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You searched for +publisher:"University of Illinois – Urbana-Champaign" +contributor:("Sarlah, David"). Showing records 1 – 8 of 8 total matches.

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University of Illinois – Urbana-Champaign

1. Holycross, Daniel Robert. Total synthesis of lycoricidine via photochemical dearomative dihydroxylation.

Degree: MS, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Lycoricidine a member of the amaryllidaceae isocarbostyril alkaloid family of natural products isolated from bulbs of plants in the amaryllidaceae family, which include the common… (more)

Subjects/Keywords: Lycoricidine; total synthesis; dearomative dihydroxylation

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APA (6th Edition):

Holycross, D. R. (2016). Total synthesis of lycoricidine via photochemical dearomative dihydroxylation. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95520

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):

Holycross, Daniel Robert. “Total synthesis of lycoricidine via photochemical dearomative dihydroxylation.” 2016. Thesis, University of Illinois – Urbana-Champaign. Accessed August 21, 2019. http://hdl.handle.net/2142/95520.

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

MLA Handbook (7th Edition):

Holycross, Daniel Robert. “Total synthesis of lycoricidine via photochemical dearomative dihydroxylation.” 2016. Web. 21 Aug 2019.

Vancouver:

Holycross DR. Total synthesis of lycoricidine via photochemical dearomative dihydroxylation. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 21]. Available from: http://hdl.handle.net/2142/95520.

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

Council of Science Editors:

Holycross DR. Total synthesis of lycoricidine via photochemical dearomative dihydroxylation. [Thesis]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95520

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


University of Illinois – Urbana-Champaign

2. Nakamata Huynh, Stephanie Mio. Dearomative reduction of arenes through the use of arenophiles & studies towards the synthesis of cardiotonic steroids calotropin and calactin.

Degree: MS, Chemistry, 2017, University of Illinois – Urbana-Champaign

 A novel method for the dearomative reduction of arenes through the use of N,N-arenophile, MTAD, was developed. Cheap feedstock arenes undergo photocycloaddition with MTAD, and… (more)

Subjects/Keywords: Organic chemistry; Total synthesis; Methodology; Dearomative functionalization

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APA (6th Edition):

Nakamata Huynh, S. M. (2017). Dearomative reduction of arenes through the use of arenophiles & studies towards the synthesis of cardiotonic steroids calotropin and calactin. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/97622

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):

Nakamata Huynh, Stephanie Mio. “Dearomative reduction of arenes through the use of arenophiles & studies towards the synthesis of cardiotonic steroids calotropin and calactin.” 2017. Thesis, University of Illinois – Urbana-Champaign. Accessed August 21, 2019. http://hdl.handle.net/2142/97622.

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

MLA Handbook (7th Edition):

Nakamata Huynh, Stephanie Mio. “Dearomative reduction of arenes through the use of arenophiles & studies towards the synthesis of cardiotonic steroids calotropin and calactin.” 2017. Web. 21 Aug 2019.

Vancouver:

Nakamata Huynh SM. Dearomative reduction of arenes through the use of arenophiles & studies towards the synthesis of cardiotonic steroids calotropin and calactin. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2017. [cited 2019 Aug 21]. Available from: http://hdl.handle.net/2142/97622.

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

Council of Science Editors:

Nakamata Huynh SM. Dearomative reduction of arenes through the use of arenophiles & studies towards the synthesis of cardiotonic steroids calotropin and calactin. [Thesis]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/97622

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


University of Illinois – Urbana-Champaign

3. Levinn, Carolyn M. Progress towards the enantioselective total synthesis of trichodermamide B.

Degree: MS, Chemistry, 2017, University of Illinois – Urbana-Champaign

 Trichodermamide B is an unusual modified dipeptide natural product, with very promising anticancer activities. While the biosynthesis of this molecule is unknown, it is proposed… (more)

Subjects/Keywords: Trichodermamide B; Total synthesis; Microbial arene oxidation; Arenophile; Arene oxide

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APA (6th Edition):

Levinn, C. M. (2017). Progress towards the enantioselective total synthesis of trichodermamide B. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/97625

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):

Levinn, Carolyn M. “Progress towards the enantioselective total synthesis of trichodermamide B.” 2017. Thesis, University of Illinois – Urbana-Champaign. Accessed August 21, 2019. http://hdl.handle.net/2142/97625.

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

MLA Handbook (7th Edition):

Levinn, Carolyn M. “Progress towards the enantioselective total synthesis of trichodermamide B.” 2017. Web. 21 Aug 2019.

Vancouver:

Levinn CM. Progress towards the enantioselective total synthesis of trichodermamide B. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2017. [cited 2019 Aug 21]. Available from: http://hdl.handle.net/2142/97625.

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

Council of Science Editors:

Levinn CM. Progress towards the enantioselective total synthesis of trichodermamide B. [Thesis]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/97625

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


University of Illinois – Urbana-Champaign

4. Ambrosi, Andrea. I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis.

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 The first half of the present dissertation describes the mechanistic investigation of the palladium-catalyzed cross-coupling reaction of alkenyl- and arylsilanolates. The combination of reaction kinetics… (more)

Subjects/Keywords: Cross-coupling; Silanolates; Carbon monoxide; Organic synthesis

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APA (6th Edition):

Ambrosi, A. (2016). I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95551

Chicago Manual of Style (16th Edition):

Ambrosi, Andrea. “I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 21, 2019. http://hdl.handle.net/2142/95551.

MLA Handbook (7th Edition):

Ambrosi, Andrea. “I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis.” 2016. Web. 21 Aug 2019.

Vancouver:

Ambrosi A. I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 21]. Available from: http://hdl.handle.net/2142/95551.

