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Metal-free, photoinduced remote C(sp(3))–H borylation
Here, we describe a protocol for the metal-free, photo-induced borylation of unactivated C(sp(3))–H bonds distal to an O-oxalate hydroxamic ester functionality. The methodology requires only substrate and bis(catecholato)diboron under light irradiation to effect the desired transformation. A range o...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10498503/ https://www.ncbi.nlm.nih.gov/pubmed/37712044 http://dx.doi.org/10.1039/d3sc03048b |
Sumario: | Here, we describe a protocol for the metal-free, photo-induced borylation of unactivated C(sp(3))–H bonds distal to an O-oxalate hydroxamic ester functionality. The methodology requires only substrate and bis(catecholato)diboron under light irradiation to effect the desired transformation. A range of linear and cyclic tertiary and secondary borylation products are obtained in good yields and high site-selectivity enabling the late-stage C(sp(3))–H borylation of natural product derivatives and drug-like compounds. |
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