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Rationalizing the diverse reactivity of [1.1.1]propellane through σ–π-delocalization

[1.1.1]Propellane is the ubiquitous precursor to bicyclo[1.1.1]pentanes (BCPs), motifs of high value in pharmaceutical and materials research. The classical Lewis representation of this molecule places an inter-bridgehead C–C bond along its central axis; ‘strain relief’-driven cleavage of this bond...

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Detaylı Bibliyografya
Yayımlandı:Chem Sci
Asıl Yazarlar: Sterling, Alistair J., Dürr, Alexander B., Smith, Russell C., Anderson, Edward A., Duarte, Fernanda
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The Royal Society of Chemistry 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC8159217/
https://ncbi.nlm.nih.gov/pubmed/34122945
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/d0sc01386b
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