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@article{Glöcklhofer:2018:10.1080/00397911.2018.1483027,
author = {Glöcklhofer, F and Stöger, B and Fröhlich, J},
doi = {10.1080/00397911.2018.1483027},
journal = {Synthetic Communications},
pages = {2358--2365},
title = {Synthesis of 1,2,5,6- and 1,4,5,8-anthracenetetrone: Building blocks for π-conjugated small molecules and polymers},
url = {http://dx.doi.org/10.1080/00397911.2018.1483027},
volume = {48},
year = {2018}
}

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TY  - JOUR
AB  - Reliable reactions for the synthesis of two interesting anthracenetetrones have been identified and optimized. Both syntheses start from dihydroxy-9,10-anthraquinones and were selected for maximized efficiency and minimized work load. Work-up of all reactions can be achieved without column chromatography, which facilitates further scale-up. So far, both target compounds are considerably underexplored despite their promising molecular structure for use in devices and in organic synthesis, especially as building blocks for π-conjugated compounds. The crystal structure of 1,4,5,8-anthracentetrone is reported.
AU  - Glöcklhofer,F
AU  - Stöger,B
AU  - Fröhlich,J
DO  - 10.1080/00397911.2018.1483027
EP  - 2365
PY  - 2018///
SN  - 0039-7911
SP  - 2358
TI  - Synthesis of 1,2,5,6- and 1,4,5,8-anthracenetetrone: Building blocks for π-conjugated small molecules and polymers
T2  - Synthetic Communications
UR  - http://dx.doi.org/10.1080/00397911.2018.1483027
UR  - http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000449530700005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
UR  - https://www.tandfonline.com/doi/full/10.1080/00397911.2018.1483027
UR  - http://hdl.handle.net/10044/1/72582
VL  - 48
ER  -

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Dr Florian Glöcklhofer

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