A novel application of cu-pd dual catalyst system for the cross-coupling of styryltrifluoroborates and amides
General Material Designation
[Thesis]
First Statement of Responsibility
Mohammed Shahidul Islam
Subsequent Statement of Responsibility
Al-Masum, Mohammad
.PUBLICATION, DISTRIBUTION, ETC
Name of Publisher, Distributor, etc.
Tennessee State University
Date of Publication, Distribution, etc.
2016
PHYSICAL DESCRIPTION
Specific Material Designation and Extent of Item
104
GENERAL NOTES
Text of Note
Committee members: Karim, Mohammad R.; Okoro, Cosmas; Wang, Xiaofei
NOTES PERTAINING TO PUBLICATION, DISTRIBUTION, ETC.
Text of Note
Place of publication: United States, Ann Arbor; ISBN=978-1-369-13622-7
DISSERTATION (THESIS) NOTE
Dissertation or thesis details and type of degree
M.S.
Discipline of degree
Chemistry
Body granting the degree
Tennessee State University
Text preceding or following the note
2016
SUMMARY OR ABSTRACT
Text of Note
One of the most important transformations in organic synthesis is amidation reaction because of its importance as biomolecules and synthetic products. The amide bond is unique in nature. It stores amino acids to form peptides and proteins. Many nitrogen based functionality can be created into organic systems by forming new C-N bonded organic molecules. The direct amidation reaction by cross-coupling chemistry is a challenge. A Very few works have been reported for this transformation. One of the pioneering ones is reported by Buchwald group where they use palladium catalyzed coupling reaction involving aryl chlorides and acetyl amides. We are interested to see the application of potassium styryltrifluoroborates in cross-coupling with amides, which is yet to be explored. Styryltrifluoroborates and their use in enamides formation by cross-coupling with amides are largely unknown. In this work, a unique, interesting reaction procedure has been developed by using PdCl2(d tbpf)-CuI dual catalyst system for cross-coupling chemistry to form new C-N bonded enamides. It is also a mild, less time consuming and green system employing microwave irradiation. 1H NMR, 13C NMR, 11B NMR and 19F NMR spectra have been analyzed to confirm the synthesized compounds.
TOPICAL NAME USED AS SUBJECT
Organic chemistry
UNCONTROLLED SUBJECT TERMS
Subject Term
Pure sciences;Amidation;Cross-coupling;Dual catalyst;Microwaves