Regio- and enantioselective allylic substitution with less active N- or O-nucleophiles catalyzed by iridium-complex of bis(oxazolinyl)pyridine
Chemical and Pharmaceutical Bulletin, ISSN: 0009-2363, Vol: 59, Issue: 6, Page: 714-720
2011
- 11Citations
- 8Captures
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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.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations11
- Citation Indexes11
- 11
- CrossRef8
- Captures8
- Readers8
Article Description
The utility of hydroxylamines as nitrogen nucleophiles was investigated in the iridium-catalyzed regio- and enantioselective allylic substitution. Allylic substitution with hydroxylamines proceeded with good enantioselectivities by using the iridium-complex of bis(oxazolinyl)pyridine ligand. The good regio- and enantioselectivities were also achieved in the reaction with alkylamines, p-anisidine, and 4-methoxyphenol. © 2011 Pharmaceutical Society of Japan.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79957807862&origin=inward; http://dx.doi.org/10.1248/cpb.59.714; http://www.ncbi.nlm.nih.gov/pubmed/21628906; http://www.jstage.jst.go.jp/article/cpb/59/6/59_6_714/_article; https://www.jstage.jst.go.jp/article/cpb/59/6/59_6_714/_article/-char/en/; https://www.jstage.jst.go.jp/article/cpb/59/6/59_6_714/_article/-char/ja/; https://dx.doi.org/10.1248/cpb.59.714; https://www.jstage.jst.go.jp/article/cpb/59/6/59_6_714/_article
Pharmaceutical Society of Japan
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