Council of Science Editors:

Ambrosi A. I. Mechanistic significance of the Si-O-Pd linkage in the cross-coupling of organosilanolates; II. Applications of the water-gas shift reaction in organic synthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95551


University of Illinois – Urbana-Champaign

5. Lambrecht, Michael. The chemical and enzymatic synthesis of poly(ADP-ribose).

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Poly(ADP-ribose) synthesis and degradation are important cellular processes associated with the DNA damage response and many other pathways. Traditionally, these processes have been challenging to… (more)

Subjects/Keywords: Poly(ADP-ribose); Total Synthesis; Enzymatic Synthesis; Poly(ADP-ribose) Polymerase; Poly ADP ribose polymerase (PARP); Poly(ADP-ribose) Glycohydrolase (PARG); Raptinal

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APA (6th Edition):

Lambrecht, M. (2016). The chemical and enzymatic synthesis of poly(ADP-ribose). (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/92923

Chicago Manual of Style (16th Edition):

Lambrecht, Michael. “The chemical and enzymatic synthesis of poly(ADP-ribose).” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 21, 2019. http://hdl.handle.net/2142/92923.

MLA Handbook (7th Edition):

Lambrecht, Michael. “The chemical and enzymatic synthesis of poly(ADP-ribose).” 2016. Web. 21 Aug 2019.

Vancouver:

Lambrecht M. The chemical and enzymatic synthesis of poly(ADP-ribose). [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Aug 21]. Available from: http://hdl.handle.net/2142/92923.

Council of Science Editors:

Lambrecht M. The chemical and enzymatic synthesis of poly(ADP-ribose). [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/92923


University of Illinois – Urbana-Champaign

6. Thomas, Andy Alexander. Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link.

Degree: PhD, Chemistry, 2017, University of Illinois – Urbana-Champaign

 The Suzuki-Miyaura reaction is currently the most practiced cross-coupling reaction due to its broad applicability, low toxicity of the metal (B), and the wide variety… (more)

Subjects/Keywords: Transmetalation

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APA (6th Edition):

Thomas, A. A. (2017). Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/97541

Chicago Manual of Style (16th Edition):

Thomas, Andy Alexander. “Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 21, 2019. http://hdl.handle.net/2142/97541.

MLA Handbook (7th Edition):

Thomas, Andy Alexander. “Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link.” 2017. Web. 21 Aug 2019.

Vancouver:

Thomas AA. Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2019 Aug 21]. Available from: http://hdl.handle.net/2142/97541.

Council of Science Editors:

Thomas AA. Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: the missing link. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/97541

7. Reynolds, Bryan Joseph. Synthetic studies towards trichodermamide B: expedient synthesis enabled by arene oxide equivalents.

Degree: MS, Chemistry, 2015, University of Illinois – Urbana-Champaign

 Trichodermamide B, isolated from the marine fungus Trichoderma virens in 2003, is a potent anti-cancer agent and with complex molecular architecture. It is hypothesized herein… (more)

Subjects/Keywords: Trichodermamide B; arene oxide; dearomatization; alkylation; natural product; total synthesis; biomimetic

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APA (6th Edition):

Reynolds, B. J. (2015). Synthetic studies towards trichodermamide B: expedient synthesis enabled by arene oxide equivalents. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89043

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):

Reynolds, Bryan Joseph. “Synthetic studies towards trichodermamide B: expedient synthesis enabled by arene oxide equivalents.” 2015. Thesis, University of Illinois – Urbana-Champaign. Accessed August 21, 2019. http://hdl.handle.net/2142/89043.

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

MLA Handbook (7th Edition):

Reynolds, Bryan Joseph. “Synthetic studies towards trichodermamide B: expedient synthesis enabled by arene oxide equivalents.” 2015. Web. 21 Aug 2019.

Vancouver:

Reynolds BJ. Synthetic studies towards trichodermamide B: expedient synthesis enabled by arene oxide equivalents. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Aug 21]. Available from: http://hdl.handle.net/2142/89043.

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

Council of Science Editors:

Reynolds BJ. Synthetic studies towards trichodermamide B: expedient synthesis enabled by arene oxide equivalents. [Thesis]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89043

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

8. Wang, Puzhou. DNA enzymes for tyrosine PEGylation and azido-adenylylation of peptide and protein substrates.

Degree: PhD, Chemistry, 2018, University of Illinois – Urbana-Champaign

 Proteins and RNA are used as enzymes in nature, while DNA is used for the storage and transfer of genetic information. Proteins and RNA are… (more)

Subjects/Keywords: DNA enzyme; deoxyribozyme; peptide; protein; PEGylation; azido-adenylylation

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APA (6th Edition):

Wang, P. (2018). DNA enzymes for tyrosine PEGylation and azido-adenylylation of peptide and protein substrates. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/101524

Chicago Manual of Style (16th Edition):

Wang, Puzhou. “DNA enzymes for tyrosine PEGylation and azido-adenylylation of peptide and protein substrates.” 2018. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 21, 2019. http://hdl.handle.net/2142/101524.

MLA Handbook (7th Edition):

Wang, Puzhou. “DNA enzymes for tyrosine PEGylation and azido-adenylylation of peptide and protein substrates.” 2018. Web. 21 Aug 2019.

Vancouver:

Wang P. DNA enzymes for tyrosine PEGylation and azido-adenylylation of peptide and protein substrates. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2018. [cited 2019 Aug 21]. Available from: http://hdl.handle.net/2142/101524.

Council of Science Editors:

Wang P. DNA enzymes for tyrosine PEGylation and azido-adenylylation of peptide and protein substrates. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2018. Available from: http://hdl.handle.net/2142/101524

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