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Tandem synthesis of 1-formyl-1,2,3-triazoles
A tandem method for preparing 4-formyl-1,2,3-triazoles via a two-step one-pot acetal cleavage/CuAAC reaction was developed. Using this method, 4-formyl-1,2,3-triazole analogs with both electron-withdrawing and electron-donating substituents were prepared in good yield and purity. Expansion of this m...
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| Izdano u: | Tetrahedron Lett |
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| Glavni autori: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2017
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5798646/ https://ncbi.nlm.nih.gov/pubmed/29422697 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.tetlet.2017.10.023 |
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