Oxidative Cyclization Reaction of 2‐Aryl‐Substituted Cinnamates To Form Phenanthrene Carboxylates by Using MoCl 5 | Zendy

Wehming Kathrin | Zendy; Schubert Moritz | Zendy; Schnakenburg Gregor | Zendy; Waldvogel Siegfried R. | Zendy

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Oxidative Cyclization Reaction of 2‐Aryl‐Substituted Cinnamates To Form Phenanthrene Carboxylates by Using MoCl 5

Author(s) -

Wehming Kathrin,

Schubert Moritz,

Schnakenburg Gregor,

Waldvogel Siegfried R.

Publication year - 2014

Publication title -

chemistry – a european journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.687

H-Index - 242

eISSN - 1521-3765

pISSN - 0947-6539

DOI - 10.1002/chem.201404510

Subject(s) - cinnamates , phenanthrene , aryl , reagent , chemistry , oxidative phosphorylation , oxidative coupling of methane , organic chemistry , medicinal chemistry , photochemistry , polymer chemistry , catalysis , biochemistry , alkyl

Invited for the cover of this issue is Siegfried R. Waldvogel and co‐workers at Mainz University and Bonn University. The image depicts MoCl 5 as an inexpensive, but powerful and fast‐reacting reagent for the oxidative coupling of aryls. Read the full text of the article at 10.1002/chem.201403442 .

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