This submission belongs to the session a. General Organic Synthesis of the event The 8th International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Nov, 2004
Citation
Tuyen Nguyen Van, Matthias D’Hooghe, Siegfried Pattyn, Norbert De Kimpe, Application of Ring Closing Metathesis Towards Functionalized 1,4-dihydro-9,10-anthraquinones and Anthraquinones Using Grubbs’ Catalyst, in Proceedings of The 8th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2004, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-8-01951
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Application of Ring Closing Metathesis Towards Functionalized 1,4-dihydro-9,10-anthraquinones and Anthraquinones Using Grubbs’ Catalyst
Tuyen Nguyen Van 1
Matthias D’Hooghe 1
Siegfried Pattyn 1
Norbert De Kimpe 1
1. Department of Organic Chemistry, Faculty of Bioscience Engineering, Ghent University, Coupure links 653, B-9000 Ghent, Belgium
Abstract
A general and straightforward synthesis of anthraquinones was developed, in which diallylation of 1,4-naphthoquinones, followed by Ring Closing Metathesis (RCM) of the resulting diallylnaphthoquinones with Grubbs’ catalyst and subsequent dehydrogenation using Pd/C afforded the desired anthraquinones with regio control of substituents and in good yields.
Keywords
n/a
2-Nitrofurans as Dienophiles in Diels-Alder Reactions