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You searched for subject:(Lactones). Showing records 1 – 30 of 228 total matches.

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Oregon State University

1. Wyatt, Carolyn Jane. Lactone precursor in milk fat.

Degree: PhD, Food Science and Technology, 1966, Oregon State University

Subjects/Keywords: Lactones

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APA (6th Edition):

Wyatt, C. J. (1966). Lactone precursor in milk fat. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/27010

Chicago Manual of Style (16th Edition):

Wyatt, Carolyn Jane. “Lactone precursor in milk fat.” 1966. Doctoral Dissertation, Oregon State University. Accessed December 02, 2020. http://hdl.handle.net/1957/27010.

MLA Handbook (7th Edition):

Wyatt, Carolyn Jane. “Lactone precursor in milk fat.” 1966. Web. 02 Dec 2020.

Vancouver:

Wyatt CJ. Lactone precursor in milk fat. [Internet] [Doctoral dissertation]. Oregon State University; 1966. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1957/27010.

Council of Science Editors:

Wyatt CJ. Lactone precursor in milk fat. [Doctoral Dissertation]. Oregon State University; 1966. Available from: http://hdl.handle.net/1957/27010


University of Adelaide

2. Babidge, Peter John. Synthesis and reaction of enol-lactones / by Peter J. Babidge.

Degree: 1979, University of Adelaide

Subjects/Keywords: Lactones.

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APA (6th Edition):

Babidge, P. J. (1979). Synthesis and reaction of enol-lactones / by Peter J. Babidge. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/19965

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):

Babidge, Peter John. “Synthesis and reaction of enol-lactones / by Peter J. Babidge.” 1979. Thesis, University of Adelaide. Accessed December 02, 2020. http://hdl.handle.net/2440/19965.

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

MLA Handbook (7th Edition):

Babidge, Peter John. “Synthesis and reaction of enol-lactones / by Peter J. Babidge.” 1979. Web. 02 Dec 2020.

Vancouver:

Babidge PJ. Synthesis and reaction of enol-lactones / by Peter J. Babidge. [Internet] [Thesis]. University of Adelaide; 1979. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/2440/19965.

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

Council of Science Editors:

Babidge PJ. Synthesis and reaction of enol-lactones / by Peter J. Babidge. [Thesis]. University of Adelaide; 1979. Available from: http://hdl.handle.net/2440/19965

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


University of Adelaide

3. Hancock, William Stephen. Approaches towards the synthesis of rosenonolactone.

Degree: 1969, University of Adelaide

Subjects/Keywords: Lactones.

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APA (6th Edition):

Hancock, W. S. (1969). Approaches towards the synthesis of rosenonolactone. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/20107

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):

Hancock, William Stephen. “Approaches towards the synthesis of rosenonolactone.” 1969. Thesis, University of Adelaide. Accessed December 02, 2020. http://hdl.handle.net/2440/20107.

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

MLA Handbook (7th Edition):

Hancock, William Stephen. “Approaches towards the synthesis of rosenonolactone.” 1969. Web. 02 Dec 2020.

Vancouver:

Hancock WS. Approaches towards the synthesis of rosenonolactone. [Internet] [Thesis]. University of Adelaide; 1969. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/2440/20107.

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

Council of Science Editors:

Hancock WS. Approaches towards the synthesis of rosenonolactone. [Thesis]. University of Adelaide; 1969. Available from: http://hdl.handle.net/2440/20107

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


Oregon State University

4. Giesbrecht, Heath Eugene. Broadening the scope of the modified-Julia reaction : a mild and stereoselective method for the synthesis of (Z)-configurated α,β-unsaturated lactones.

Degree: MS, Chemistry, 2008, Oregon State University

 An intramolecular variant of the modified-Julia olefination was demonstrated by the synthesis of α,β-unsaturated lactones in a mild and (Z)-selective fashion. The lynchpin reagent (benzothiazol-2-sulfonyl)… (more)

Subjects/Keywords: Olefination; Lactones  – Synthesis

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APA (6th Edition):

Giesbrecht, H. E. (2008). Broadening the scope of the modified-Julia reaction : a mild and stereoselective method for the synthesis of (Z)-configurated α,β-unsaturated lactones. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/8943

Chicago Manual of Style (16th Edition):

Giesbrecht, Heath Eugene. “Broadening the scope of the modified-Julia reaction : a mild and stereoselective method for the synthesis of (Z)-configurated α,β-unsaturated lactones.” 2008. Masters Thesis, Oregon State University. Accessed December 02, 2020. http://hdl.handle.net/1957/8943.

MLA Handbook (7th Edition):

Giesbrecht, Heath Eugene. “Broadening the scope of the modified-Julia reaction : a mild and stereoselective method for the synthesis of (Z)-configurated α,β-unsaturated lactones.” 2008. Web. 02 Dec 2020.

Vancouver:

Giesbrecht HE. Broadening the scope of the modified-Julia reaction : a mild and stereoselective method for the synthesis of (Z)-configurated α,β-unsaturated lactones. [Internet] [Masters thesis]. Oregon State University; 2008. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1957/8943.

Council of Science Editors:

Giesbrecht HE. Broadening the scope of the modified-Julia reaction : a mild and stereoselective method for the synthesis of (Z)-configurated α,β-unsaturated lactones. [Masters Thesis]. Oregon State University; 2008. Available from: http://hdl.handle.net/1957/8943


Vanderbilt University

5. Flach, Andrew Louis. Investigation of Counterion Effects in an Organocatalyzed Iodolactonization and Discovery of an Organocatalyzed Iodolactonization to Give 7-Membered Lactones.

