MS (Master of Science)
Date of Award
Committee Chair or Co-Chairs
David G. J. Young
Yu-Lin Jiang, Jeffrey G. Wardeska
A new approach to fulminic acid cycloadditions has been developed. At reduced temperatures, fulminic acid is generated in situ and undergoes 1, 3-diploar cycloaddition reactions with dipolarophiles to form isoxazolines and/or its dimers. This procedure represents a novel, safe general method for the one-step generation of fulminic acid, which complements existing potentially explosive protocols.
Thesis - Open Access
Toh, Ophilia Ndi, "Synthesis Towards Fulminic Acid and Its Derivatives in 1, 3-Dipolar Cycloaddition Reactions." (2008). Electronic Theses and Dissertations. Paper 1982. http://dc.etsu.edu/etd/1982
Copyright by the authors.