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Can acyclic conformational control be achieved via a sulfur–fluorine gauche effect?
The gauche conformation of the 1,2-difluoroethane motif is known to involve stabilising hyperconjugative interactions between donor (bonding, σ(C–H)) and acceptor (antibonding, σ*C–F) orbitals. This model rationalises the generic conformational preference of F–C(β)–C(α)–X systems (φ(FCCX) ≈ 60°), wh...
Tallennettuna:
| Julkaisussa: | Chem Sci |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Royal Society of Chemistry
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5659174/ https://ncbi.nlm.nih.gov/pubmed/29511517 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c5sc00871a |
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