23, 2019. http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2008~D_20110709_152250-31963 ;.

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

MLA Handbook (7th Edition):

Čiuladaitė, Živilė. “Chromosomų struktūros persitvarkymų įvairovė Lietuvoje ir genetinė jų reikšmė.” 2011. Web. 23 Oct 2019.

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

Vancouver:

Čiuladaitė, Živilė. Chromosomų struktūros persitvarkymų įvairovė Lietuvoje ir genetinė jų reikšmė. [Internet] [Masters thesis]. Vilnius University; 2011. [cited 2019 Oct 23]. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2008~D_20110709_152250-31963 ;.

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

Council of Science Editors:

Čiuladaitė, Živilė. Chromosomų struktūros persitvarkymų įvairovė Lietuvoje ir genetinė jų reikšmė. [Masters Thesis]. Vilnius University; 2011. Available from: http://vddb.laba.lt/obj/LT-eLABa-0001:E.02~2008~D_20110709_152250-31963 ;

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


University of Illinois – Chicago

2. Pace, Wiktoria. Versatility of Ketonitrones in the Synthesis of Key C-C and C-N Bonds in Biologically Relevant Molecules.

Degree: 2016, University of Illinois – Chicago

 Our group’s development of N-O and C-N bonds via Chan-Lam coupling between oximes and boronic acids positioned us to discover N-aryl and N-vinyl ketonitrones. N-aryl… (more)

Subjects/Keywords: chemistry; rearrangement; organic

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pace, W. (2016). Versatility of Ketonitrones in the Synthesis of Key C-C and C-N Bonds in Biologically Relevant Molecules. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21258

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):

Pace, Wiktoria. “Versatility of Ketonitrones in the Synthesis of Key C-C and C-N Bonds in Biologically Relevant Molecules.” 2016. Thesis, University of Illinois – Chicago. Accessed October 23, 2019. http://hdl.handle.net/10027/21258.

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

MLA Handbook (7th Edition):

Pace, Wiktoria. “Versatility of Ketonitrones in the Synthesis of Key C-C and C-N Bonds in Biologically Relevant Molecules.” 2016. Web. 23 Oct 2019.

Vancouver:

Pace W. Versatility of Ketonitrones in the Synthesis of Key C-C and C-N Bonds in Biologically Relevant Molecules. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10027/21258.

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

Council of Science Editors:

Pace W. Versatility of Ketonitrones in the Synthesis of Key C-C and C-N Bonds in Biologically Relevant Molecules. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/21258

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


Princeton University

3. Clay, Derek. NOVEL GENETIC MANIPULATION APPROACHES TO INVESTIGATE GENOMIC REARRANGEMENT IN OXYTRICHA TRIFALLAX .

Degree: PhD, 2019, Princeton University

 The dual nuclear structure of ciliates, and the derivation of the somatic nucleus from the germline nucleus makes ciliates great model system for studying genomic… (more)

Subjects/Keywords: Ciliates; Genomic Rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Clay, D. (2019). NOVEL GENETIC MANIPULATION APPROACHES TO INVESTIGATE GENOMIC REARRANGEMENT IN OXYTRICHA TRIFALLAX . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01jq085n76p

Chicago Manual of Style (16th Edition):

Clay, Derek. “NOVEL GENETIC MANIPULATION APPROACHES TO INVESTIGATE GENOMIC REARRANGEMENT IN OXYTRICHA TRIFALLAX .” 2019. Doctoral Dissertation, Princeton University. Accessed October 23, 2019. http://arks.princeton.edu/ark:/88435/dsp01jq085n76p.

MLA Handbook (7th Edition):

Clay, Derek. “NOVEL GENETIC MANIPULATION APPROACHES TO INVESTIGATE GENOMIC REARRANGEMENT IN OXYTRICHA TRIFALLAX .” 2019. Web. 23 Oct 2019.

Vancouver:

Clay D. NOVEL GENETIC MANIPULATION APPROACHES TO INVESTIGATE GENOMIC REARRANGEMENT IN OXYTRICHA TRIFALLAX . [Internet] [Doctoral dissertation]. Princeton University; 2019. [cited 2019 Oct 23]. Available from: http://arks.princeton.edu/ark:/88435/dsp01jq085n76p.

Council of Science Editors:

Clay D. NOVEL GENETIC MANIPULATION APPROACHES TO INVESTIGATE GENOMIC REARRANGEMENT IN OXYTRICHA TRIFALLAX . [Doctoral Dissertation]. Princeton University; 2019. Available from: http://arks.princeton.edu/ark:/88435/dsp01jq085n76p


University of Vermont

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

Degree: PhD, Chemistry, 2014, University of Vermont

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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Yang, Yanbo. “Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement.” 2014. Doctoral Dissertation, University of Vermont. Accessed October 23, 2019. https://scholarworks.uvm.edu/graddis/261.

MLA Handbook (7th Edition):

Yang, Yanbo. “Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement.” 2014. Web. 23 Oct 2019.

Vancouver:

Yang Y. Pd0-Catalyzed Formal 1,3-Diaza-Claisen Rearrangement. Design And Development Of Cationic 1,3-Diaza-Claisen Rearrangement. [Internet] [Doctoral dissertation]. University of Vermont; 2014. [cited 2019 Oct 23]. Available from: https://scholarworks.uvm.edu/graddis/261.

