Abstract
The aldol reaction is one of the most predominantly used reactions for the formation of C-C bonds in synthetic organic chemistry. The vinylogous extension of this fundamental C-C bond-forming reaction, the VMAR, is unique in its atomic economy in the generation of hydroxycarbonyl compounds. The generation of the same hydroxycarbonyl compounds via other routes is sometimes cumbersome and often requires multi-step synthetic sequences. Therefore, the VMAR can be a powerful alternative to other strategies in the rational design of polyketide fragments of complex natural products. In this chapter, recent advances in the VMAR and its applications to natural product synthesis are discussed.
| Original language | English |
|---|---|
| Title of host publication | Modern Methods in Stereoselective Aldol Reactions |
| Publisher | Wiley-VCH Verlag |
| Pages | 83-154 |
| Number of pages | 72 |
| ISBN (Print) | 9783527332052 |
| DOIs | |
| Publication status | Published - 6 Feb 2013 |
Keywords
- Asymmetric
- Butenolides
- D4 donors
- Diastereoselective
- Enantioselective
- Natural product synthesis
- Polyketides
- Vinylogous Mukaiyama aldol reaction
- Vinylogy
ASJC Scopus subject areas
- General Chemistry
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