Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/16131
Title: A convenient synthesis of (R)-salmeterol via Rh-catalyzed asymmetric transfer hydrogenation
Authors: Liu, J
Zhou, D
Jia, X
Huang, L
Li, X
Chan, ASC
Issue Date: 2008
Publisher: Pergamon Press
Source: Tetrahedron : asymmetry, 2008, v. 19, no. 15, p. 1824-1828 How to cite?
Journal: Tetrahedron : asymmetry 
Abstract: (R)-Salmeterol was synthesized in eight steps with salicaldehyde as the starting material. The key chiral intermediate, alcohol 5, was prepared via Rh-catalyzed asymmetric transfer hydrogenation with (S,S)-PEG-BsDPEN or (S,S)-TsDPEN ligand and sodium formate as the hydrogen donor under mild conditions.
URI: http://hdl.handle.net/10397/16131
ISSN: 0957-4166
EISSN: 1362-511X
DOI: 10.1016/j.tetasy.2008.07.021
Appears in Collections:Journal/Magazine Article

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

SCOPUSTM   
Citations

23
Citations as of Apr 30, 2016

WEB OF SCIENCETM
Citations

28
Last Week
0
Last month
0
Citations as of Aug 22, 2017

Page view(s)

44
Last Week
0
Last month
Checked on Aug 20, 2017

Google ScholarTM

Check

Altmetric



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