Council of Science Editors:

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


University of Utah

5. Boyarskikh, Vyacheslav Vladimirovich. Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement.

Degree: PhD, Chemistry;, 2010, University of Utah

 Sulfonium ylides are formed using mild conditions and a diazo decomposition reaction catalyzed by a transition metal. These intermediates can undergo a variety of synthetically… (more)

Subjects/Keywords: Sigmatropic rearrangement; Stereoselective; Sulfonium ylide

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Boyarskikh, V. V. (2010). Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1242/rec/113

Chicago Manual of Style (16th Edition):

Boyarskikh, Vyacheslav Vladimirovich. “Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement.” 2010. Doctoral Dissertation, University of Utah. Accessed October 23, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1242/rec/113.

MLA Handbook (7th Edition):

Boyarskikh, Vyacheslav Vladimirovich. “Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement.” 2010. Web. 23 Oct 2019.

Vancouver:

Boyarskikh VV. Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2019 Oct 23]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1242/rec/113.

Council of Science Editors:

Boyarskikh VV. Approaches towards the stereoselective sulfonium ylide [3,3]-sigmatropic rearrangement. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1242/rec/113


University of Alberta

6. Stewart, Craig. Oxonium Ylide Rearrangements: A Novel Approach Towards the Synthesis of the Phorbol Skeleton.

Degree: PhD, Department of Chemistry, 2010, University of Alberta

 Oxonium ylides are highly reactive intermediates that can be used for the synthesis of heterocyclic and carbocyclic frameworks. These putative intermediates are almost exclusively formed… (more)

Subjects/Keywords: Phorbol; Stevens Rearrangement; Oxonium Ylide

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Stewart, C. (2010). Oxonium Ylide Rearrangements: A Novel Approach Towards the Synthesis of the Phorbol Skeleton. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/5712m8101

Chicago Manual of Style (16th Edition):

Stewart, Craig. “Oxonium Ylide Rearrangements: A Novel Approach Towards the Synthesis of the Phorbol Skeleton.” 2010. Doctoral Dissertation, University of Alberta. Accessed October 23, 2019. https://era.library.ualberta.ca/files/5712m8101.

MLA Handbook (7th Edition):

Stewart, Craig. “Oxonium Ylide Rearrangements: A Novel Approach Towards the Synthesis of the Phorbol Skeleton.” 2010. Web. 23 Oct 2019.

Vancouver:

Stewart C. Oxonium Ylide Rearrangements: A Novel Approach Towards the Synthesis of the Phorbol Skeleton. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2019 Oct 23]. Available from: https://era.library.ualberta.ca/files/5712m8101.

Council of Science Editors:

Stewart C. Oxonium Ylide Rearrangements: A Novel Approach Towards the Synthesis of the Phorbol Skeleton. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/5712m8101


Texas A&M University

7. Biswas, Bibaswan. Mechanistic Investigation of Rearrangement of Ammonium Ylides.

Degree: 2015, Texas A&M University

 A central aim of physical organic chemistry is the elucidation of reaction mechanisms. This knowledge is then usable in the rational control of reactions and… (more)

Subjects/Keywords: Sigmatropic rearrangement; Sommelet-Hauser; Stevens

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Biswas, B. (2015). Mechanistic Investigation of Rearrangement of Ammonium Ylides. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155561

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):

Biswas, Bibaswan. “Mechanistic Investigation of Rearrangement of Ammonium Ylides.” 2015. Thesis, Texas A&M University. Accessed October 23, 2019. http://hdl.handle.net/1969.1/155561.

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

MLA Handbook (7th Edition):

Biswas, Bibaswan. “Mechanistic Investigation of Rearrangement of Ammonium Ylides.” 2015. Web. 23 Oct 2019.

Vancouver:

Biswas B. Mechanistic Investigation of Rearrangement of Ammonium Ylides. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1969.1/155561.

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

Council of Science Editors:

Biswas B. Mechanistic Investigation of Rearrangement of Ammonium Ylides. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155561

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


University of Manchester

8. Tait, Michael Buchanan. α-Arylation of lithiated allylic and vinylic ureas.

Degree: PhD, 2014, University of Manchester

 Chiral amines are widespread in naturally occurring and synthetic bioactive molecules. However, it remains challenging to synthesise these molecules in an enantiopure form. Investigations within… (more)

Subjects/Keywords: 572; Carbolithaition; Rearrangement; Lithiation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tait, M. B. (2014). α-Arylation of lithiated allylic and vinylic ureas. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/aarylation-of-lithiated-allylic-and-vinylic-ureas(9403f676-5c28-49db-9b00-dc41a8977d16).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607419

Chicago Manual of Style (16th Edition):

Tait, Michael Buchanan. “α-Arylation of lithiated allylic and vinylic ureas.” 2014. Doctoral Dissertation, University of Manchester. Accessed October 23, 2019. https://www.research.manchester.ac.uk/portal/en/theses/aarylation-of-lithiated-allylic-and-vinylic-ureas(9403f676-5c28-49db-9b00-dc41a8977d16).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607419.

MLA Handbook (7th Edition):

Tait, Michael Buchanan. “α-Arylation of lithiated allylic and vinylic ureas.” 2014. Web. 23 Oct 2019.

