The Synthesis and Reactivity of Carbamoyl Fluorides

dc.contributor.advisorLe, Christine
dc.contributor.authorTiburcio, Tristan Redondo
dc.date.accessioned2022-12-14T16:35:34Z
dc.date.available2022-12-14T16:35:34Z
dc.date.copyright2022-07-28
dc.date.issued2022-12-14
dc.date.updated2022-12-14T16:35:34Z
dc.degree.disciplineChemistry
dc.degree.levelMaster's
dc.degree.nameMSc - Master of Science
dc.description.abstractChapter 1 Herein we report a protocol for the synthesis of carbamoyl fluorides from secondary amines using inexpensive, and commercially available starting materials. This method employs the use of a difluorocarbene generated from the thermolysis of (triphenylphosphonio)difluoroacetate. This becomes oxidized by 4-methylpyridine N-oxide, generating difluorophosgene, which serves as the key intermediate to make the carbamoyl fluorides from secondary amine starting materials. This method allows access to carbamoyl fluorides with a vast functional group tolerance, including Lewis-basic heterocycles, alkenes, and alkynes. Chapter 2 We report a base-free, facile cross-coupling reaction of carbamoyl fluorides to silylated nucleophiles. This reaction utilizes an affordable and Earth-abundant nickel transition metal catalyst, with a common phenanthroline ligand (both of which see an exceptionally low loading), to synthesize ureas, carbamates, and alkynamides in moderate to excellent yields. The transmetallation step of the purported catalytic cycle generates a fluorosilane, providing the thermodynamic driving force for the reaction to progress, and circumventing the requirement of base.
dc.identifier.urihttp://hdl.handle.net/10315/40718
dc.languageen
dc.rightsAuthor owns copyright, except where explicitly noted. Please contact the author directly with licensing requests.
dc.subjectChemistry
dc.subject.keywordsCarbamoyl fluorides
dc.subject.keywordsSynthesis
dc.subject.keywordsCross-coupling
dc.subject.keywordsNickel-catalyzed
dc.titleThe Synthesis and Reactivity of Carbamoyl Fluorides
dc.typeElectronic Thesis or Dissertation

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Tiburcio_Tristan_R_2022_Masters.pdf
Size:
2.37 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 2 of 2
No Thumbnail Available
Name:
license.txt
Size:
1.87 KB
Format:
Plain Text
Description:
No Thumbnail Available
Name:
YorkU_ETDlicense.txt
Size:
3.39 KB
Format:
Plain Text
Description:

Collections