File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1002/1521-3773(20011203)40:23<4422::AID-ANIE4422>3.0.CO;2-G
- Scopus: eid_2-s2.0-0035803741
- WOS: WOS:000172626600019
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Enantioseparation of racemic organic molecules by a zeolite Analogue
Title | Enantioseparation of racemic organic molecules by a zeolite Analogue |
---|---|
Authors | |
Keywords | Cadmium Crystal engineering Enantioseparation N ligands Zeolite analogues |
Issue Date | 2001 |
Publisher | Wiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home |
Citation | Angewandte Chemie - International Edition, 2001, v. 40 n. 23, p. 4422-4425 How to Cite? |
Abstract | Selective inclusion of (S)-2-butanol and (S)-2-methyl-1-butanol from their racemic mixtures in 98.2 and 98.4% ee, respectively, is obtained with the robust 3D enantiopure hybrid organic-inorganic zeolite analogue [Cd(QA)2] (see scheme), which is formed by self-assembly of chiral quitenine (HQA) with Cd(OH)2. |
Persistent Identifier | http://hdl.handle.net/10722/70008 |
ISSN | 2023 Impact Factor: 16.1 2023 SCImago Journal Rankings: 5.300 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Xiong, RG | en_HK |
dc.contributor.author | You, XZ | en_HK |
dc.contributor.author | Abrahams, BF | en_HK |
dc.contributor.author | Xue, Z | en_HK |
dc.contributor.author | Che, CM | en_HK |
dc.date.accessioned | 2010-09-06T06:18:51Z | - |
dc.date.available | 2010-09-06T06:18:51Z | - |
dc.date.issued | 2001 | en_HK |
dc.identifier.citation | Angewandte Chemie - International Edition, 2001, v. 40 n. 23, p. 4422-4425 | en_HK |
dc.identifier.issn | 1433-7851 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/70008 | - |
dc.description.abstract | Selective inclusion of (S)-2-butanol and (S)-2-methyl-1-butanol from their racemic mixtures in 98.2 and 98.4% ee, respectively, is obtained with the robust 3D enantiopure hybrid organic-inorganic zeolite analogue [Cd(QA)2] (see scheme), which is formed by self-assembly of chiral quitenine (HQA) with Cd(OH)2. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Wiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home | en_HK |
dc.relation.ispartof | Angewandte Chemie - International Edition | en_HK |
dc.subject | Cadmium | en_HK |
dc.subject | Crystal engineering | en_HK |
dc.subject | Enantioseparation | en_HK |
dc.subject | N ligands | en_HK |
dc.subject | Zeolite analogues | en_HK |
dc.title | Enantioseparation of racemic organic molecules by a zeolite Analogue | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1433-7851&volume=40&spage=4422&epage=4425&date=2001&atitle=Enantioseparation+of+Racemic+Organic+Molecules+by+a+Zeolite+Analogue | en_HK |
dc.identifier.email | Che, CM:cmche@hku.hk | en_HK |
dc.identifier.authority | Che, CM=rp00670 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/1521-3773(20011203)40:23<4422::AID-ANIE4422>3.0.CO;2-G | en_HK |
dc.identifier.scopus | eid_2-s2.0-0035803741 | en_HK |
dc.identifier.hkuros | 111801 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0035803741&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 40 | en_HK |
dc.identifier.issue | 23 | en_HK |
dc.identifier.spage | 4422 | en_HK |
dc.identifier.epage | 4425 | en_HK |
dc.identifier.isi | WOS:000172626600019 | - |
dc.publisher.place | Germany | en_HK |
dc.identifier.scopusauthorid | Xiong, RG=7102951372 | en_HK |
dc.identifier.scopusauthorid | You, XZ=36072101800 | en_HK |
dc.identifier.scopusauthorid | Abrahams, BF=35601898600 | en_HK |
dc.identifier.scopusauthorid | Xue, Z=7203058536 | en_HK |
dc.identifier.scopusauthorid | Che, CM=7102442791 | en_HK |
dc.identifier.issnl | 1433-7851 | - |