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The 9H‐9‐Borafluorene Dianion: A Surrogate for Elusive Diarylboryl Anion Nucleophiles

Double reduction of the THF adduct of 9H‐9‐borafluorene (1⋅THF) with excess alkali metal affords the dianion salts M(2)[1] in essentially quantitative yields (M=Li–K). Even though the added charge is stabilized through π delocalization, [1](2−) acts as a formal boron nucleophile toward organoboron (...

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Bibliografske podrobnosti
izdano v:Angew Chem Int Ed Engl
Main Authors: Gilmer, Jannik, Budy, Hendrik, Kaese, Thomas, Bolte, Michael, Lerner, Hans‐Wolfram, Wagner, Matthias
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2020
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7155136/
https://ncbi.nlm.nih.gov/pubmed/31834978
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/anie.201914219
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