3-SUBSTITUTED 2-CYCLOPENTENONES FROM CYCLOPENTADIENES

Simple item page
dc.citation.epage591en_US
dc.citation.issue6en_US
dc.citation.spage587en_US
dc.citation.volume40en_US
dc.citation.woscount1
dc.contributor.authorLIN, CCen_US
dc.contributor.authorHSIA, KSen_US
dc.contributor.authorWU, HJen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2014-12-08T15:04:15Z
dc.date.available2014-12-08T15:04:15Z
dc.date.issued1993-12-01en_US
dc.description.abstractOxidation of cyclopentadienes 1a-1j, which were prepared by alkylation of cyclopentadienyl anion with the corresponding alkyl bromides, with pyridinium chlorochromate (PCC) gave the 2-cyclopentenones 2a-2j respectively in 10-15% yields. Reaction of 3 and 5 with PCC gave the spiro compounds 4 and 6 respectively in 75-80% yields.en_US
dc.identifier.issn0009-4536en_US
dc.identifier.journalJOURNAL OF THE CHINESE CHEMICAL SOCIETYen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/2754
dc.identifier.wosnumberWOS:A1993MP29300015
dc.language.isoen_USen_US
dc.subject3-SUBSTITUTED 2-CYCLOPENTENONESen_US
dc.subjectCYCLOPENTADIENESen_US
dc.subjectPCCen_US
dc.title3-SUBSTITUTED 2-CYCLOPENTENONES FROM CYCLOPENTADIENESen_US
dc.typeArticleen_US

Files

License bundle

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

Collections

期刊論文;;Articles