Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Chiral Birch reduced tertiary phosphines: precursors to asymmetric 1,2-cyclohexenebis(tertiary phosphines)

Thumbnail Image

Date

2010

Authors

Bulbrook, Michelle
Chu, Minghui
Deane, Karen
Doyle, Roy
Hinc, Justina
Petersen, Charlotte
Salem, Geoffrey
Thorman, Nadia
Willis, Anthony

Journal Title

Journal ISSN

Volume Title

Publisher

Royal Society of Chemistry

Abstract

The first examples of an optically active Birch reduced tertiary phosphine, viz. (RP)-(cyclohexa-2,5-dienyl)(3-pentyl)phenylphosphine, and successful hydrophosphination of the related racemic ligand (±)- (cyclohexa-2,5-dienyl)(2-propyl)phenylphosphine wi

Description

Keywords

Keywords: Crystal structure determination; Cyclohexenes; Hydrophosphination; Optically Active; Phenylphosphines; Racemic ligands; Tertiary phosphines; Olefins; Palladium; Palladium compounds; Phosphorus compounds; Platinum; Semiconducting indium gallium arsenide; C

Citation

URI

http://hdl.handle.net/1885/60673

Collections

ANU Research Publications

Source

Dalton Transactions

Type

Journal article

Book Title

Entity type

Access Statement

License Rights

DOI

10.1039/c0dt00648c

Restricted until

2037-12-31

Downloads

File
Description
01_Bulbrook_Chiral_Birch_reduced_tertiary_2010.pdf (306.57 KB)

DSpace software copyright © 2002-2026 LYRASIS

abcd