Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/20104
Title: A convenient, one-step synthesis of optically active tertiary aminonaphthol and its applications in the highly enantioselective alkenylations of aldehydes
Authors: Ji, JX
Qiu, LQ
Yip, WC
Chan, ASC
Issue Date: 2003
Publisher: American Chemical Society
Source: Journal of organic chemistry, 2003, v. 68, no. 4, p. 1589-1590 How to cite?
Journal: Journal of organic chemistry 
Abstract: Optically active tertiary aminonaphthol 1 was obtained by a new, convenient procedure and was found to catalyze the enantioselective alkenylation of various aldehydes with high ee values, which provides a practical method for the synthesis of chiral (E)- allyl alcohols.
URI: http://hdl.handle.net/10397/20104
ISSN: 0022-3263
EISSN: 1520-6904
DOI: 10.1021/jo026551k
Appears in Collections:Journal/Magazine Article

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

SCOPUSTM   
Citations

97
Last Week
0
Last month
2
Citations as of Aug 11, 2017

WEB OF SCIENCETM
Citations

90
Last Week
0
Last month
0
Citations as of Aug 13, 2017

Page view(s)

33
Last Week
1
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.