Synthetic Applications of Oxidative Aromatic Coupling : From Biphenols to Nanographenes

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dc.identifier.uri Grzybowski, Marek Sadowski, Bartłomiej Butenschön, Holger Gryko, Daniel T. 2021-05-19T05:33:09Z 2021-05-19T05:33:09Z 2019
dc.identifier.citation Grzybowski, M.; Sadowski, B.; Butenschön, H.; Gryko, D.T.: Synthetic Applications of Oxidative Aromatic Coupling : From Biphenols to Nanographenes. In: Angewandte Chemie - International Edition 59 (2019), Nr. 8, S. 2998-3027. DOI:
dc.description.abstract Oxidative aromatic coupling occupies a fundamental place in the modern chemistry of aromatic compounds. It is a method of choice for the assembly of large and bewildering architectures. Considerable effort was also devoted to applications of the Scholl reaction for the synthesis of chiral biphenols and natural products. The ability to form biaryl linkages without any prefunctionalization provides an efficient pathway to many complex structures. Although the chemistry of this process is only now becoming fully understood, this reaction continues to both fascinate and challenge researchers. This is especially true for heterocoupling, that is, oxidative aromatic coupling with the chemoselective formation of a C−C bond between two different arenes. Analysis of the progress achieved in this field since 2013 reveals that many groups have contributed by pushing the boundary of structural possibilities, expanding into surface‐assisted (cyclo)dehydrogenation, and developing new reagents. eng
dc.language.iso eng
dc.publisher Weinheim : Wiley-VCH Verlag
dc.relation.ispartofseries Angewandte Chemie - International Edition 59 (2019), Nr. 8
dc.rights CC BY 4.0 Unported
dc.subject biaryls eng
dc.subject Lewis acids eng
dc.subject nanographenes eng
dc.subject oxidative coupling eng
dc.subject Scholl reaction eng
dc.subject.ddc 540 | Chemie ger
dc.title Synthetic Applications of Oxidative Aromatic Coupling : From Biphenols to Nanographenes
dc.type Article
dc.type Text
dc.relation.essn 1521-3773
dc.relation.issn 0570-0833
dc.relation.issn 1433-7851
dc.bibliographicCitation.issue 8
dc.bibliographicCitation.volume 59
dc.bibliographicCitation.firstPage 2998
dc.bibliographicCitation.lastPage 3027
dc.description.version publishedVersion
tib.accessRights frei zug�nglich

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