Degree: MS, Chemistry, 2017, Vanderbilt University

 Iodolactonization is a venerable chemical reaction with considerable utility in the synthesis of organic compounds. More recently, enantioselective methods reliant upon organocatalysts have been developed.… (more)

Subjects/Keywords: Iodolactones; Halolactonization; Lactones; Iodolactonization; Counterions

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APA (6th Edition):

Flach, A. L. (2017). Investigation of Counterion Effects in an Organocatalyzed Iodolactonization and Discovery of an Organocatalyzed Iodolactonization to Give 7-Membered Lactones. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14013

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):

Flach, Andrew Louis. “Investigation of Counterion Effects in an Organocatalyzed Iodolactonization and Discovery of an Organocatalyzed Iodolactonization to Give 7-Membered Lactones.” 2017. Thesis, Vanderbilt University. Accessed December 02, 2020. http://hdl.handle.net/1803/14013.

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

MLA Handbook (7th Edition):

Flach, Andrew Louis. “Investigation of Counterion Effects in an Organocatalyzed Iodolactonization and Discovery of an Organocatalyzed Iodolactonization to Give 7-Membered Lactones.” 2017. Web. 02 Dec 2020.

Vancouver:

Flach AL. Investigation of Counterion Effects in an Organocatalyzed Iodolactonization and Discovery of an Organocatalyzed Iodolactonization to Give 7-Membered Lactones. [Internet] [Thesis]. Vanderbilt University; 2017. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1803/14013.

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

Council of Science Editors:

Flach AL. Investigation of Counterion Effects in an Organocatalyzed Iodolactonization and Discovery of an Organocatalyzed Iodolactonization to Give 7-Membered Lactones. [Thesis]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/14013

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


Drexel University

6. Gupta, Ashutosh. Development of detailed, reduced and skeletal kinetic mechanisms for hydrocarbon oxidation at low and intermediate temperatures.

Degree: 2011, Drexel University

In the absence of scalable alternative energy sources that are greenhouse gas (GHG) neutral, hydrocarbon fuels are expected to continue to be a large part… (more)

Subjects/Keywords: Mechanical engineering; Mechanics, Analytic; Lactones

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APA (6th Edition):

Gupta, A. (2011). Development of detailed, reduced and skeletal kinetic mechanisms for hydrocarbon oxidation at low and intermediate temperatures. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/3518

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):

Gupta, Ashutosh. “Development of detailed, reduced and skeletal kinetic mechanisms for hydrocarbon oxidation at low and intermediate temperatures.” 2011. Thesis, Drexel University. Accessed December 02, 2020. http://hdl.handle.net/1860/3518.

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

MLA Handbook (7th Edition):

Gupta, Ashutosh. “Development of detailed, reduced and skeletal kinetic mechanisms for hydrocarbon oxidation at low and intermediate temperatures.” 2011. Web. 02 Dec 2020.

Vancouver:

Gupta A. Development of detailed, reduced and skeletal kinetic mechanisms for hydrocarbon oxidation at low and intermediate temperatures. [Internet] [Thesis]. Drexel University; 2011. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1860/3518.

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

Council of Science Editors:

Gupta A. Development of detailed, reduced and skeletal kinetic mechanisms for hydrocarbon oxidation at low and intermediate temperatures. [Thesis]. Drexel University; 2011. Available from: http://hdl.handle.net/1860/3518

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

7. Rammohan Reddy Teega. studies toward the synthesis of bioactive lactones and tetrahydropyrans;.

Degree: 2014, Osmania University

newline

Advisors/Committee Members: Sabitha G.

Subjects/Keywords: Lactones; Tetrahydropyrans

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APA (6th Edition):

Teega, R. R. (2014). studies toward the synthesis of bioactive lactones and tetrahydropyrans;. (Thesis). Osmania University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/20356

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):

Teega, Rammohan Reddy. “studies toward the synthesis of bioactive lactones and tetrahydropyrans;.” 2014. Thesis, Osmania University. Accessed December 02, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/20356.

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

MLA Handbook (7th Edition):

Teega, Rammohan Reddy. “studies toward the synthesis of bioactive lactones and tetrahydropyrans;.” 2014. Web. 02 Dec 2020.

Vancouver:

Teega RR. studies toward the synthesis of bioactive lactones and tetrahydropyrans;. [Internet] [Thesis]. Osmania University; 2014. [cited 2020 Dec 02]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/20356.

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

Council of Science Editors:

Teega RR. studies toward the synthesis of bioactive lactones and tetrahydropyrans;. [Thesis]. Osmania University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/20356

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

8. Shashikanth, B. Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -.

Degree: Chemistry, 2013, Jawaharlal Nehru Technological University, Hyderabad

The present study is focussed on the stereoselective total synthesis of some naturally occurring lactones, semiplenamides and isolation of bioactive natural products. newline6-Substituted-5,6-dihydro-2H-pyran-2-one is an… (more)

Subjects/Keywords: Lactones; Multifida; Semiplenamides; Synthesis

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APA (6th Edition):

Shashikanth, B. (2013). Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -. (Thesis). Jawaharlal Nehru Technological University, Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/18480

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):

Shashikanth, B. “Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -.” 2013. Thesis, Jawaharlal Nehru Technological University, Hyderabad. Accessed December 02, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/18480.

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

MLA Handbook (7th Edition):

Shashikanth, B. “Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -.” 2013. Web. 02 Dec 2020.

Vancouver:

Shashikanth B. Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. [cited 2020 Dec 02]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/18480.

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

Council of Science Editors:

Shashikanth B. Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -. [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/18480

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

9. Balasubramanyam, P. Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -.

Degree: Chemistry, 2012, Jawaharlal Nehru Technological University, Hyderabad

The thesis entitled Stereoselective Total Synthesis of Biologically Active Lactones: Synargentolide A, Cryptofolione and newlineCryptocaryalactone along with the Development of Novel Synthetic Methodologies has been… (more)

Subjects/Keywords: biologically; lactones; methodologies; Stereoselective; synthesis

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APA (6th Edition):

Balasubramanyam, P. (2012). Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -. (Thesis). Jawaharlal Nehru Technological University, Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19106

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):

Balasubramanyam, P. “Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -.” 2012. Thesis, Jawaharlal Nehru Technological University, Hyderabad. Accessed December 02, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/19106.

