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You searched for +publisher:"Rutgers University" +contributor:("Jimenez, Leslie "). Showing records 1 – 7 of 7 total matches.

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Rutgers University

1. Chie, Yu-Ming, 1980-. Synthesis of new phosphorus ligands for regioselective hydroformylation:.

Degree: MS, Chemistry, 2010, Rutgers University

 Tetraphosphorous ligands with enhanced chelating ability through multiple chelating modes and increased local phosphorus concentration can provide great regioselectivity in Rh/Ligand hydroformylation system. Here we… (more)

Subjects/Keywords: Ligands – Synthesis; Hydroformylation

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APA (6th Edition):

Chie, Yu-Ming, 1. (2010). Synthesis of new phosphorus ligands for regioselective hydroformylation:. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052101

Chicago Manual of Style (16th Edition):

Chie, Yu-Ming, 1980-. “Synthesis of new phosphorus ligands for regioselective hydroformylation:.” 2010. Masters Thesis, Rutgers University. Accessed March 25, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052101.

MLA Handbook (7th Edition):

Chie, Yu-Ming, 1980-. “Synthesis of new phosphorus ligands for regioselective hydroformylation:.” 2010. Web. 25 Mar 2019.

Vancouver:

Chie, Yu-Ming 1. Synthesis of new phosphorus ligands for regioselective hydroformylation:. [Internet] [Masters thesis]. Rutgers University; 2010. [cited 2019 Mar 25]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052101.

Council of Science Editors:

Chie, Yu-Ming 1. Synthesis of new phosphorus ligands for regioselective hydroformylation:. [Masters Thesis]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000052101


Rutgers University

2. Demirdirek, Bahar. Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications.

Degree: MS, Chemistry and Chemical Biology, 2009, Rutgers University

 Self-assembled and unimolecular amphiphilic macromolecules with pseudo-double branched and single tails were synthesized. Degradation behavior, drug loading efficiency, drug release rate and stability of macromolecules… (more)

Subjects/Keywords: Drug delivery systems

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APA (6th Edition):

Demirdirek, B. (2009). Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505

Chicago Manual of Style (16th Edition):

Demirdirek, Bahar. “Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications.” 2009. Masters Thesis, Rutgers University. Accessed March 25, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505.

MLA Handbook (7th Edition):

Demirdirek, Bahar. “Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications.” 2009. Web. 25 Mar 2019.

Vancouver:

Demirdirek B. Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications. [Internet] [Masters thesis]. Rutgers University; 2009. [cited 2019 Mar 25]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505.

Council of Science Editors:

Demirdirek B. Synthesis and evaluation of amphiphilic scorpion-like and star macromolecules for biomedical applications. [Masters Thesis]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000050505


Rutgers University

3. Carbone, Ashley Lauren, 1984. Natural bioactive-based polyanhydrides for controlled release applications:.

Degree: PhD, Chemistry, 2009, Rutgers University

Hydrolytically degradable polyanhydrides are of interest for a variety of controlled release applications because of their surface-eroding behavior and tunable degradation rate based on polymer… (more)

Subjects/Keywords: Controlled release technology; Anhydrides

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APA (6th Edition):

Carbone, Ashley Lauren, 1. (2009). Natural bioactive-based polyanhydrides for controlled release applications:. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051788

Chicago Manual of Style (16th Edition):

Carbone, Ashley Lauren, 1984. “Natural bioactive-based polyanhydrides for controlled release applications:.” 2009. Doctoral Dissertation, Rutgers University. Accessed March 25, 2019. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051788.

MLA Handbook (7th Edition):

Carbone, Ashley Lauren, 1984. “Natural bioactive-based polyanhydrides for controlled release applications:.” 2009. Web. 25 Mar 2019.

Vancouver:

Carbone, Ashley Lauren 1. Natural bioactive-based polyanhydrides for controlled release applications:. [Internet] [Doctoral dissertation]. Rutgers University; 2009. [cited 2019 Mar 25]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051788.

Council of Science Editors:

Carbone, Ashley Lauren 1. Natural bioactive-based polyanhydrides for controlled release applications:. [Doctoral Dissertation]. Rutgers University; 2009. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000051788


Rutgers University

4. Ramanathan, Ahalya. I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily.

Degree: PhD, Chemistry and Chemical Biology, 2011, Rutgers University

TMC-95A is a natural product which has demonstrated inhibition activity against the proteasomal pathway. Though its biological activity is proven, the total synthesis of the… (more)

Subjects/Keywords: Chemistry, Organic; Organic compounds – Synthesis

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APA (6th Edition):

Ramanathan, A. (2011). I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673

Chicago Manual of Style (16th Edition):

Ramanathan, Ahalya. “I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily.” 2011. Doctoral Dissertation, Rutgers University. Accessed March 25, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673.

