Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101515
PIRA download icon_1.1View/Download Full Text
DC FieldValueLanguage
dc.contributorDepartment of Applied Biology and Chemical Technologyen_US
dc.creatorHe, Jen_US
dc.creatorLam, SMen_US
dc.creatorNg, JPLen_US
dc.creatorWong, WTen_US
dc.creatorChiu, Pen_US
dc.date.accessioned2023-09-18T07:30:36Z-
dc.date.available2023-09-18T07:30:36Z-
dc.identifier.issn1001-8417en_US
dc.identifier.urihttp://hdl.handle.net/10397/101515-
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.rights© 2019 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.en_US
dc.rights© 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.rightsThe following publication He, J., Lam, S. M., Ng, J. P., Wong, W. T., & Chiu, P. (2019). Intramolecular (4 + 3) cycloadditions of nitrogen-tethered epoxy enosilanes for the synthesis of heteropolycycles. Chinese Chemical Letters, 30(8), 1523-1526 is available at https://doi.org/10.1016/j.cclet.2019.04.051.en_US
dc.subject(4 + 3) cycloadditionen_US
dc.subjectEpoxidesen_US
dc.subjectFuranen_US
dc.subjectHeterocyclesen_US
dc.subjectIntramolecularen_US
dc.subjectPiperidineen_US
dc.subjectPolycyclic compoundsen_US
dc.titleIntramolecular (4 + 3) cycloadditions of nitrogen-tethered epoxy enosilanes for the synthesis of heteropolycyclesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1523en_US
dc.identifier.epage1526en_US
dc.identifier.volume30en_US
dc.identifier.issue8en_US
dc.identifier.doi10.1016/j.cclet.2019.04.051en_US
dcterms.abstractFurans bearing epoxy enolsilane units via a tether that incorporates a nitrogen heteroatom, undergo intramolecular (4 + 3) cycloadditions to generate bis-heteroatomic polycyclic adducts having piperidine moieties in their frameworks. The cycloadducts, ultimately derived from furfural, a renewal chemical feedstock, are obtained with up to 4:1 dr and with ee retained from the epoxide.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationChinese chemical letters, Aug. 2019, v. 30, no. 8, p. 1523-1526en_US
dcterms.isPartOfChinese chemical lettersen_US
dcterms.issued2019-08-
dc.identifier.scopus2-s2.0-85065236399-
dc.description.validate202308 bckwen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0368-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe State Key Laboratory of Synthetic Chemistry; The University of Hong Kongen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS25503984-
dc.description.oaCategoryGreen (AAM)en_US
Appears in Collections:Journal/Magazine Article
Files in This Item:
File Description SizeFormat 
Wong_Intramolecular_Cycloadditions_Nitrogen-Tethered.pdfPre-Published version900.35 kBAdobe PDFView/Open
Open Access Information
Status open access
File Version Final Accepted Manuscript
Access
View full-text via PolyU eLinks SFX Query
Show simple item record

Page views

71
Citations as of Apr 14, 2025

Downloads

56
Citations as of Apr 14, 2025

SCOPUSTM   
Citations

3
Citations as of Dec 19, 2025

WEB OF SCIENCETM
Citations

1
Citations as of Oct 10, 2024

Google ScholarTM

Check

Altmetric


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