Connecting a carbonyl and a π-conjugated group through a -phenylene linker by (5+1) benzene ring formation
A benzene ring was formed to connect a carbonyl group of various methyl ketones with a π-conjugated group through a p -phenylene linker. Methyl ketones and streptocyanines were used as the C1 and C5 sources, respectively, in the (5+1) annulation, which could form donor-π-acceptor molecules. A benzen...
Saved in:
Published in | Chemical communications (Cambridge, England) Vol. 55; no. 59; pp. 8575 - 8578 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
18.07.2019
|
Online Access | Get full text |
Cover
Loading…
Summary: | A benzene ring was formed to connect a carbonyl group of various methyl ketones with a π-conjugated group through a
p
-phenylene linker. Methyl ketones and streptocyanines were used as the C1 and C5 sources, respectively, in the (5+1) annulation, which could form donor-π-acceptor molecules.
A benzene ring was formed to connect a carbonyl group of various methyl ketones with a π-conjugated group through a
p
-phenylene linker. |
---|---|
Bibliography: | Electronic supplementary information (ESI) available: Experimental procedures and NMR data. See DOI 10.1039/c9cc04012a |
ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c9cc04012a |