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Quinazolinone Synthesis through Base-Promoted S(N)Ar Reaction of ortho-Fluorobenzamides with Amides Followed by Cyclization
[Image: see text] A transition-metal-free synthesis of quinazolin-4-ones by Cs(2)CO(3)-promoted S(N)Ar reaction of ortho-fluorobenzamides with amides followed by cyclization in dimethyl sulfoxide has been developed. The present procedure can provide efficient synthetic methods for the formation of b...
Tallennettuna:
| Julkaisussa: | ACS Omega |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
American Chemical Society
2019
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| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6647956/ https://ncbi.nlm.nih.gov/pubmed/31459909 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acsomega.9b00699 |
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