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Accessing 2,1-Borazaronaphthols: Self-Arylation of 1-Alkyl-2-aryl-3-bromo-2,1-borazaronaphthalenes

[Image: see text] Unlike their B-alkyl counterparts, brominated N-alkyl B-aryl 2,1-borazaronaphthalenes undergo a self-arylation reaction in the presence of a catalytic amount of palladium and base, in which the azaborine serves as both the electrophile and the nucleophile. The products of the self-...

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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Molander, Gary A., Wisniewski, Steven R.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: American Chemical Society 2014
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4156240/
https://ncbi.nlm.nih.gov/pubmed/25133658
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo501638q
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