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

MLA Handbook (7th Edition):

Balasubramanyam, P. “Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -.” 2012. Web. 02 Dec 2020.

Vancouver:

Balasubramanyam P. Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2012. [cited 2020 Dec 02]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19106.

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

Council of Science Editors:

Balasubramanyam P. Stereoselective total synthesis of biologically active lactones: Synargentolide A, Cryptofolione and Cryptocaryalactone along with the development of novel synthetic methodologies; -. [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19106

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

10. Shashikanth B. Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -.

Degree: Chemistry, 2013, Jawaharlal Nehru Technological University, Hyderabad

The present study is focussed on the stereoselective total synthesis of some naturally occurring lactones, semiplenamides and isolation of bioactive natural products. newline6-Substituted-5,6-dihydro-2H-pyran-2-one is an… (more)

Subjects/Keywords: Jatropha; lactones; Multifida; Semiplenamides; Synthesis

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APA (6th Edition):

B, S. (2013). Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -. (Thesis). Jawaharlal Nehru Technological University, Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19245

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):

B, Shashikanth. “Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -.” 2013. Thesis, Jawaharlal Nehru Technological University, Hyderabad. Accessed December 02, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/19245.

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

MLA Handbook (7th Edition):

B, Shashikanth. “Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -.” 2013. Web. 02 Dec 2020.

Vancouver:

B S. Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. [cited 2020 Dec 02]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19245.

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

Council of Science Editors:

B S. Total Synthesis of naturally occurring lactones and Semiplenamides C and E and Investigation on Novel Diterpenoids of Jatropha Multifida; -. [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19245

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


University of Adelaide

11. Gara, Andrew Paul. The synthesis and reactions of enol-lactones : Some skeletal rearr angement processes of phosphoranes upon electron impact.

Degree: 1970, University of Adelaide

Subjects/Keywords: Lactones; Ylides

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APA (6th Edition):

Gara, A. P. (1970). The synthesis and reactions of enol-lactones : Some skeletal rearr angement processes of phosphoranes upon electron impact. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/122156

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):

Gara, Andrew Paul. “The synthesis and reactions of enol-lactones : Some skeletal rearr angement processes of phosphoranes upon electron impact.” 1970. Thesis, University of Adelaide. Accessed December 02, 2020. http://hdl.handle.net/2440/122156.

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

MLA Handbook (7th Edition):

Gara, Andrew Paul. “The synthesis and reactions of enol-lactones : Some skeletal rearr angement processes of phosphoranes upon electron impact.” 1970. Web. 02 Dec 2020.

Vancouver:

Gara AP. The synthesis and reactions of enol-lactones : Some skeletal rearr angement processes of phosphoranes upon electron impact. [Internet] [Thesis]. University of Adelaide; 1970. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/2440/122156.

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

Council of Science Editors:

Gara AP. The synthesis and reactions of enol-lactones : Some skeletal rearr angement processes of phosphoranes upon electron impact. [Thesis]. University of Adelaide; 1970. Available from: http://hdl.handle.net/2440/122156

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


Hong Kong University of Science and Technology

12. Sang, Ruocheng. Total syntheses of aogacillins A and B.

Degree: 2015, Hong Kong University of Science and Technology

 Total synthesis of natural products is a flagship and pivot of organic synthetic chemistry. Not only does it serve for structural identification and elucidation, but… (more)

Subjects/Keywords: Lactones ; Synthesis ; Natural products ; Biosynthesis

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APA (6th Edition):

Sang, R. (2015). Total syntheses of aogacillins A and B. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-79431 ; https://doi.org/10.14711/thesis-b1487652 ; http://repository.ust.hk/ir/bitstream/1783.1-79431/1/th_redirect.html

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):

Sang, Ruocheng. “Total syntheses of aogacillins A and B.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed December 02, 2020. http://repository.ust.hk/ir/Record/1783.1-79431 ; https://doi.org/10.14711/thesis-b1487652 ; http://repository.ust.hk/ir/bitstream/1783.1-79431/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Sang, Ruocheng. “Total syntheses of aogacillins A and B.” 2015. Web. 02 Dec 2020.

Vancouver:

Sang R. Total syntheses of aogacillins A and B. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2020 Dec 02]. Available from: http://repository.ust.hk/ir/Record/1783.1-79431 ; https://doi.org/10.14711/thesis-b1487652 ; http://repository.ust.hk/ir/bitstream/1783.1-79431/1/th_redirect.html.

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

Council of Science Editors:

Sang R. Total syntheses of aogacillins A and B. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: http://repository.ust.hk/ir/Record/1783.1-79431 ; https://doi.org/10.14711/thesis-b1487652 ; http://repository.ust.hk/ir/bitstream/1783.1-79431/1/th_redirect.html

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


Hong Kong University of Science and Technology

13. Wu, Yandong. Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain.

Degree: 2014, Hong Kong University of Science and Technology

 Marine microorganisms are widely viewed as an emerging source of novel natural products. A variety of butenolides [or furan-2(5H)-ones], featured with an α,β-unsaturated lactone core,… (more)

Subjects/Keywords: Organic compounds ; Synthesis ; Lactones ; Stereochemistry

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APA (6th Edition):

Wu, Y. (2014). Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-92010 ; https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/th_redirect.html

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):

Wu, Yandong. “Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed December 02, 2020. http://repository.ust.hk/ir/Record/1783.1-92010 ; https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Wu, Yandong. “Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain.” 2014. Web. 02 Dec 2020.

