Access to NH-aziridine-2-carboxamides through Davidsen acylimidodicarbonate activation
Comptes Rendus Chimie, ISSN: 1631-0748, Vol: 22, Issue: 4, Page: 283-293
2019
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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.
Article Description
Acylimidodicarbonates obtained from aziridine-2-carboxamides through Davidsen bis-Boc activation react with amine nucleophiles under mild conditions to form tertiary aziridine-2-carboxylic acid amides. NH aziridine-2-carboxylic acid amides were obtained by hydrogenolythic deprotection of N-Cbz derivatives.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1631074819300402; http://dx.doi.org/10.1016/j.crci.2019.03.001; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85064240426&origin=inward; https://comptes-rendus.academie-sciences.fr/chimie/articles/10.1016/j.crci.2019.03.001/; https://dx.doi.org/10.1016/j.crci.2019.03.001
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