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Dicationic ring opening reactions of trans-2-phenylcyclopropylamine•HCl: electrophilic cleavage of the distal (C(2)-C(3)) bond of cyclopropanes
Electrophilic ring opening of trans-2-phenylcyclopropylamine•HCl occurs at the distal (C(2)-C(3)) bond. This is consistent with weakening of the distal bond by the σ-withdrawing ammonium group and charge-charge repulsive effects in the transition state.
Kaydedildi:
| Yayımlandı: | J Org Chem |
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| Asıl Yazarlar: | , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2013
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5333643/ https://ncbi.nlm.nih.gov/pubmed/23941589 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo4016198 |
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