Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/10196
Title: Highly enantioselective 1,4-addition of diethyl phosphite to enones using a dinuclear Zn catalyst
Authors: Zhao, D
Yuan, Y
Chan, ASC
Wang, R
Keywords: Asymmetric catalysis
Enones
Hydrophosphosphonylation
Michael addition
Phosphonates
Issue Date: 2009
Publisher: Wiley-VCH
Source: Chemistry - a European journal, 2009, v. 15, no. 12, p. 2738-2741 How to cite?
Journal: Chemistry - a European journal 
Abstract: Zinc benefits: The first catalytic asymmetric phospha-Michael addition of enones has been developed. Under mild reaction conditions, the γ-oxo phosphonates could be obtained in high yields (up to 99 %) with excellent enantioselectivities (93–99 % ee; see scheme). The strategy makes the asymmetric synthesis of biologically important phosphonate compounds more accessible.
URI: http://hdl.handle.net/10397/10196
ISSN: 0947-6539
EISSN: 1521-3765
DOI: 10.1002/chem.200802688
Appears in Collections:Journal/Magazine Article

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

SCOPUSTM   
Citations

62
Last Week
0
Last month
Citations as of May 17, 2018

WEB OF SCIENCETM
Citations

60
Last Week
1
Last month
2
Citations as of May 25, 2018

Page view(s)

70
Last Week
1
Last month
Citations as of May 21, 2018

Google ScholarTM

Check

Altmetric


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