MLA Handbook (7th Edition):

Ramanathan, Ahalya. “I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily.” 2011. Web. 25 Mar 2019.

Vancouver:

Ramanathan A. I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2019 Mar 25]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673.

Council of Science Editors:

Ramanathan A. I. New strategy for the synthesis of TMC-95A II. Selective ortho-substitution on substituted aryl rings III. Characterization of steroidal glycosides from easter lily. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000057673

5. Mootoosammy, Davena. Synthesis of the 16-membered BCD ring of complestatin and halogenation of the tryptophan indole.

Degree: MS, Chemistry and Chemical Biology, 2011, Rutgers University

 Complestatin is a natural product that has demonstrated inhibition activity against HIV-1 integrase and initiation of the complement pathway. Though its biological activity is proven,… (more)

Subjects/Keywords: HIV infections – Treatment; Microbiological synthesis

…Spectrometry facility or Finnigan LCQ-DUO mass spectrometer from Chemistry Department, Rutgers… …University, New Brunswick, NJ. Materials. Unless otherwise specified, all materials were purchased… 

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APA (6th Edition):

Mootoosammy, D. (2011). Synthesis of the 16-membered BCD ring of complestatin and halogenation of the tryptophan indole. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061362

Chicago Manual of Style (16th Edition):

Mootoosammy, Davena. “Synthesis of the 16-membered BCD ring of complestatin and halogenation of the tryptophan indole.” 2011. Masters Thesis, Rutgers University. Accessed March 25, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061362.

MLA Handbook (7th Edition):

Mootoosammy, Davena. “Synthesis of the 16-membered BCD ring of complestatin and halogenation of the tryptophan indole.” 2011. Web. 25 Mar 2019.

Vancouver:

Mootoosammy D. Synthesis of the 16-membered BCD ring of complestatin and halogenation of the tryptophan indole. [Internet] [Masters thesis]. Rutgers University; 2011. [cited 2019 Mar 25]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061362.

Council of Science Editors:

Mootoosammy D. Synthesis of the 16-membered BCD ring of complestatin and halogenation of the tryptophan indole. [Masters Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061362

6. Zhang, Sisi, 1987-. Gas phase reactivity studies of organic species using mass spectrometry.

Degree: MS, Chemistry and Chemical Biology, 2012, Rutgers University

 DNA damaged bases are one of the reasons for a variety diseases, such as carcinogenesis, aging and cell death. uracil is a nucleobase that arises… (more)

Subjects/Keywords: Mass spectrometry; Protons – Affinity labeling; Acidity function

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

APA (6th Edition):

Zhang, Sisi, 1. (2012). Gas phase reactivity studies of organic species using mass spectrometry. (Masters Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067039

Chicago Manual of Style (16th Edition):

Zhang, Sisi, 1987-. “Gas phase reactivity studies of organic species using mass spectrometry.” 2012. Masters Thesis, Rutgers University. Accessed March 25, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067039.

MLA Handbook (7th Edition):

Zhang, Sisi, 1987-. “Gas phase reactivity studies of organic species using mass spectrometry.” 2012. Web. 25 Mar 2019.

Vancouver:

Zhang, Sisi 1. Gas phase reactivity studies of organic species using mass spectrometry. [Internet] [Masters thesis]. Rutgers University; 2012. [cited 2019 Mar 25]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067039.

Council of Science Editors:

Zhang, Sisi 1. Gas phase reactivity studies of organic species using mass spectrometry. [Masters Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000067039

7. Pan, Weidong, 1966-. Total synthesis of 7-Epi-FR 66979 and 7-Epi-FR 900482.

Degree: PhD, Chemistry and Chemical Biology, 2010, Rutgers University

The completion of the total synthesis of 7-Epi-FR 66979 and 7-Epi-FR 900482 is presented in this thesis. The natural product FR 66979 and FR 900482… (more)

Subjects/Keywords: Streptomyces – Synthesis; Antibiotics – Synthesis

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APA (6th Edition):

Pan, Weidong, 1. (2010). Total synthesis of 7-Epi-FR 66979 and 7-Epi-FR 900482. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000053410

Chicago Manual of Style (16th Edition):

Pan, Weidong, 1966-. “Total synthesis of 7-Epi-FR 66979 and 7-Epi-FR 900482.” 2010. Doctoral Dissertation, Rutgers University. Accessed March 25, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000053410.

MLA Handbook (7th Edition):

Pan, Weidong, 1966-. “Total synthesis of 7-Epi-FR 66979 and 7-Epi-FR 900482.” 2010. Web. 25 Mar 2019.

Vancouver:

Pan, Weidong 1. Total synthesis of 7-Epi-FR 66979 and 7-Epi-FR 900482. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Mar 25]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000053410.

Council of Science Editors:

Pan, Weidong 1. Total synthesis of 7-Epi-FR 66979 and 7-Epi-FR 900482. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000053410

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