Vancouver:

Wu Y. Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Dec 02]. Available from: http://repository.ust.hk/ir/Record/1783.1-92010 ; https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/th_redirect.html.

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

Council of Science Editors:

Wu Y. Total synthesis of marine butenolides possessing a remote stereogenic center on the side chain. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-92010 ; https://doi.org/10.14711/thesis-b1274394 ; http://repository.ust.hk/ir/bitstream/1783.1-92010/1/th_redirect.html

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


Hong Kong University of Science and Technology

14. Ye, Ning. Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies.

Degree: 2014, Hong Kong University of Science and Technology

 Total synthesis of natural products is the Holy Grail of chemical science. Not only does it serve for structural elucidation, but also as an enabling… (more)

Subjects/Keywords: Organic compounds ; Synthesis ; Stereoisomers ; Lactones

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

APA (6th Edition):

Ye, N. (2014). Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-92011 ; https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/th_redirect.html

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):

Ye, Ning. “Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed December 02, 2020. http://repository.ust.hk/ir/Record/1783.1-92011 ; https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Ye, Ning. “Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies.” 2014. Web. 02 Dec 2020.

Vancouver:

Ye N. Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Dec 02]. Available from: http://repository.ust.hk/ir/Record/1783.1-92011 ; https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/th_redirect.html.

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

Council of Science Editors:

Ye N. Total synthesis of mycolactone E and iriomoteolide-1b stereoisomer via ring-closing metathesis strategies. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-92011 ; https://doi.org/10.14711/thesis-b1274401 ; http://repository.ust.hk/ir/bitstream/1783.1-92011/1/th_redirect.html

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


Hong Kong University of Science and Technology

15. Zhao, Wanxiang. New strategies for efficient synthesis of medium-sized lactones and lactams.

Degree: 2014, Hong Kong University of Science and Technology

 Medium-sized lactones and lactams (eight to eleven-membered rings) are important components in natural products with a diverse set of biological activities. In the last few… (more)

Subjects/Keywords: Lactones ; Synthesis ; Lactams ; Natural products

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APA (6th Edition):

Zhao, W. (2014). New strategies for efficient synthesis of medium-sized lactones and lactams. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-92013 ; https://doi.org/10.14711/thesis-b1274403 ; http://repository.ust.hk/ir/bitstream/1783.1-92013/1/th_redirect.html

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):

Zhao, Wanxiang. “New strategies for efficient synthesis of medium-sized lactones and lactams.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed December 02, 2020. http://repository.ust.hk/ir/Record/1783.1-92013 ; https://doi.org/10.14711/thesis-b1274403 ; http://repository.ust.hk/ir/bitstream/1783.1-92013/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Zhao, Wanxiang. “New strategies for efficient synthesis of medium-sized lactones and lactams.” 2014. Web. 02 Dec 2020.

Vancouver:

Zhao W. New strategies for efficient synthesis of medium-sized lactones and lactams. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2020 Dec 02]. Available from: http://repository.ust.hk/ir/Record/1783.1-92013 ; https://doi.org/10.14711/thesis-b1274403 ; http://repository.ust.hk/ir/bitstream/1783.1-92013/1/th_redirect.html.

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

Council of Science Editors:

Zhao W. New strategies for efficient synthesis of medium-sized lactones and lactams. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: http://repository.ust.hk/ir/Record/1783.1-92013 ; https://doi.org/10.14711/thesis-b1274403 ; http://repository.ust.hk/ir/bitstream/1783.1-92013/1/th_redirect.html

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


University of Hong Kong

16. 于洋. Synthetic studies towards (+)-anthecularin.

Degree: 2015, University of Hong Kong

Subjects/Keywords: Lactones - Synthesis

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

APA (6th Edition):

于洋. (2015). Synthetic studies towards (+)-anthecularin. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/226790

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

Chicago Manual of Style (16th Edition):

于洋. “Synthetic studies towards (+)-anthecularin.” 2015. Thesis, University of Hong Kong. Accessed December 02, 2020. http://hdl.handle.net/10722/226790.

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

MLA Handbook (7th Edition):

于洋. “Synthetic studies towards (+)-anthecularin.” 2015. Web. 02 Dec 2020.

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

Vancouver:

于洋. Synthetic studies towards (+)-anthecularin. [Internet] [Thesis]. University of Hong Kong; 2015. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/10722/226790.

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

Council of Science Editors:

于洋. Synthetic studies towards (+)-anthecularin. [Thesis]. University of Hong Kong; 2015. Available from: http://hdl.handle.net/10722/226790

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


Georgia Tech

17. Hasenhuettl, Gerard Leo. Approaches to the synthesis of euparotin.

Degree: PhD, Chemistry, 1977, Georgia Tech

Subjects/Keywords: Sesquiterpene lactones

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APA (6th Edition):

Hasenhuettl, G. L. (1977). Approaches to the synthesis of euparotin. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/27339

Chicago Manual of Style (16th Edition):

Hasenhuettl, Gerard Leo. “Approaches to the synthesis of euparotin.” 1977. Doctoral Dissertation, Georgia Tech. Accessed December 02, 2020. http://hdl.handle.net/1853/27339.

MLA Handbook (7th Edition):

Hasenhuettl, Gerard Leo. “Approaches to the synthesis of euparotin.” 1977. Web. 02 Dec 2020.

Vancouver:

Hasenhuettl GL. Approaches to the synthesis of euparotin. [Internet] [Doctoral dissertation]. Georgia Tech; 1977. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1853/27339.

