Diversity‐Oriented Synthesis of Polycyclic Scaffolds by Modification of an Anodic Product Derived from 2,4‐Dimethylphenol | Zendy

Barjau Joaquin | Zendy; Schnakenburg Gregor | Zendy; Waldvogel Siegfried R. | Zendy

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Diversity‐Oriented Synthesis of Polycyclic Scaffolds by Modification of an Anodic Product Derived from 2,4‐Dimethylphenol

Author(s) -

Barjau Joaquin,

Schnakenburg Gregor,

Waldvogel Siegfried R.

Publication year - 2011

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.201006637

Subject(s) - chemoselectivity , anode , reactivity (psychology) , anodic oxidation , diversity (politics) , product (mathematics) , chemistry , polymer chemistry , materials science , organic chemistry , mathematics , catalysis , electrode , sociology , medicine , alternative medicine , geometry , pathology , anthropology

Like a Swiss army knife : The pentacycle shown, which results from the anodic oxidation of 2,4‐dimethylphenol, displays a wealth of potential reactivity. Depending on the applied reaction conditions a variey of polycyclic architectures are obtained with impressive stereo‐, regio‐, and chemoselectivity.

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