Vancouver:

Tait MB. α-Arylation of lithiated allylic and vinylic ureas. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2019 Oct 23]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/aarylation-of-lithiated-allylic-and-vinylic-ureas(9403f676-5c28-49db-9b00-dc41a8977d16).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607419.

Council of Science Editors:

Tait MB. α-Arylation of lithiated allylic and vinylic ureas. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/aarylation-of-lithiated-allylic-and-vinylic-ureas(9403f676-5c28-49db-9b00-dc41a8977d16).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.607419


Oregon State University

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

Degree: PhD, Chemistry, 1966, Oregon State University

Subjects/Keywords: Claisen rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Schatz, Bruce Stewart. “Kinetic studies of some thermal rearrangements.” 1966. Doctoral Dissertation, Oregon State University. Accessed October 23, 2019. http://hdl.handle.net/1957/47082.

MLA Handbook (7th Edition):

Schatz, Bruce Stewart. “Kinetic studies of some thermal rearrangements.” 1966. Web. 23 Oct 2019.

Vancouver:

Schatz BS. Kinetic studies of some thermal rearrangements. [Internet] [Doctoral dissertation]. Oregon State University; 1966. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1957/47082.

Council of Science Editors:

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


University of Manchester

10. Rabet, Pauline. New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks.

Degree: 2018, University of Manchester

 Nitrogen based functional groups are a recurrent motif in most natural products, pharmaceuticals and organic compounds in general. There is therefore a real interest in… (more)

Subjects/Keywords: Nitrogen; Catalyst; Photoredox; Rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rabet, P. (2018). New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313345

Chicago Manual of Style (16th Edition):

Rabet, Pauline. “New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks.” 2018. Doctoral Dissertation, University of Manchester. Accessed October 23, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313345.

MLA Handbook (7th Edition):

Rabet, Pauline. “New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks.” 2018. Web. 23 Oct 2019.

Vancouver:

Rabet P. New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2019 Oct 23]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313345.

Council of Science Editors:

Rabet P. New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313345


Boston College

11. Heusser, Carolyn Andrea. Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement.

Degree: MS, Chemistry, 2013, Boston College

 Chapter 1: There are a limited number of examples of metal-catalyzed Brook rearrangements in the literature, none of which involve ruthenium, rhodium, or iridium which… (more)

Subjects/Keywords: Acylsilane; Brook rearrangement; Cross Coupling

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Heusser, C. A. (2013). Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101169

Chicago Manual of Style (16th Edition):

Heusser, Carolyn Andrea. “Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement.” 2013. Masters Thesis, Boston College. Accessed October 23, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101169.

MLA Handbook (7th Edition):

Heusser, Carolyn Andrea. “Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement.” 2013. Web. 23 Oct 2019.

Vancouver:

Heusser CA. Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement. [Internet] [Masters thesis]. Boston College; 2013. [cited 2019 Oct 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101169.

Council of Science Editors:

Heusser CA. Efforts Towards the Cross Coupling of Acylsilanes and Electrophiles via a Metal-Catalyzed Brook Rearrangement. [Masters Thesis]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101169


University of Manchester

12. Rabet, Pauline. New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks.

Degree: PhD, 2018, University of Manchester

 Nitrogen based functional groups are a recurrent motif in most natural products, pharmaceuticals and organic compounds in general. There is therefore a real interest in… (more)

Subjects/Keywords: Nitrogen; Catalyst; Photoredox; Rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rabet, P. (2018). New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/new-methodologies-for-incorporation-of-nitrogen-based-functional-groups-onto-carbon-frameworks(b5ba1784-1341-4c2e-b4eb-53c3c1729c55).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771404

Chicago Manual of Style (16th Edition):

Rabet, Pauline. “New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks.” 2018. Doctoral Dissertation, University of Manchester. Accessed October 23, 2019. https://www.research.manchester.ac.uk/portal/en/theses/new-methodologies-for-incorporation-of-nitrogen-based-functional-groups-onto-carbon-frameworks(b5ba1784-1341-4c2e-b4eb-53c3c1729c55).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771404.

MLA Handbook (7th Edition):

Rabet, Pauline. “New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks.” 2018. Web. 23 Oct 2019.

Vancouver:

Rabet P. New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2019 Oct 23]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/new-methodologies-for-incorporation-of-nitrogen-based-functional-groups-onto-carbon-frameworks(b5ba1784-1341-4c2e-b4eb-53c3c1729c55).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771404.

Council of Science Editors:

Rabet P. New methodologies for incorporation of nitrogen based functional groups onto carbon frameworks. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/new-methodologies-for-incorporation-of-nitrogen-based-functional-groups-onto-carbon-frameworks(b5ba1784-1341-4c2e-b4eb-53c3c1729c55).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771404


Loughborough University

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

Degree: PhD, 2012, Loughborough University

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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Garcia-Torres, J. (2012). Development of a dual Fries-Claisen rearrangement strategy. (Doctoral Dissertation). Loughborough University. Retrieved from https://dspace.lboro.ac.uk/2134/11002 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.561193

Chicago Manual of Style (16th Edition):

Garcia-Torres, Jason. “Development of a dual Fries-Claisen rearrangement strategy.” 2012. Doctoral Dissertation, Loughborough University. Accessed October 23, 2019. https://dspace.lboro.ac.uk/2134/11002 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.561193.

