Abstract
A series of cyclometallated gold(III) complexes [Au(CN)Cl2] 1a-l (HCN=arylpyridines) and a PEG-linked complex 1m were synthesized. Complexes 1a-m are effective in catalyzing the synthesis of propargylic amines, chiral allenes and isoxazoles. Six-membered ring cyclometallated gold(III) complexes 1f-l exhibited higher catalytic activity than five-membered ring cyclometallated gold(III) complexes 1a-e. The diastereoselectivity of propargylic amines could be tuned by using chiral aldehyde and/or amine substrates. Excellent enantioselectivities (90-98% ee) were achieved in chiral allene synthesis. Chiral allene racemization could be minimized by using 1f as catalyst. The PEG-linked catalyst 1m is the most catalytically active towards synthesis of propargylic amines, in which case a product turnover of 900 was achieved. Moreover, 1m could be repeatedly used for 12 reaction cycles, leading to an overall turnover number of 872.
| Original language | English |
|---|---|
| Pages (from-to) | 2055-2070 |
| Number of pages | 16 |
| Journal | Advanced Synthesis and Catalysis |
| Volume | 355 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - 8 Jul 2013 |
Keywords
- allenes
- cyclometallation
- gold catalysis
- isoxazoles
- propargylic amines
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry