Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/108920
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Applied Biology and Chemical Technology | en_US |
| dc.creator | Shi, J | en_US |
| dc.creator | Zhu, Z | en_US |
| dc.creator | Yang, Z | en_US |
| dc.creator | Lin, Y | en_US |
| dc.creator | Yu, T | en_US |
| dc.creator | Zhong, M | en_US |
| dc.creator | Lo, TWB | en_US |
| dc.creator | Chen, X | en_US |
| dc.creator | Luan, T | en_US |
| dc.date.accessioned | 2024-09-10T06:06:38Z | - |
| dc.date.available | 2024-09-10T06:06:38Z | - |
| dc.identifier.issn | 1523-7060 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/108920 | - |
| dc.language.iso | en | en_US |
| dc.publisher | American Chemical Society | en_US |
| dc.rights | © 2024 American Chemical Society | en_US |
| dc.rights | This document is the Accepted Manuscript version of a Published Work that appeared in final form in Organic Letters, copyright © 2024 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.orglett.4c00006. | en_US |
| dc.title | In situ activation of azaarenes and terminal alkynes to construct bridged polycyclic compounds containing isoquinolinones | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 2002 | en_US |
| dc.identifier.epage | 2006 | en_US |
| dc.identifier.volume | 26 | en_US |
| dc.identifier.issue | 10 | en_US |
| dc.identifier.doi | 10.1021/acs.orglett.4c00006 | en_US |
| dcterms.abstract | A copper-catalyzed [4+2] cyclization reaction of isoquinolines and alkynes is developed for the one-step construction of isoquinolinone derivatives with multisubstituted bridging rings. The unique feature of this three-component tandem cyclization reaction is the functionalization of the C1, N2, C3, and C4 positions of 3-haloisoquinolines via the construction of new C–N, C═O, and C–C bonds. This dearomatization strategy for the synthesis of structurally complex isoquinolinone-bridged cyclic compounds offers good chemoselectivity, broad functional group compatibility, greenness, and high step economy. | en_US |
| dcterms.accessRights | open access | en_US |
| dcterms.bibliographicCitation | Organic letters, 15 Mar. 2024, v. 26, no. 10, p. 2002-2006 | en_US |
| dcterms.isPartOf | Organic letters | en_US |
| dcterms.issued | 2024-03-15 | - |
| dc.identifier.scopus | 2-s2.0-85186199509 | - |
| dc.identifier.pmid | 38394378 | - |
| dc.identifier.eissn | 1523-7052 | en_US |
| dc.description.validate | 202409 bcch | en_US |
| dc.description.oa | Accepted Manuscript | en_US |
| dc.identifier.FolderNumber | a3170 | - |
| dc.identifier.SubFormID | 49723 | - |
| dc.description.fundingSource | RGC | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.description.oaCategory | Green (AAM) | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| Shi_Situ_Activation_Azaarenes.pdf | Pre-Published version | 1.11 MB | Adobe PDF | View/Open |
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