MLA Handbook (7th Edition):

Garcia-Torres, Jason. “Development of a dual Fries-Claisen rearrangement strategy.” 2012. Web. 23 Oct 2019.

Vancouver:

Garcia-Torres J. Development of a dual Fries-Claisen rearrangement strategy. [Internet] [Doctoral dissertation]. Loughborough University; 2012. [cited 2019 Oct 23]. Available from: https://dspace.lboro.ac.uk/2134/11002 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.561193.

Council of Science Editors:

Garcia-Torres J. Development of a dual Fries-Claisen rearrangement strategy. [Doctoral Dissertation]. Loughborough University; 2012. Available from: https://dspace.lboro.ac.uk/2134/11002 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.561193


Loughborough University

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

Degree: PhD, 2012, Loughborough University

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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Garcia-Torres, Jason. “Development of a dual Fries-Claisen rearrangement strategy.” 2012. Doctoral Dissertation, Loughborough University. Accessed October 23, 2019. http://hdl.handle.net/2134/11002.

MLA Handbook (7th Edition):

Garcia-Torres, Jason. “Development of a dual Fries-Claisen rearrangement strategy.” 2012. Web. 23 Oct 2019.

Vancouver:

Garcia-Torres J. Development of a dual Fries-Claisen rearrangement strategy. [Internet] [Doctoral dissertation]. Loughborough University; 2012. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2134/11002.

Council of Science Editors:

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


University of Alberta

15. Johnston, Jeffrey. Synthetic Studies Towards (+)-Dactylol Utilizing an Oxonium Ylide Rearrangement and Related Studies.

Degree: PhD, Department of Chemistry, 2012, University of Alberta

 Dactylol is a structurally interesting sesquiterpene natural product. One of its key structural features is an the eight-membered ring. The challenges of synthesizing an eight… (more)

Subjects/Keywords: DDC; carbodiimide; oxonium ylide; dactylol; rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Johnston, J. (2012). Synthetic Studies Towards (+)-Dactylol Utilizing an Oxonium Ylide Rearrangement and Related Studies. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/5x21tg40c

Chicago Manual of Style (16th Edition):

Johnston, Jeffrey. “Synthetic Studies Towards (+)-Dactylol Utilizing an Oxonium Ylide Rearrangement and Related Studies.” 2012. Doctoral Dissertation, University of Alberta. Accessed October 23, 2019. https://era.library.ualberta.ca/files/5x21tg40c.

MLA Handbook (7th Edition):

Johnston, Jeffrey. “Synthetic Studies Towards (+)-Dactylol Utilizing an Oxonium Ylide Rearrangement and Related Studies.” 2012. Web. 23 Oct 2019.

Vancouver:

Johnston J. Synthetic Studies Towards (+)-Dactylol Utilizing an Oxonium Ylide Rearrangement and Related Studies. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2019 Oct 23]. Available from: https://era.library.ualberta.ca/files/5x21tg40c.

Council of Science Editors:

Johnston J. Synthetic Studies Towards (+)-Dactylol Utilizing an Oxonium Ylide Rearrangement and Related Studies. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/5x21tg40c


University of Tasmania

16. Howard, JK. New methods for the synthesis of nitrogen containing, biologically relevant small molecules.

Degree: 2015, University of Tasmania

 The following thesis consists of two independent parts, both linked by a common theme of developing new methods for the synthesis of small nitrogen containing… (more)

Subjects/Keywords: Pyrrole; Cyclopropene; Oxidation; Rearrangement; Pyrrolinone; Photochemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Howard, J. (2015). New methods for the synthesis of nitrogen containing, biologically relevant small molecules. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/22887/1/Howard_whole_thesis.pdf

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):

Howard, JK. “New methods for the synthesis of nitrogen containing, biologically relevant small molecules.” 2015. Thesis, University of Tasmania. Accessed October 23, 2019. https://eprints.utas.edu.au/22887/1/Howard_whole_thesis.pdf.

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

MLA Handbook (7th Edition):

Howard, JK. “New methods for the synthesis of nitrogen containing, biologically relevant small molecules.” 2015. Web. 23 Oct 2019.

Vancouver:

Howard J. New methods for the synthesis of nitrogen containing, biologically relevant small molecules. [Internet] [Thesis]. University of Tasmania; 2015. [cited 2019 Oct 23]. Available from: https://eprints.utas.edu.au/22887/1/Howard_whole_thesis.pdf.

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

Council of Science Editors:

Howard J. New methods for the synthesis of nitrogen containing, biologically relevant small molecules. [Thesis]. University of Tasmania; 2015. Available from: https://eprints.utas.edu.au/22887/1/Howard_whole_thesis.pdf

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


Youngstown State University

17. Copeland, Christopher N., II. Modified Conditions for Acyl Azide and Carbamate Synthesis.

Degree: MSin Chemistry, Department of Chemistry, 2016, Youngstown State University

 Carbamate chemistry has a wide variety of applications both in synthetic chemistry as well as in biology. This carbon-nitrogen containing functional group is used as… (more)

Subjects/Keywords: Chemistry; Organic Chemistry; Azides; Carbamates; Curtius rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Copeland, Christopher N., I. (2016). Modified Conditions for Acyl Azide and Carbamate Synthesis. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178

Chicago Manual of Style (16th Edition):

Copeland, Christopher N., II. “Modified Conditions for Acyl Azide and Carbamate Synthesis.” 2016. Masters Thesis, Youngstown State University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178.

