Projects per year
Abstract
An enantioselective N-heterocyclic carbene (NHC)-catalyzed diene regenerative (4 + 2) annulation has been achieved through the use of highly nucleophilic morpholinone-derived catalysts. The reaction proceeds with good to excellent yields, high enantioselectivity (most >92% ee), and good diastereoselectivity (most >7:1). The generality of the reaction is high, with 19 examples reported. The utility of the products has been examined with subsequent derivatization in Diels–Alder reactions using electron-poor dienophiles. Furthermore, interception of the proposed β-lactone intermediate has been achieved, allowing the synthesis of compounds bearing four contiguous stereocenters with high levels of enantio- and diastereoselectivity.
Original language | English |
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Pages (from-to) | 5332-5335 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 17 |
Issue number | 21 |
DOIs | |
Publication status | Published - 2015 |
Projects
- 2 Finished
-
New Reaction Cascades Exploiting N-Heterocyclic Carbenes.
Australian Research Council (ARC), Monash University
1/01/15 → 31/12/18
Project: Research