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A new and efficient synthesis of indenone
Date
2001-01-01
Author
Zengin, M
Dastan, A
Balcı, Metin
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Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
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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.
Subject Keywords
PERHYDROINDAN DERIVATIVES
,
ACIDS
,
RING
URI
https://hdl.handle.net/11511/57623
Journal
SYNTHETIC COMMUNICATIONS
DOI
https://doi.org/10.1081/scc-100104416
Collections
Graduate School of Natural and Applied Sciences, Article
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M. Zengin, A. Dastan, and M. Balcı, “A new and efficient synthesis of indenone,”
SYNTHETIC COMMUNICATIONS
, pp. 1993–1999, 2001, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/57623.