MLA Handbook (7th Edition):

Copeland, Christopher N., II. “Modified Conditions for Acyl Azide and Carbamate Synthesis.” 2016. Web. 23 Oct 2019.

Vancouver:

Copeland, Christopher N. I. Modified Conditions for Acyl Azide and Carbamate Synthesis. [Internet] [Masters thesis]. Youngstown State University; 2016. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178.

Council of Science Editors:

Copeland, Christopher N. I. Modified Conditions for Acyl Azide and Carbamate Synthesis. [Masters Thesis]. Youngstown State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1473765784542178


University of California – Riverside

18. Moehlig, Melissa Padilla. Towards a Catalytic Asymmetric Cope Rearrangement and the Synthesis and Self-Assembly of Metal-Coordinated Hosts.

Degree: Chemistry, 2013, University of California – Riverside

 The Cope rearrangement has been used as the key step of several natural products but to date there is only one limited example in the… (more)

Subjects/Keywords: Organic chemistry; biomimetic; catalysis; Cope rearrangement; oxidation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Moehlig, M. P. (2013). Towards a Catalytic Asymmetric Cope Rearrangement and the Synthesis and Self-Assembly of Metal-Coordinated Hosts. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/4gc654st

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):

Moehlig, Melissa Padilla. “Towards a Catalytic Asymmetric Cope Rearrangement and the Synthesis and Self-Assembly of Metal-Coordinated Hosts.” 2013. Thesis, University of California – Riverside. Accessed October 23, 2019. http://www.escholarship.org/uc/item/4gc654st.

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

MLA Handbook (7th Edition):

Moehlig, Melissa Padilla. “Towards a Catalytic Asymmetric Cope Rearrangement and the Synthesis and Self-Assembly of Metal-Coordinated Hosts.” 2013. Web. 23 Oct 2019.

Vancouver:

Moehlig MP. Towards a Catalytic Asymmetric Cope Rearrangement and the Synthesis and Self-Assembly of Metal-Coordinated Hosts. [Internet] [Thesis]. University of California – Riverside; 2013. [cited 2019 Oct 23]. Available from: http://www.escholarship.org/uc/item/4gc654st.

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

Council of Science Editors:

Moehlig MP. Towards a Catalytic Asymmetric Cope Rearrangement and the Synthesis and Self-Assembly of Metal-Coordinated Hosts. [Thesis]. University of California – Riverside; 2013. Available from: http://www.escholarship.org/uc/item/4gc654st

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


University of Illinois – Chicago

19. Wang, Heng-Yen. Carbon–Carbon, Carbon–Oxygen, or Carbon–Nitrogen Bond Formation via 3,3- or 1,3-Rearrangements of O-Vinyl.

Degree: 2014, University of Illinois – Chicago

 Rearrangements of N–O bonds have been employed in the development of new methods for the preparation highly functionalized molecules. Specifically, [1,3]- and [3,3]-rearrangements of O-vinyl… (more)

Subjects/Keywords: oxime; rearrangement; pyrrole; O-vinyl; isomerization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, H. (2014). Carbon–Carbon, Carbon–Oxygen, or Carbon–Nitrogen Bond Formation via 3,3- or 1,3-Rearrangements of O-Vinyl. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/11299

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):

Wang, Heng-Yen. “Carbon–Carbon, Carbon–Oxygen, or Carbon–Nitrogen Bond Formation via 3,3- or 1,3-Rearrangements of O-Vinyl.” 2014. Thesis, University of Illinois – Chicago. Accessed October 23, 2019. http://hdl.handle.net/10027/11299.

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

MLA Handbook (7th Edition):

Wang, Heng-Yen. “Carbon–Carbon, Carbon–Oxygen, or Carbon–Nitrogen Bond Formation via 3,3- or 1,3-Rearrangements of O-Vinyl.” 2014. Web. 23 Oct 2019.

Vancouver:

Wang H. Carbon–Carbon, Carbon–Oxygen, or Carbon–Nitrogen Bond Formation via 3,3- or 1,3-Rearrangements of O-Vinyl. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10027/11299.

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

Council of Science Editors:

Wang H. Carbon–Carbon, Carbon–Oxygen, or Carbon–Nitrogen Bond Formation via 3,3- or 1,3-Rearrangements of O-Vinyl. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/11299

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

20. Shieh, Wan-Yi: Annie). Analysis of DIE5 and LIA5 reveals the importance of DNA repair in programmed DNA rearrangement of Tetrahymena thermophila.

