Highly enantioselective nitrone cycloadditions with 2-alkenoyl pyridine N-oxides catalyzed by Cu
Organic Letters, ISSN: 1523-7060, Vol: 13, Issue: 3, Page: 402-405
2011
- 49Citations
- 22Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations49
- Citation Indexes49
- CrossRef49
- 48
- Captures22
- Readers22
- 22
Article Description
Enantioselective nitrone cycloadditions with 2-alkenoyl pyridine N-oxides as dipolarophiles have been reported. The reaction is catalyzed by Cu (II)-BOX complexes to give the expected isoxazolidine products with high diastereo-and enantioselectivity. © 2011 American Chemical Society.
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