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A new and efficient synthesis of indenone

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dc.contributor.authors Zengin, M; Dastan, A; Balci, M;
dc.date.accessioned 2020-01-15T06:46:19Z
dc.date.available 2020-01-15T06:46:19Z
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/20.500.12619/3913
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


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