<link rel="stylesheet" href="styles.cf390c6bfbe7555f.css"> Skip to main content

Annulation of Benzamides with [60]Fullerene through Palladium(II)-Catalyzed C-H Bond Activation

dc.citation.epage1604en_US
dc.citation.issue6en_US
dc.citation.spage1599en_US
dc.citation.volume76en_US
dc.citation.woscount20
dc.contributor.authorChuang, Shih-Chingen_US
dc.contributor.authorRajeshkumar, Venkatachalamen_US
dc.contributor.authorCheng, Chun-Anen_US
dc.contributor.authorDeng, Jie-Chengen_US
dc.contributor.authorWang, Guan-Wuen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:11:55Z
dc.date.available2014-12-08T15:11:55Z
dc.date.issued2011-03-18en_US
dc.description.abstractPalladium-catalyzed heteroannulation of N-substituted benzamides with [60]fullerene, which proceeds through direct sp(2) C-H bond activation to form 7-membered ring pallada-intermediate with C(60), led to formation of [60]fulleroisoquinolinones in moderate to good yields (8-64% based on recovered C(60)). A plausible reaction pathway is proposed.en_US
dc.identifier.doi10.1021/jo102107ken_US
dc.identifier.issn0022-3263en_US
dc.identifier.journalJOURNAL OF ORGANIC CHEMISTRYen_US
dc.identifier.urihttp://dx.doi.org/10.1021/jo102107ken_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/9139
dc.identifier.wosnumberWOS:000288142800011
dc.language.isoen_USen_US
dc.titleAnnulation of Benzamides with [60]Fullerene through Palladium(II)-Catalyzed C-H Bond Activationen_US
dc.typeArticleen_US

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
000288142800011.pdf
Size:
943.82 KB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed to upon submission
Description: