Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/19925
Title: Modified BINAPO ligands for Rh-catalysed enantioselective hydrogenation of acetamidoacrylic acids and esters
Authors: Guo, R
Au Yeung, TTL
Wu, J
Choi, MCK
Chan, ASC
Issue Date: 2002
Publisher: Pergamon Press
Source: Tetrahedron : asymmetry, 2002, v. 13, no. 23, p. 2519-2522 How to cite?
Journal: Tetrahedron : asymmetry 
Abstract: (S)- and (R)-2,2′-Bis[bis(3,5-dimethylphenyl)phosphinoyl]-5,5′,6, 6′,7,7′,8,8′-octahydro-1,1′-binaphthyl (Xyl-H8-BINAPO) were synthesised by reacting chlorobis(3,5-dimethylphenyl)phosphine with (S)- and (R)-2,2′-dihydroxyl-5,5′,6,6′,7,7′,8,8′- octahydro-1,1′-binaphthyl, respectively. The applications of these ligands and their corresponding parent analogues in the Rh-catalysed asymmetric hydrogenation of a variety of acetamidoacrylic acids and esters provided chiral amino acid derivatives with good to excellent ee's (up to 97%).
URI: http://hdl.handle.net/10397/19925
ISSN: 0957-4166
EISSN: 1362-511X
DOI: 10.1016/S0957-4166(02)00650-X
Appears in Collections:Journal/Magazine Article

Access
View full-text via PolyU eLinks SFX Query
Show full item record

SCOPUSTM   
Citations

16
Last Week
0
Last month
0
Citations as of Aug 10, 2017

WEB OF SCIENCETM
Citations

15
Last Week
0
Last month
0
Citations as of Aug 12, 2017

Page view(s)

47
Last Week
2
Last month
Checked on Aug 13, 2017

Google ScholarTM

Check

Altmetric



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.