Degree: PhD, Biology and Biomedical Sciences: Developmental, Regenerative and Stem Cell Biology, 2012, Washington University in St. Louis

  During its somatic nuclear differentiation, the single cell eukaryote Tetrahymena thermophila undergoes genome-wide programmed DNA rearrangement to eliminate transposon-like elements from its future soma.… (more)

Subjects/Keywords: DIE5; DNA rearrangement; Epigenetics; LIA5; Tetrahymena

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shieh, W. A. (2012). Analysis of DIE5 and LIA5 reveals the importance of DNA repair in programmed DNA rearrangement of Tetrahymena thermophila. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/978

Chicago Manual of Style (16th Edition):

Shieh, Wan-Yi: Annie). “Analysis of DIE5 and LIA5 reveals the importance of DNA repair in programmed DNA rearrangement of Tetrahymena thermophila.” 2012. Doctoral Dissertation, Washington University in St. Louis. Accessed October 23, 2019. https://openscholarship.wustl.edu/etd/978.

MLA Handbook (7th Edition):

Shieh, Wan-Yi: Annie). “Analysis of DIE5 and LIA5 reveals the importance of DNA repair in programmed DNA rearrangement of Tetrahymena thermophila.” 2012. Web. 23 Oct 2019.

Vancouver:

Shieh WA. Analysis of DIE5 and LIA5 reveals the importance of DNA repair in programmed DNA rearrangement of Tetrahymena thermophila. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2012. [cited 2019 Oct 23]. Available from: https://openscholarship.wustl.edu/etd/978.

Council of Science Editors:

Shieh WA. Analysis of DIE5 and LIA5 reveals the importance of DNA repair in programmed DNA rearrangement of Tetrahymena thermophila. [Doctoral Dissertation]. Washington University in St. Louis; 2012. Available from: https://openscholarship.wustl.edu/etd/978


University of Manchester

21. Overy, Anthony Jason. Cyclic and Spirocyclic α-Tertiary Amines by Organolithium Rearrangement.

Degree: 2015, University of Manchester

Spirocyclic & cyclic α-tertiary amines are frequently found in naturally occurring biological and synthetic molecules. Synthetic methods which allow the concise synthesis of such molecules… (more)

Subjects/Keywords: Spirocyclic; α-tertiary amines; Organolithium Rearrangement; Cyclic

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Overy, A. J. (2015). Cyclic and Spirocyclic α-Tertiary Amines by Organolithium Rearrangement. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:245070

Chicago Manual of Style (16th Edition):

Overy, Anthony Jason. “Cyclic and Spirocyclic α-Tertiary Amines by Organolithium Rearrangement.” 2015. Doctoral Dissertation, University of Manchester. Accessed October 23, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:245070.

MLA Handbook (7th Edition):

Overy, Anthony Jason. “Cyclic and Spirocyclic α-Tertiary Amines by Organolithium Rearrangement.” 2015. Web. 23 Oct 2019.

Vancouver:

Overy AJ. Cyclic and Spirocyclic α-Tertiary Amines by Organolithium Rearrangement. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Oct 23]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:245070.

Council of Science Editors:

Overy AJ. Cyclic and Spirocyclic α-Tertiary Amines by Organolithium Rearrangement. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:245070

22. Richoux Jr, Gary Michael. Enantioselective Synthesis of Drug-like Molecules via Axially-Chiral Intermediates.

Degree: PhD, Chemistry, 2016, Virginia Tech

 The self-regeneration of stereocenters via stereolabile axially-chiral intermediates (SRSvSACI) is a synthetic strategy in which the configuration of a starting material, possessing only a single… (more)

Subjects/Keywords: Memory of Chirality; benzodiazepine; rearrangement; SRSvSACI

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Richoux Jr, G. M. (2016). Enantioselective Synthesis of Drug-like Molecules via Axially-Chiral Intermediates. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/71675

Chicago Manual of Style (16th Edition):

Richoux Jr, Gary Michael. “Enantioselective Synthesis of Drug-like Molecules via Axially-Chiral Intermediates.” 2016. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/71675.

MLA Handbook (7th Edition):

Richoux Jr, Gary Michael. “Enantioselective Synthesis of Drug-like Molecules via Axially-Chiral Intermediates.” 2016. Web. 23 Oct 2019.

Vancouver:

Richoux Jr GM. Enantioselective Synthesis of Drug-like Molecules via Axially-Chiral Intermediates. [Internet] [Doctoral dissertation]. Virginia Tech; 2016. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/71675.

Council of Science Editors:

Richoux Jr GM. Enantioselective Synthesis of Drug-like Molecules via Axially-Chiral Intermediates. [Doctoral Dissertation]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/71675


Virginia Tech

23. Chen, Xiaofeng. Plane Permutations and their Applications to Graph Embeddings and Genome Rearrangements.

Degree: PhD, Mathematics, 2017, Virginia Tech

 Maps have been extensively studied and are important in many research fields. A map is a 2-cell embedding of a graph on an orientable surface.… (more)

Subjects/Keywords: Plane Permutation; Map; Graph Embedding; Genome Rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, X. (2017). Plane Permutations and their Applications to Graph Embeddings and Genome Rearrangements. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77535

Chicago Manual of Style (16th Edition):

Chen, Xiaofeng. “Plane Permutations and their Applications to Graph Embeddings and Genome Rearrangements.” 2017. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/77535.

MLA Handbook (7th Edition):

Chen, Xiaofeng. “Plane Permutations and their Applications to Graph Embeddings and Genome Rearrangements.” 2017. Web. 23 Oct 2019.

Vancouver:

Chen X. Plane Permutations and their Applications to Graph Embeddings and Genome Rearrangements. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/77535.

