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

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; in revised form: 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

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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.

AMA 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(3):1466-1472.

Chicago/Turabian Style

Sashida, Haruki; Satoh, Hirohito; Ohyanagi, Kazuo; Kaname, Mamoru. 2010. "Novel Oxidative Ring Opening Reaction of 1H-Isotelluro-chromenes to Bis(o-formylstyryl) Ditellurides." Molecules 15, no. 3: 1466-1472.

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