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- W2016648982 abstract "Viel stärker als die Bishomoaromatizität des Urahns 1 aller Homoarene ist die der Dianionen 2 von 1,2,4-Triboracyclopentanen, deren Gerüst isoelektronisch ist mit dem des experimentell unbekannten monocyclischen Prototyps 3. Donorsubstituenten R, die die Homoaromatizität von 1 (und erst recht die von 3) aufheben, sind bei 2 nahezu wirkungslos. Dur=2,3,5,6-Tetramethylphenyl; R=Me, Ph, OEt, NEt2." @default.
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- W2016648982 date "2000-04-03" @default.
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- W2016648982 title "Bishomoaromatische Dianionen von 1,2,4-Triboracyclopentanen: starke Dreizentren-Zweielektronen-Bindungen zwischen drei Boratomen" @default.
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- W2016648982 doi "https://doi.org/10.1002/(sici)1521-3757(20000403)112:7<1329::aid-ange1329>3.0.co;2-j" @default.
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