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Nickel Catalyzed Regioselective Reductive Coupling Reactions

Rodrigo, Sanjeewa K
http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622

Abstract Details

2014, PhD, University of Cincinnati, Arts and Sciences: Chemistry.
Coupling or cycloaddition of two different p-components for the construction of more complex structural motifs is commonly used in organic synthesis. Most of these systems involve a transition metal based catalyst and for reductive coupling reactions, various reducing agents are also employed. This dissertation is focused on the development and mechanistic investigation of nickel-catalyzed reductive coupling processes for useful organic transformations, specifically the coupling of aldehydes and alkynes and the cyclotrimerization of alkynes.
Hairong Guan, Ph.D. (Committee Chair)
William Connick, Ph.D. (Committee Member)
James Mack, Ph.D. (Committee Member)
Allan Pinhas, Ph.D. (Committee Member)
227 p.
Analytical Chemistry; Chemistry
reductive coupling reactions; cycloaddition

Recommended Citations

Citations

  • Rodrigo, S. K. (2014). Nickel Catalyzed Regioselective Reductive Coupling Reactions [Doctoral dissertation, University of Cincinnati]. OhioLINK Electronic Theses and Dissertations Center. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622

    APA Style (7th edition)

  • Rodrigo, Sanjeewa. Nickel Catalyzed Regioselective Reductive Coupling Reactions. 2014. University of Cincinnati, Doctoral dissertation. OhioLINK Electronic Theses and Dissertations Center, http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622.

    MLA Style (8th edition)

  • Rodrigo, Sanjeewa. "Nickel Catalyzed Regioselective Reductive Coupling Reactions." Doctoral dissertation, University of Cincinnati, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622

    Chicago Manual of Style (17th edition)

ucin1396532622
598
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This open access ETD is published by University of Cincinnati and OhioLINK.