Council of Science Editors:

Chen X. Plane Permutations and their Applications to Graph Embeddings and Genome Rearrangements. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/77535


University of St. Andrews

24. Joannesse, Caroline. Isothiourea-promoted O- to C-carboxyl transfer reactions .

Degree: 2011, University of St. Andrews

 This thesis describes an extensive investigation of the O- to C-carboxyl transfer of oxazolyl carbonates using isothioureas as Lewis base catalysts. The structural requirements of… (more)

Subjects/Keywords: Organocatalysis; Isothiourea; Asymmetric catalysis; Steglich rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Joannesse, C. (2011). Isothiourea-promoted O- to C-carboxyl transfer reactions . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/3109

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):

Joannesse, Caroline. “Isothiourea-promoted O- to C-carboxyl transfer reactions .” 2011. Thesis, University of St. Andrews. Accessed October 23, 2019. http://hdl.handle.net/10023/3109.

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

MLA Handbook (7th Edition):

Joannesse, Caroline. “Isothiourea-promoted O- to C-carboxyl transfer reactions .” 2011. Web. 23 Oct 2019.

Vancouver:

Joannesse C. Isothiourea-promoted O- to C-carboxyl transfer reactions . [Internet] [Thesis]. University of St. Andrews; 2011. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10023/3109.

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

Council of Science Editors:

Joannesse C. Isothiourea-promoted O- to C-carboxyl transfer reactions . [Thesis]. University of St. Andrews; 2011. Available from: http://hdl.handle.net/10023/3109

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


University of Wollongong

25. Mao, Meng. Mitochondrial genomes and their utility for the recovery of phylogeny in the Hymenoptera.

Degree: PhD, 2014, University of Wollongong

  The Hymenoptera, comprising of sawflies, wasps, bees and ants, is the third largest order of insects. It contains more than 155,000 described species, placed… (more)

Subjects/Keywords: Mitochondrial genome; Hymenoptera; gene rearrangement; phylogeny

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mao, M. (2014). Mitochondrial genomes and their utility for the recovery of phylogeny in the Hymenoptera. (Doctoral Dissertation). University of Wollongong. Retrieved from ; https://ro.uow.edu.au/theses/4206

Chicago Manual of Style (16th Edition):

Mao, Meng. “Mitochondrial genomes and their utility for the recovery of phylogeny in the Hymenoptera.” 2014. Doctoral Dissertation, University of Wollongong. Accessed October 23, 2019. ; https://ro.uow.edu.au/theses/4206.

MLA Handbook (7th Edition):

Mao, Meng. “Mitochondrial genomes and their utility for the recovery of phylogeny in the Hymenoptera.” 2014. Web. 23 Oct 2019.

Vancouver:

Mao M. Mitochondrial genomes and their utility for the recovery of phylogeny in the Hymenoptera. [Internet] [Doctoral dissertation]. University of Wollongong; 2014. [cited 2019 Oct 23]. Available from: ; https://ro.uow.edu.au/theses/4206.

Council of Science Editors:

Mao M. Mitochondrial genomes and their utility for the recovery of phylogeny in the Hymenoptera. [Doctoral Dissertation]. University of Wollongong; 2014. Available from: ; https://ro.uow.edu.au/theses/4206


University of Illinois – Urbana-Champaign

26. Berdan, Emma. Linking ecological divergence and reproductive isolation: a tale of two killifish.

Degree: PhD, 0314, 2012, University of Illinois – Urbana-Champaign

 Gene flow and recombination directly oppose genetic differentiation and speciation because they homogenize allele combinations that are unique to each population/species (Felsenstein 1981; Rieseberg 2001;… (more)

Subjects/Keywords: Speciation; reinforcement; chromosomal rearrangement; linkage disequilibrium

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Berdan, E. (2012). Linking ecological divergence and reproductive isolation: a tale of two killifish. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/34468

Chicago Manual of Style (16th Edition):

Berdan, Emma. “Linking ecological divergence and reproductive isolation: a tale of two killifish.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 23, 2019. http://hdl.handle.net/2142/34468.

MLA Handbook (7th Edition):

Berdan, Emma. “Linking ecological divergence and reproductive isolation: a tale of two killifish.” 2012. Web. 23 Oct 2019.

Vancouver:

Berdan E. Linking ecological divergence and reproductive isolation: a tale of two killifish. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2142/34468.

Council of Science Editors:

Berdan E. Linking ecological divergence and reproductive isolation: a tale of two killifish. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/34468


University of South Carolina

27. Yang, Yiting. Genome Rearrangement, Randic Index and Routing Number.

Degree: PhD, Mathematics, 2010, University of South Carolina

  This dissertation mainly consists of the results of one published [43], three submitted papers [29-31] and two manuscripts [42, 48]. Three kinds of applied… (more)

Subjects/Keywords: Genome rearrangement; Randic index; Routing number

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yang, Y. (2010). Genome Rearrangement, Randic Index and Routing Number. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/425

Chicago Manual of Style (16th Edition):

Yang, Yiting. “Genome Rearrangement, Randic Index and Routing Number.” 2010. Doctoral Dissertation, University of South Carolina. Accessed October 23, 2019. https://scholarcommons.sc.edu/etd/425.