Council of Science Editors:

Hasenhuettl GL. Approaches to the synthesis of euparotin. [Doctoral Dissertation]. Georgia Tech; 1977. Available from: http://hdl.handle.net/1853/27339


University of Limerick

18. Mullane, Nessa S. Toward the development of y-lactones and y-lactams as protease inhibitors.

Degree: 2012, University of Limerick

peer-reviewed

A select set of y-lactones, y-lactams and related bicyclic y-lactams - pyrrolothiazole[2,1b]thiazoles - were designed, synthesised and evaluated enzymatically as inhibitors of the serine… (more)

Subjects/Keywords: y-lactones; y-lactams; chemistry

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APA (6th Edition):

Mullane, N. S. (2012). Toward the development of y-lactones and y-lactams as protease inhibitors. (Thesis). University of Limerick. Retrieved from http://hdl.handle.net/10344/6258

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):

Mullane, Nessa S. “Toward the development of y-lactones and y-lactams as protease inhibitors.” 2012. Thesis, University of Limerick. Accessed December 02, 2020. http://hdl.handle.net/10344/6258.

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

MLA Handbook (7th Edition):

Mullane, Nessa S. “Toward the development of y-lactones and y-lactams as protease inhibitors.” 2012. Web. 02 Dec 2020.

Vancouver:

Mullane NS. Toward the development of y-lactones and y-lactams as protease inhibitors. [Internet] [Thesis]. University of Limerick; 2012. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/10344/6258.

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

Council of Science Editors:

Mullane NS. Toward the development of y-lactones and y-lactams as protease inhibitors. [Thesis]. University of Limerick; 2012. Available from: http://hdl.handle.net/10344/6258

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


Rutgers University

19. Zhang, Nan, 1988-. Analytical, in vitro and in vivo metabolic studies of short chain cyclic polyester oligomers (lactones) from polyurethane laminating adhesives.

Degree: MS, Food Science, 2014, Rutgers University

 Polyurethane (PU) laminating adhesive for food packaging is often formulated with polyester polyol to impart soft chain segments for the material’s flexibility. Polyester polyol synthesis… (more)

Subjects/Keywords: Food – Packaging; Polyurethanes; Adhesives; Lactones

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APA (6th Edition):

Zhang, Nan, 1. (2014). Analytical, in vitro and in vivo metabolic studies of short chain cyclic polyester oligomers (lactones) from polyurethane laminating adhesives. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/45590/

Chicago Manual of Style (16th Edition):

Zhang, Nan, 1988-. “Analytical, in vitro and in vivo metabolic studies of short chain cyclic polyester oligomers (lactones) from polyurethane laminating adhesives.” 2014. Masters Thesis, Rutgers University. Accessed December 02, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/45590/.

MLA Handbook (7th Edition):

Zhang, Nan, 1988-. “Analytical, in vitro and in vivo metabolic studies of short chain cyclic polyester oligomers (lactones) from polyurethane laminating adhesives.” 2014. Web. 02 Dec 2020.

Vancouver:

Zhang, Nan 1. Analytical, in vitro and in vivo metabolic studies of short chain cyclic polyester oligomers (lactones) from polyurethane laminating adhesives. [Internet] [Masters thesis]. Rutgers University; 2014. [cited 2020 Dec 02]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45590/.

Council of Science Editors:

Zhang, Nan 1. Analytical, in vitro and in vivo metabolic studies of short chain cyclic polyester oligomers (lactones) from polyurethane laminating adhesives. [Masters Thesis]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45590/


University of Texas – Austin

20. Davoren, Jennifer Elizabeth. Studies towards the asymmetric total synthesis of solandelactone oxylipins: the total synthesis of solandelactone E.

Degree: PhD, Chemistry, 2006, University of Texas – Austin

 A stereocontrolled approach to the elaborate skeleton of the solandelactone oxylipins culminating in the total synthesis of solandelactone E in 26 steps and 0.7% overall… (more)

Subjects/Keywords: Lactones – Synthesis

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APA (6th Edition):

Davoren, J. E. (2006). Studies towards the asymmetric total synthesis of solandelactone oxylipins: the total synthesis of solandelactone E. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/2709

Chicago Manual of Style (16th Edition):

Davoren, Jennifer Elizabeth. “Studies towards the asymmetric total synthesis of solandelactone oxylipins: the total synthesis of solandelactone E.” 2006. Doctoral Dissertation, University of Texas – Austin. Accessed December 02, 2020. http://hdl.handle.net/2152/2709.

MLA Handbook (7th Edition):

Davoren, Jennifer Elizabeth. “Studies towards the asymmetric total synthesis of solandelactone oxylipins: the total synthesis of solandelactone E.” 2006. Web. 02 Dec 2020.

Vancouver:

Davoren JE. Studies towards the asymmetric total synthesis of solandelactone oxylipins: the total synthesis of solandelactone E. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2006. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/2152/2709.

Council of Science Editors:

Davoren JE. Studies towards the asymmetric total synthesis of solandelactone oxylipins: the total synthesis of solandelactone E. [Doctoral Dissertation]. University of Texas – Austin; 2006. Available from: http://hdl.handle.net/2152/2709


Simon Fraser University

21. Lafontaine, Jean Pierre. [2+2] photocycloadditions of (alpha), (beta) -unsaturated lactones with acrylonitrile and its (alpha) -chloro and (alpha) -acetoxy derivatives.

Degree: 1987, Simon Fraser University

Subjects/Keywords: Lactones.; Photochemistry.

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APA (6th Edition):

Lafontaine, J. P. (1987). [2+2] photocycloadditions of (alpha), (beta) -unsaturated lactones with acrylonitrile and its (alpha) -chloro and (alpha) -acetoxy derivatives. (Thesis). Simon Fraser University. Retrieved from http://summit.sfu.ca/item/5312

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):

Lafontaine, Jean Pierre. “[2+2] photocycloadditions of (alpha), (beta) -unsaturated lactones with acrylonitrile and its (alpha) -chloro and (alpha) -acetoxy derivatives.” 1987. Thesis, Simon Fraser University. Accessed December 02, 2020. http://summit.sfu.ca/item/5312.

