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Molecules 2010, 15(3), 1466-1472; doi:10.3390/molecules15031466

Novel Oxidative Ring Opening Reaction of 1H-Isotelluro-chromenes to Bis(o-formylstyryl) Ditellurides

1
Faculty of Pharmaceutical Sciences, Hokuriku University, Kanagawa-machi, Kanazawa 920-1181, Japan
2
Faculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan
*
Author to whom correspondence should be addressed.
Received: 5 January 2010 / Revised: 2 February 2010 / Accepted: 5 March 2010 / Published: 9 March 2010
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Abstract

The oxidation of 1-unsubstituted or 1-phenyl-1H-isotellurochromenes with m-chloroperbenzoic acid (mCPBA) in CHCl3 resulted in a ring opening reaction to produce as the sole products the corresponding o-formyl or benzoyl distyryl ditellurides, which were also produced by the hydrolysis of the 2-benzotelluropyrylium salts readily prepared from the parent isotellurochromene.
Keywords: isotellurochromene; mCPBA oxidation; 2-benzotelluropyrylium salt; distyryl ditelluride isotellurochromene; mCPBA oxidation; 2-benzotelluropyrylium salt; distyryl ditelluride
This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0).

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MDPI and ACS Style

Sashida, H.; Satoh, H.; Ohyanagi, K.; Kaname, M. Novel Oxidative Ring Opening Reaction of 1H-Isotelluro-chromenes to Bis(o-formylstyryl) Ditellurides. Molecules 2010, 15, 1466-1472.

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