MLA Handbook (7th Edition):

Yang, Yiting. “Genome Rearrangement, Randic Index and Routing Number.” 2010. Web. 23 Oct 2019.

Vancouver:

Yang Y. Genome Rearrangement, Randic Index and Routing Number. [Internet] [Doctoral dissertation]. University of South Carolina; 2010. [cited 2019 Oct 23]. Available from: https://scholarcommons.sc.edu/etd/425.

Council of Science Editors:

Yang Y. Genome Rearrangement, Randic Index and Routing Number. [Doctoral Dissertation]. University of South Carolina; 2010. Available from: https://scholarcommons.sc.edu/etd/425


University of Notre Dame

28. Kyle Chormanski. Alkyne Substituent Effects in Radicals and Carbocations</h1>.

Degree: MS, Chemistry and Biochemistry, 2010, University of Notre Dame

  Alkyne substituent effects in the methylenecyclopropane rearrangement as well as solvolysis studies of the structurally similar trifluoroacetates were determined. The results of these kinetic… (more)

Subjects/Keywords: kinetics; sigma scale; Methylenecyclopropane rearrangement; rate study

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chormanski, K. (2010). Alkyne Substituent Effects in Radicals and Carbocations</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/n583xs57z1t

Chicago Manual of Style (16th Edition):

Chormanski, Kyle. “Alkyne Substituent Effects in Radicals and Carbocations</h1>.” 2010. Masters Thesis, University of Notre Dame. Accessed October 23, 2019. https://curate.nd.edu/show/n583xs57z1t.

MLA Handbook (7th Edition):

Chormanski, Kyle. “Alkyne Substituent Effects in Radicals and Carbocations</h1>.” 2010. Web. 23 Oct 2019.

Vancouver:

Chormanski K. Alkyne Substituent Effects in Radicals and Carbocations</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2010. [cited 2019 Oct 23]. Available from: https://curate.nd.edu/show/n583xs57z1t.

Council of Science Editors:

Chormanski K. Alkyne Substituent Effects in Radicals and Carbocations</h1>. [Masters Thesis]. University of Notre Dame; 2010. Available from: https://curate.nd.edu/show/n583xs57z1t


University of New South Wales

29. Qu, Ji. New cyclization reactions of indoles.

Degree: Chemistry, 2010, University of New South Wales

 The thesis is mainly concerned with the development of synthetic strategies for the synthesis of new heterocyclic systems based on indoles, and which are related… (more)

Subjects/Keywords: Beckmann rearrangement; Indole; Cyclization; Imidazole; Indolobenzodiazepine

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Qu, J. (2010). New cyclization reactions of indoles. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/45090 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8385/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Qu, Ji. “New cyclization reactions of indoles.” 2010. Doctoral Dissertation, University of New South Wales. Accessed October 23, 2019. http://handle.unsw.edu.au/1959.4/45090 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8385/SOURCE02?view=true.

MLA Handbook (7th Edition):

Qu, Ji. “New cyclization reactions of indoles.” 2010. Web. 23 Oct 2019.

Vancouver:

Qu J. New cyclization reactions of indoles. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Oct 23]. Available from: http://handle.unsw.edu.au/1959.4/45090 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8385/SOURCE02?view=true.

Council of Science Editors:

Qu J. New cyclization reactions of indoles. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/45090 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8385/SOURCE02?view=true

30. Veits, Gesine. Harnessing the Power of Furfuryl Cations: The Aza-Piancatelli Rearrangement and Beyond.

Degree: 2014, University of California – eScholarship, University of California

 Harnessing the Power of Furfuryl Cations:The Aza-Piancatelli Rearrangement and BeyondbyGesine Kerstin VeitsThe ubiquity of amine functional groups in all of nature as well as a… (more)

Subjects/Keywords: Chemistry; Aza-Piancatelli; Dysprosium; Furan; Rearrangement

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Veits, G. (2014). Harnessing the Power of Furfuryl Cations: The Aza-Piancatelli Rearrangement and Beyond. (Thesis). University of California – eScholarship, University of California. Retrieved from http://www.escholarship.org/uc/item/8v42p9wz

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):

Veits, Gesine. “Harnessing the Power of Furfuryl Cations: The Aza-Piancatelli Rearrangement and Beyond.” 2014. Thesis, University of California – eScholarship, University of California. Accessed October 23, 2019. http://www.escholarship.org/uc/item/8v42p9wz.

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

MLA Handbook (7th Edition):

Veits, Gesine. “Harnessing the Power of Furfuryl Cations: The Aza-Piancatelli Rearrangement and Beyond.” 2014. Web. 23 Oct 2019.

Vancouver:

Veits G. Harnessing the Power of Furfuryl Cations: The Aza-Piancatelli Rearrangement and Beyond. [Internet] [Thesis]. University of California – eScholarship, University of California; 2014. [cited 2019 Oct 23]. Available from: http://www.escholarship.org/uc/item/8v42p9wz.

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

Council of Science Editors:

Veits G. Harnessing the Power of Furfuryl Cations: The Aza-Piancatelli Rearrangement and Beyond. [Thesis]. University of California – eScholarship, University of California; 2014. Available from: http://www.escholarship.org/uc/item/8v42p9wz

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

[1] [2] [3] [4] [5] … [12]

.