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β-Amino functionalization of cinnamic Weinreb amides in ionic liquid
2-Ns-Protected β-amino Weinreb amides were synthesized by aminochlorination of α,β-unsaturated Weinreb amides in an ionic liquid, 1-n-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide ([BMIM][NTf(2)]). Processed without the use of metal catalysts or the need of an inert gas atmosphere, th...
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| Yayımlandı: | Beilstein J Org Chem |
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| Asıl Yazarlar: | , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Beilstein-Institut
2016
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5238596/ https://ncbi.nlm.nih.gov/pubmed/28144305 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.12.231 |
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