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Decreasing Distortion Energies without Strain: Diazo-Selective 1,3-Dipolar Cycloadditions

The diazo group has attributes that complement those of the azido group for applications in chemical biology. Here, we use computational analyses to provide insights into the chemoselectivity of the diazo group in 1,3-dipolar cycloadditions. Dipole distortion energies are responsible for ~80% of the...

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Detaylı Bibliyografya
Yayımlandı:J Org Chem
Asıl Yazarlar: Gold, Brian, Aronoff, Matthew R., Raines, Ronald T.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2016
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5141247/
https://ncbi.nlm.nih.gov/pubmed/27332711
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/acs.joc.6b00948
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