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Synthesis of ferrocenyl-substituted 1,3-dithiolanes via [3 + 2]-cycloadditions of ferrocenyl hetaryl thioketones with thiocarbonyl S-methanides
Ferrocenyl hetaryl thioketones react smoothly with in situ generated thiocarbonyl S-methanides to give 1,3-dithiolanes. In the case of aromatic S-methanides, the sterically more crowded 4,4,5,5-tetrasubstituted 1,3-dithiolanes (2-CH(2) isomers) were formed as sole products. The reactions with cycloa...
Tallennettuna:
| Julkaisussa: | Beilstein J Org Chem |
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| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Beilstein-Institut
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4979640/ https://ncbi.nlm.nih.gov/pubmed/27559392 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3762/bjoc.12.136 |
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