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Regioselective trans-Carboboration of Propargyl Alcohols
[Image: see text] Proper choice of the base allowed trans-diboration of propargyl alcohols with B(2)(pin)(2) to evolve into an exquisitely regioselective procedure for net trans-carboboration. The method is modular as to the newly introduced carbon substituent (aryl, methyl, allyl, benzyl, alkynyl),...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
American Chemical Society
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727597/ https://www.ncbi.nlm.nih.gov/pubmed/30993987 http://dx.doi.org/10.1021/acs.orglett.9b01225 |