Return to search

Development of 1,4-Azaborine-Derived Biaryl Phosphine Ligands with P-central and Axial Chirality:

Thesis advisor: Shih-Yuan Liu / New P-central and axially chiral 1,4-azaborine-derived biaryl phosphine Senphos ligand were designed and synthesized. The separation of diastereomers and enantiomers of those ligands was achieved through preparative recycling HPLC, and the separation efficiency was increased via the use of a borane protecting group. The effect of solvents and diamine ligands in enantioselective ligand synthesis was examined. The absolute configuration of the key enantiomer was confirmed via X-ray crystallography analysis. The catalytic performance of these newly synthesized ligands was evaluated through several benchmark reactions, demonstrating their potential in enantioselective catalysis. / Thesis (MS) — Boston College, 2024. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.

Identiferoai:union.ndltd.org:BOSTON/oai:dlib.bc.edu:bc-ir_110096
Date January 2024
CreatorsHuang, Kaiyun
PublisherBoston College
Source SetsBoston College
LanguageEnglish
Detected LanguageEnglish
TypeText, thesis
Formatelectronic, application/pdf
RightsCopyright is held by the author, with all rights reserved, unless otherwise noted.

Page generated in 0.0022 seconds