Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/15638
Title: Design, synthesis and structure of new chiral squaric acid monoaminoalcohols and diaminoalcohols and their use as catalysts in asymmetric reduction of ketones and diketones
Authors: Zhou, HB
Zhang, J
Lu, SM
Xie, RG
Zhou, ZY
Choi, MCK
Chan, ASC
Yang, TK
Keywords: Asymmetric synthesis
Enantioselective reduction
Prochiral ketones and diketones
Squaric aminoalcohol and diaminoalcohols
Issue Date: 2001
Publisher: Pergamon Press
Source: Tetrahedron, 2001, v. 57, no. 45, p. 9325-9333 How to cite?
Journal: Tetrahedron 
Abstract: Many chiral squaric acid aminoalcohols and C2-symmetric diaminoalcohols have been synthesized and their in situ formed chiral boron heterocycles have been used as catalysts for the enantioselective reduction of prochiral ketones and diketones by borane to give alcohols with up to 99% enantiomeric excess and 99% yield. The effects of solvent, catalyst-substrate ratio and temperature were also investigated.
URI: http://hdl.handle.net/10397/15638
ISSN: 0040-4020
DOI: 10.1016/S0040-4020(01)00936-X
Appears in Collections:Journal/Magazine Article

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

SCOPUSTM   
Citations

25
Last Week
0
Last month
0
Citations as of Jul 23, 2017

WEB OF SCIENCETM
Citations

25
Last Week
0
Last month
0
Citations as of Aug 13, 2017

Page view(s)

35
Last Week
1
Last month
Checked on Aug 14, 2017

Google ScholarTM

Check

Altmetric



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