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A: When you are using a tool like sondtool, you are interested in the output generated by it. Thus, you have to check the output of sondtool to make sure it’s the output you are expecting. Friedrich Wilhelm von Wiese Friedrich Wilhelm von Wiese (or von Wes) (died 5 December 1736) was a German statesman in Poland, Germany and Great Britain. Life After having been active as a diplomat from 1691 to 1697, he became Prussian envoy to Poland in 1699. He was well received and became chancellor of the crown prince Frederick IV. In this position he engaged in successfully dealing with the Russo-Swedish War of 1708-1714. Wiese was elected a member of the Board of War in 1710. After the election of Stanisław Leszczyński as King of Poland, Wiese supported him in opposing the manoeuvres of the Great Elector. This was achieved when the Great Elector appointed Wiese ambassador to England. In 1714 the Saxon Wars were threatening to trigger a war with Great Britain. As a German prince, Wiese would not have been able to take up this post. Wiese’s career was however on a trajectory to Great Britain, where he was appointed as a diplomat, but was not a Knight of the Order of the Garter. He died in London at the age of 52. See also Polish embassy to the United Kingdom References External links Friedrich Wilhelm von Wiese Category:1736 deaths Category:German diplomats Category:Year of birth unknownExtraction and Epoxidation of Dibenzo-Fused Biaryls: Formation of a Hybrid Polycyclic Skeleton by Ene and Ring Expansions. The synthesis of highly stable, electron deficient heterocycles is of importance for the development of novel organic electronic devices. Herein, we report an original synthetic route toward dibenzo-fused biaryls. An efficient approach, based on an elegant oxidative [1,2-dicarbonyl]-2-phenylcyclopropyl metalation-ring expansion protocol, allowed for the construction of a variety of electron-deficient dibenzo-fused biaryls. The resulting 1,1-diaryloxonium ylides were subjected to epoxidation to give, in excellent yields, the corresponding epoxides, which were then subjected to reactions leading to the formation of novel polycyclic compounds, including 3,5-bis(diphenylphosphinothiomethyl)-2,2′-bipyridine (PDPT). X-ray crystallography confirmed the formation of the target heterocyclic compounds.

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