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

MLA Handbook (7th Edition):

Lafontaine, Jean Pierre. “[2+2] photocycloadditions of (alpha), (beta) -unsaturated lactones with acrylonitrile and its (alpha) -chloro and (alpha) -acetoxy derivatives.” 1987. Web. 02 Dec 2020.

Vancouver:

Lafontaine JP. [2+2] photocycloadditions of (alpha), (beta) -unsaturated lactones with acrylonitrile and its (alpha) -chloro and (alpha) -acetoxy derivatives. [Internet] [Thesis]. Simon Fraser University; 1987. [cited 2020 Dec 02]. Available from: http://summit.sfu.ca/item/5312.

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

Council of Science Editors:

Lafontaine JP. [2+2] photocycloadditions of (alpha), (beta) -unsaturated lactones with acrylonitrile and its (alpha) -chloro and (alpha) -acetoxy derivatives. [Thesis]. Simon Fraser University; 1987. Available from: http://summit.sfu.ca/item/5312

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

22. Papalos, John George. A Study of the Synthesis and Reactions of Enol Lactones.

Degree: 1959, North Texas State College

The purpose of this investigation was to study the syntheses of enol lactones and to prepare a series of amide derivatives of these compounds. Advisors/Committee Members: Truitt, Price, York, Carl T..

Subjects/Keywords: enol lactones; amide; chemistry; Lactones.

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APA (6th Edition):

Papalos, J. G. (1959). A Study of the Synthesis and Reactions of Enol Lactones. (Thesis). North Texas State College. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc108061/

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):

Papalos, John George. “A Study of the Synthesis and Reactions of Enol Lactones.” 1959. Thesis, North Texas State College. Accessed December 02, 2020. https://digital.library.unt.edu/ark:/67531/metadc108061/.

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

MLA Handbook (7th Edition):

Papalos, John George. “A Study of the Synthesis and Reactions of Enol Lactones.” 1959. Web. 02 Dec 2020.

Vancouver:

Papalos JG. A Study of the Synthesis and Reactions of Enol Lactones. [Internet] [Thesis]. North Texas State College; 1959. [cited 2020 Dec 02]. Available from: https://digital.library.unt.edu/ark:/67531/metadc108061/.

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

Council of Science Editors:

Papalos JG. A Study of the Synthesis and Reactions of Enol Lactones. [Thesis]. North Texas State College; 1959. Available from: https://digital.library.unt.edu/ark:/67531/metadc108061/

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


Oregon State University

23. Hotchko, Rachel Ann. The potential role of aliphatic gamma- and delta-lactones in beer fruit aroma.

Degree: MS, Food Science and Technology, 2014, Oregon State University

 This work set out to examine the potential contribution of five aliphatic lactones, γ-nonalactone, γ-decalactone, γ-dodecalactone, δ-decalactone and δ-dodecalactone to stone fruit aroma in beer.… (more)

Subjects/Keywords: aliphatic lactones; Beer  – Flavor and odor

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APA (6th Edition):

Hotchko, R. A. (2014). The potential role of aliphatic gamma- and delta-lactones in beer fruit aroma. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/54913

Chicago Manual of Style (16th Edition):

Hotchko, Rachel Ann. “The potential role of aliphatic gamma- and delta-lactones in beer fruit aroma.” 2014. Masters Thesis, Oregon State University. Accessed December 02, 2020. http://hdl.handle.net/1957/54913.

MLA Handbook (7th Edition):

Hotchko, Rachel Ann. “The potential role of aliphatic gamma- and delta-lactones in beer fruit aroma.” 2014. Web. 02 Dec 2020.

Vancouver:

Hotchko RA. The potential role of aliphatic gamma- and delta-lactones in beer fruit aroma. [Internet] [Masters thesis]. Oregon State University; 2014. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1957/54913.

Council of Science Editors:

Hotchko RA. The potential role of aliphatic gamma- and delta-lactones in beer fruit aroma. [Masters Thesis]. Oregon State University; 2014. Available from: http://hdl.handle.net/1957/54913


University of Manchester

24. Shangula, Suha. Effect of paraoxonase (PON1) on lactones and ROS induced DNA damage.

Degree: PhD, 2018, University of Manchester

 Paraoxonase 1 (PON1) is an enzyme synthesised in the liver that is associated with High Density Lipoprotein (HDL) and increasingly with a number of human… (more)

Subjects/Keywords: 572; PON1; Lactones; Alpha angelica lactone; ROS

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APA (6th Edition):

Shangula, S. (2018). Effect of paraoxonase (PON1) on lactones and ROS induced DNA damage. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/effect-of-paraoxonase-pon1-on-lactones-and-ros-induced-dna-damage(928ac761-7039-4f6f-9135-40a6f71b9465).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748043

Chicago Manual of Style (16th Edition):

Shangula, Suha. “Effect of paraoxonase (PON1) on lactones and ROS induced DNA damage.” 2018. Doctoral Dissertation, University of Manchester. Accessed December 02, 2020. https://www.research.manchester.ac.uk/portal/en/theses/effect-of-paraoxonase-pon1-on-lactones-and-ros-induced-dna-damage(928ac761-7039-4f6f-9135-40a6f71b9465).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748043.

MLA Handbook (7th Edition):

Shangula, Suha. “Effect of paraoxonase (PON1) on lactones and ROS induced DNA damage.” 2018. Web. 02 Dec 2020.

Vancouver:

Shangula S. Effect of paraoxonase (PON1) on lactones and ROS induced DNA damage. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Dec 02]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/effect-of-paraoxonase-pon1-on-lactones-and-ros-induced-dna-damage(928ac761-7039-4f6f-9135-40a6f71b9465).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748043.

