Please use this identifier to cite or link to this item:
https://hdl.handle.net/10356/20676
Title: | Asymmetric synthesis of chiral arsine ligands promoted by organopalladium complexes | Authors: | Lim, Maricar Bungabong | Keywords: | DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis DRNTU::Science::Chemistry::Organic chemistry::Organometallic compounds |
Issue Date: | 2008 | Source: | Lim, M. B. (2008). Asymmetric synthesis of chiral arsine ligands promoted by organopalladium complexes. Doctoral thesis, Nanyang Technological University, Singapore. | Abstract: | The bis(acetonitrile) (S) phenanthrylamine palladium II complex (Sc)-116 is used in the [4+2] Diels-Alder cycloaddition reaction between diphenylvinylarsine and DMPP producing two isomeric products in a ratio of 5:1. The bidentate ligand (Sp)-80 is liberated by simple treatment of complex (Rp)-79 with aqueous potassium cyanide. | URI: | https://hdl.handle.net/10356/20676 | DOI: | 10.32657/10356/20676 | Schools: | School of Physical and Mathematical Sciences | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | SPMS Theses |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
MaricarLimBungabong08.pdf | 11.67 MB | Adobe PDF | View/Open |
Page view(s) 10
784
Updated on Mar 26, 2024
Download(s) 20
327
Updated on Mar 26, 2024
Google ScholarTM
Check
Altmetric
Items in DR-NTU are protected by copyright, with all rights reserved, unless otherwise indicated.