Abstract
The Michael reaction of substituted isorhodanines with α,β-unsaturated aldehydes in the presence of a catalytic amount of a chiral secondary amine is presented. This transformation proceeds in good to high yields furnishing the corresponding 4,5-disubstituted isorhodanine adducts in good to excellent enantioselectivities.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 3926-3933 |
| Number of pages | 8 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 14 |
| Issue number | 16 |
| DOIs | |
| State | Published - Apr 28 2016 |
| Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
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