Council of Science Editors:

Shangula S. Effect of paraoxonase (PON1) on lactones and ROS induced DNA damage. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/effect-of-paraoxonase-pon1-on-lactones-and-ros-induced-dna-damage(928ac761-7039-4f6f-9135-40a6f71b9465).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748043


Hong Kong University of Science and Technology

25. Cao, Shuyong. Characterization of macrolactonization catalyzed by the excised thioesterase domain of biosurfactant lichenysin D synthetase.

Degree: 2005, Hong Kong University of Science and Technology

 Most natural cyclic peptides of pharmacological and biological importance are assembled by modular organized non-ribosomal peptide synthetases (NRPSs) in microorganisms. The carboxy terminal thioesterase (TE)… (more)

Subjects/Keywords: Lactones ; Peptides  – Synthesis

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APA (6th Edition):

Cao, S. (2005). Characterization of macrolactonization catalyzed by the excised thioesterase domain of biosurfactant lichenysin D synthetase. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-4035 ; https://doi.org/10.14711/thesis-b863991 ; http://repository.ust.hk/ir/bitstream/1783.1-4035/1/th_redirect.html

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):

Cao, Shuyong. “Characterization of macrolactonization catalyzed by the excised thioesterase domain of biosurfactant lichenysin D synthetase.” 2005. Thesis, Hong Kong University of Science and Technology. Accessed December 02, 2020. http://repository.ust.hk/ir/Record/1783.1-4035 ; https://doi.org/10.14711/thesis-b863991 ; http://repository.ust.hk/ir/bitstream/1783.1-4035/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Cao, Shuyong. “Characterization of macrolactonization catalyzed by the excised thioesterase domain of biosurfactant lichenysin D synthetase.” 2005. Web. 02 Dec 2020.

Vancouver:

Cao S. Characterization of macrolactonization catalyzed by the excised thioesterase domain of biosurfactant lichenysin D synthetase. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2005. [cited 2020 Dec 02]. Available from: http://repository.ust.hk/ir/Record/1783.1-4035 ; https://doi.org/10.14711/thesis-b863991 ; http://repository.ust.hk/ir/bitstream/1783.1-4035/1/th_redirect.html.

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

Council of Science Editors:

Cao S. Characterization of macrolactonization catalyzed by the excised thioesterase domain of biosurfactant lichenysin D synthetase. [Thesis]. Hong Kong University of Science and Technology; 2005. Available from: http://repository.ust.hk/ir/Record/1783.1-4035 ; https://doi.org/10.14711/thesis-b863991 ; http://repository.ust.hk/ir/bitstream/1783.1-4035/1/th_redirect.html

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


University of Arizona

26. Bassi, Mitchell Brian, 1963-. The mechanism of the ring-opening polymerization of ε-caprolactone using tin(IV) carboxylates .

Degree: 1987, University of Arizona

 The polymerization of epsilon-caprolactone using tin(IV) carboxylates has been investigated and related to literature research. Polymers with broad MWD were obtained in quantitative yield. At… (more)

Subjects/Keywords: Polymerization.; Lactones.; Polymers.

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APA (6th Edition):

Bassi, Mitchell Brian, 1. (1987). The mechanism of the ring-opening polymerization of ε-caprolactone using tin(IV) carboxylates . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/291748

Chicago Manual of Style (16th Edition):

Bassi, Mitchell Brian, 1963-. “The mechanism of the ring-opening polymerization of ε-caprolactone using tin(IV) carboxylates .” 1987. Masters Thesis, University of Arizona. Accessed December 02, 2020. http://hdl.handle.net/10150/291748.

MLA Handbook (7th Edition):

Bassi, Mitchell Brian, 1963-. “The mechanism of the ring-opening polymerization of ε-caprolactone using tin(IV) carboxylates .” 1987. Web. 02 Dec 2020.

Vancouver:

Bassi, Mitchell Brian 1. The mechanism of the ring-opening polymerization of ε-caprolactone using tin(IV) carboxylates . [Internet] [Masters thesis]. University of Arizona; 1987. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/10150/291748.

Council of Science Editors:

Bassi, Mitchell Brian 1. The mechanism of the ring-opening polymerization of ε-caprolactone using tin(IV) carboxylates . [Masters Thesis]. University of Arizona; 1987. Available from: http://hdl.handle.net/10150/291748


Eastern Illinois University

27. Huang, Jianhua. Butenolide Synthesis via Cation-Initiated Ring Expansion/Elimination of β-Lactones.

Degree: MS, 1992, Eastern Illinois University

  An area of recent research in the Black research group is an exploration of the potential of cation-initiated β-lactone ring expansions, accompanied by the… (more)

Subjects/Keywords: beta-lactones; Chemistry

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APA (6th Edition):

Huang, J. (1992). Butenolide Synthesis via Cation-Initiated Ring Expansion/Elimination of β-Lactones. (Masters Thesis). Eastern Illinois University. Retrieved from https://thekeep.eiu.edu/theses/1970

Chicago Manual of Style (16th Edition):

Huang, Jianhua. “Butenolide Synthesis via Cation-Initiated Ring Expansion/Elimination of β-Lactones.” 1992. Masters Thesis, Eastern Illinois University. Accessed December 02, 2020. https://thekeep.eiu.edu/theses/1970.

MLA Handbook (7th Edition):

Huang, Jianhua. “Butenolide Synthesis via Cation-Initiated Ring Expansion/Elimination of β-Lactones.” 1992. Web. 02 Dec 2020.

Vancouver:

Huang J. Butenolide Synthesis via Cation-Initiated Ring Expansion/Elimination of β-Lactones. [Internet] [Masters thesis]. Eastern Illinois University; 1992. [cited 2020 Dec 02]. Available from: https://thekeep.eiu.edu/theses/1970.

Council of Science Editors:

Huang J. Butenolide Synthesis via Cation-Initiated Ring Expansion/Elimination of β-Lactones. [Masters Thesis]. Eastern Illinois University; 1992. Available from: https://thekeep.eiu.edu/theses/1970


Eastern Illinois University

28. Yates, Bryan E. Studies Directed Toward the Synthesis of Germacranolides via [2+2] Cycloaddition Followed by Ring Expansion/Elimination of β-Lactones.

Degree: MS, 1994, Eastern Illinois University

  Exposure of α-trimethylsilyl β-lactones to magnesium bromide or boron trifluoride etherate in diethyl ether solvent resulted in the smooth generation of β,γ-unsaturated acid derivatives… (more)

Subjects/Keywords: beta-lactones; Chemistry

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APA (6th Edition):

Yates, B. E. (1994). Studies Directed Toward the Synthesis of Germacranolides via [2+2] Cycloaddition Followed by Ring Expansion/Elimination of β-Lactones. (Masters Thesis). Eastern Illinois University. Retrieved from https://thekeep.eiu.edu/theses/2029

Chicago Manual of Style (16th Edition):

Yates, Bryan E. “Studies Directed Toward the Synthesis of Germacranolides via [2+2] Cycloaddition Followed by Ring Expansion/Elimination of β-Lactones.” 1994. Masters Thesis, Eastern Illinois University. Accessed December 02, 2020. https://thekeep.eiu.edu/theses/2029.

MLA Handbook (7th Edition):

Yates, Bryan E. “Studies Directed Toward the Synthesis of Germacranolides via [2+2] Cycloaddition Followed by Ring Expansion/Elimination of β-Lactones.” 1994. Web. 02 Dec 2020.

Vancouver:

Yates BE. Studies Directed Toward the Synthesis of Germacranolides via [2+2] Cycloaddition Followed by Ring Expansion/Elimination of β-Lactones. [Internet] [Masters thesis]. Eastern Illinois University; 1994. [cited 2020 Dec 02]. Available from: https://thekeep.eiu.edu/theses/2029.

Council of Science Editors:

Yates BE. Studies Directed Toward the Synthesis of Germacranolides via [2+2] Cycloaddition Followed by Ring Expansion/Elimination of β-Lactones. [Masters Thesis]. Eastern Illinois University; 1994. Available from: https://thekeep.eiu.edu/theses/2029


Eastern Illinois University

29. Maluleka, Stephen Lucas. A Novel Synthesis of Cyclic and Acyclic 3-Alkenoic Acids via Ionization/Elimination of β-Lactones.

Degree: MS, 1989, Eastern Illinois University

  Exposure of spiro β-lactones and 3-substituted 4,4-dialkyl oxetan-2-ones to magnesium bromide in diethyl ether solvent resulted in the smooth generation of β,γ-unsaturated acid derivatives… (more)

Subjects/Keywords: beta-lactones; Chemistry

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APA (6th Edition):

Maluleka, S. L. (1989). A Novel Synthesis of Cyclic and Acyclic 3-Alkenoic Acids via Ionization/Elimination of β-Lactones. (Masters Thesis). Eastern Illinois University. Retrieved from https://thekeep.eiu.edu/theses/2346

Chicago Manual of Style (16th Edition):

Maluleka, Stephen Lucas. “A Novel Synthesis of Cyclic and Acyclic 3-Alkenoic Acids via Ionization/Elimination of β-Lactones.” 1989. Masters Thesis, Eastern Illinois University. Accessed December 02, 2020. https://thekeep.eiu.edu/theses/2346.

MLA Handbook (7th Edition):

Maluleka, Stephen Lucas. “A Novel Synthesis of Cyclic and Acyclic 3-Alkenoic Acids via Ionization/Elimination of β-Lactones.” 1989. Web. 02 Dec 2020.

Vancouver:

Maluleka SL. A Novel Synthesis of Cyclic and Acyclic 3-Alkenoic Acids via Ionization/Elimination of β-Lactones. [Internet] [Masters thesis]. Eastern Illinois University; 1989. [cited 2020 Dec 02]. Available from: https://thekeep.eiu.edu/theses/2346.

Council of Science Editors:

Maluleka SL. A Novel Synthesis of Cyclic and Acyclic 3-Alkenoic Acids via Ionization/Elimination of β-Lactones. [Masters Thesis]. Eastern Illinois University; 1989. Available from: https://thekeep.eiu.edu/theses/2346


University of Cambridge

30. Hulme, A. N. The total synthesis of (-)-ebalactone A & B.

Degree: PhD, 1993, University of Cambridge

Subjects/Keywords: 547; Beta-lactones

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APA (6th Edition):

Hulme, A. N. (1993). The total synthesis of (-)-ebalactone A & B. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.19382 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.281963

Chicago Manual of Style (16th Edition):

Hulme, A N. “The total synthesis of (-)-ebalactone A & B.” 1993. Doctoral Dissertation, University of Cambridge. Accessed December 02, 2020. https://doi.org/10.17863/CAM.19382 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.281963.

MLA Handbook (7th Edition):

Hulme, A N. “The total synthesis of (-)-ebalactone A & B.” 1993. Web. 02 Dec 2020.

Vancouver:

Hulme AN. The total synthesis of (-)-ebalactone A & B. [Internet] [Doctoral dissertation]. University of Cambridge; 1993. [cited 2020 Dec 02]. Available from: https://doi.org/10.17863/CAM.19382 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.281963.

Council of Science Editors:

Hulme AN. The total synthesis of (-)-ebalactone A & B. [Doctoral Dissertation]. University of Cambridge; 1993. Available from: https://doi.org/10.17863/CAM.19382 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.281963

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