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1,3-Dipolar Cycloadditions of Diazo Compounds in the Presence of Azides
The diazo group has untapped utility in chemical biology. The tolerance of stabilized diazo groups to cellular metabolism is comparable to that of azido groups. Yet, chemoselectivity has been elusive, as both groups undergo 1,3-dipolar cycloadditions with strained alkynes. Removing strain and tuning...
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| Gepubliceerd in: | Org Lett |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
2016
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5141246/ https://ncbi.nlm.nih.gov/pubmed/26981746 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.orglett.6b00278 |
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