Abstract
A NHC-promoted cascade reaction between β-methyl enal and dienone is developed for quick access to multicyclic lactone molecules bearing quaternary chiral carbon centers. Our study constitutes the first 1,6-addition of the acylazolium vinyl enolate γ-carbon via NHC catalysis and provides rapid access to complex lactone molecules that are otherwise difficult to prepare. The structurally sophisticated lactone products bearing up to four fused ring structures are afforded in up to quantitative yields with good to excellent enantioselectivities.
Original language | English |
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Pages (from-to) | 2595-2599 |
Number of pages | 5 |
Journal | Organic Letters |
Volume | 22 |
Issue number | 7 |
DOIs | |
Publication status | Published - Apr 3 2020 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:Copyright © 2020 American Chemical Society.
ASJC Scopus Subject Areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry