This submission belongs to the session a. General Organic Synthesis of the event The 9th International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Nov, 2005
Citation
Pascal Habonimana, Sven Claessens, Norbert De Kimpe, The Use of the Stille Cross-Coupling Reaction in the Prenylation of Naphthoquinones, in Proceedings of The 9th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2005, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-9-01485
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The Use of the Stille Cross-Coupling Reaction in the Prenylation of Naphthoquinones
Pascal Habonimana 1
Sven Claessens 1
Norbert De Kimpe 1
1. Department of Organic Chemistry, Faculty of Bioscience Engineering, Ghent University, Belgium
Abstract
Prenylation reactions are important reactions in natural product chemistry. The Stille reaction was evaluated for the prenylation of naphthoquinones and applied to the synthesis of the natural product 2,3-bis-(3-methylbut-2-enyl)-1,4-naphthoquinone.
Keywords
naphthoquinones
prenylation
Stille reaction
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