A new and efficient synthesis of indenone

Zengin, Mustafa; Balci, Mustafa

dc.contributor.authors	Zengin, M; Dastan, A; Balci, M;
dc.date.accessioned	2020-02-24T14:15:04Z
dc.date.available	2020-02-24T14:15:04Z
dc.date.issued	2001
dc.identifier.citation	Zengin, M; Dastan, A; Balci, M; (2001). A new and efficient synthesis of indenone. SYNTHETIC COMMUNICATIONS, 31, 1999-1993
dc.identifier.issn	0039-7911
dc.identifier.uri	https://hdl.handle.net/20.500.12619/44839
dc.identifier.uri	https://doi.org/10.1081/SCC-100104416
dc.description.abstract	Reaction of dichloroketone 2 with NEt3 gave indenone (4) in high yield. Catodic reaction of 2 in the presence of C/Pt electrodes afforded the rearranged product 3 in high yield besides a small amount of chlorohydroxyketone 5. Reaction of rearranged dichloroketone 3 with NEt3 provided indenone (4) as the sole product. The mechanism of these reaction was discussed.
dc.language	English
dc.publisher	MARCEL DEKKER INC
dc.subject	Chemistry
dc.title	A new and efficient synthesis of indenone
dc.type	Article
dc.identifier.volume	31
dc.identifier.startpage	1993
dc.identifier.endpage	1999
dc.contributor.department	Sakarya Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü
dc.contributor.saüauthor	Zengin, Mustafa
dc.contributor.saüauthor	Balci, Mustafa
dc.relation.journal	SYNTHETIC COMMUNICATIONS
dc.identifier.wos	WOS:000170129700008
dc.contributor.author	Zengin, Mustafa
dc.contributor.author	Balci, Mustafa