3-SUBSTITUTED 2-CYCLOPENTENONES FROM CYCLOPENTADIENES

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	LIN, CC	en_US
dc.contributor.author	HSIA, KS	en_US
dc.contributor.author	WU, HJ	en_US
dc.date.accessioned	2014-12-08T15:04:15Z	-
dc.date.available	2014-12-08T15:04:15Z	-
dc.date.issued	1993-12-01	en_US
dc.identifier.issn	0009-4536	en_US
dc.identifier.uri	http://hdl.handle.net/11536/2754	-
dc.description.abstract	Oxidation 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.language.iso	en_US	en_US
dc.subject	3-SUBSTITUTED 2-CYCLOPENTENONES	en_US
dc.subject	CYCLOPENTADIENES	en_US
dc.subject	PCC	en_US
dc.title	3-SUBSTITUTED 2-CYCLOPENTENONES FROM CYCLOPENTADIENES	en_US
dc.type	Article	en_US
dc.identifier.journal	JOURNAL OF THE CHINESE CHEMICAL SOCIETY	en_US
dc.citation.volume	40	en_US
dc.citation.issue	6	en_US
dc.citation.spage	587	en_US
dc.citation.epage	591	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:A1993MP29300015	-
dc.citation.woscount	1	-
顯示於類別：	期刊論文