Direct asymmetric reductive amination of α-keto acetals: A platform for synthesizing diverse α-functionalized amines
Chemical Communications, ISSN: 1364-548X, Vol: 58, Issue: 4, Page: 513-516
2022
- 13Citations
- 5Captures
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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
- Citations13
- Citation Indexes13
- 13
- CrossRef12
- Captures5
- Readers5
Article Description
We report an efficient and straightforward method to synthesize enantio-enriched N-unprotected α-amino acetals via ruthenium-catalyzed direct asymmetric reductive amination. The α-amino acetal products are versatile and valuable platform molecules that can be converted to the corresponding α-amino acids, amino alcohols, and other derivatives by convenient transformations.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85122928595&origin=inward; http://dx.doi.org/10.1039/d1cc06601c; http://www.ncbi.nlm.nih.gov/pubmed/34897338; https://xlink.rsc.org/?DOI=D1CC06601C; https://dx.doi.org/10.1039/d1cc06601c; https://pubs.rsc.org/en/content/articlelanding/2022/cc/d1cc06601c
Royal Society of Chemistry (RSC)
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