Synthesis Towards Fulminic Acid and Its Derivatives in 1, 3-Dipolar Cycloaddition Reactions.

<p>A new approach to fulminic acid cycloadditions has been developed. At reduced temperatures, fulminic acid is generated <em>in situ</em> 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.</p>

Name thesis:degree_name

MS (Master of Science)

Level thesis:degree_level

Thesis - unrestricted

Discipline thesis:degree_discipline

Chemistry

Year dc:date.issued

2008

Author dc:creator

• Toh, Ophilia Ndi

• nitrile oxides
• ploymerization
• cycloaddition
• Isoxazoline
• cycloadducts
• dimerization
• fulminic acid
• Chemistry
• Organic Chemistry
• Physical Sciences and Mathematics

Statement dc:rights

• Copyright by the authors.

Repository record dc:identifier

https://dc.etsu.edu/etd/1982

OAI identifier oai:identifier

oai:dc.etsu.edu:etd-3334