期刊
ORGANIC LETTERS
卷 15, 期 13, 页码 3334-3337出版社
AMER CHEMICAL SOC
DOI: 10.1021/ol4013734
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资金
- Stellenbosch University
- Sasol
- Harry Crossley Foundation
- Commonwealth Scholarship
The sense of asymmetric ortholithiation directed by a chiral oxazoline may be inverted simply by the choice of achiral ligand. Comparison of results with a number of ferrocenyl oxazoline derivatives suggests that lithiation takes place by coordination to the oxazoline nitrogen irrespective of the ligand used.
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