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Synthesis 2017; 49(01): 17-28
DOI: 10.1055/s-0035-1562623
DOI: 10.1055/s-0035-1562623
short review
Vicinal Tricarbonyl Compounds: Versatile Building Blocks for Natural Product Synthesis
Weitere Informationen
Publikationsverlauf
Received: 12. Juni 2016
Accepted after revision: 22. Juli 2016
Publikationsdatum:
22. August 2016 (online)
Dedicated to Prof. Dieter Enders on the occasion of his 70th birthday
Abstract
Due to their high density of functional groups, vicinal tricarbonyl compounds are versatile building blocks for the synthesis of complex target molecules. Methods for their preparation and their use in stereoselective C–C bond formations, as well as for the synthesis of heteroaromatics, are summarised for the period 2006–2016. Several examples for their applications in natural product synthesis (awajanomycin, cladoniamide, wailupemycin) are presented.
1 Introduction
2 Preparation of Vicinal Tricarbonyl Compounds
3 Use in Stereoselective C–C Bond Formations
4 Use for the Synthesis of Heteroaromatics
5 Examples from Natural Product Synthesis
6 Conclusion
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