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A one-pot multistep cyclization yielding thiadiazoloimidazole derivatives
A versatile synthetic procedure is described to prepare the benzimidazole-fused 1,2,4-thiadiazoles 2a–c via a methanesulfonyl chloride initiated multistep cyclization involving the intramolecular reaction of an in-situ generated carbodiimide with a thiourea unit. The structure of the intricate heter...
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| Publicat a: | Beilstein J Org Chem |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Beilstein-Institut
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4311674/ https://ncbi.nlm.nih.gov/pubmed/25670969 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.10.317 |
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