Reactions of tris(2-pyridyl)phosphine oxides with electrophiles: Formation of 5-substituted 2,2′-bipyridyls
✍ Scribed by Yuzuru Uchida; Masami Matsumoto; Haruyasu Kawamura
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 146 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.10085
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✦ Synopsis
Abstract
The reaction of tris(2‐pyridyl)phosphine oxides with benzeneselenenyl chloride in methanol gave the corresponding 5‐phenylseleno‐2,2′‐bipyridyls together with a small amount of 2,2′‐bipyridyls. Similarly, the reaction with arenesulfenyl chlorides in aqueous acetonitrile afforded two kinds of coupling products, 5‐phenylthio‐2,2′‐bipyridyls and 2,2′‐bipyridyls. While in the reaction with arenesulfinyl chlorides in aqueous acetonitrile, four corresponding bipyridyl derivatives, 2,2′‐bipyridyls, 5‐arylthio‐2,2′‐bipyridyls, 5‐arylsulfinyl‐2,2′‐bipyridyls, and 5‐arylsulfonyl‐2,2′‐bipyridyls, were formed. © 2003 Wiley Periodicals, Inc. Heteroatom Chem 14:72–81, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.10085
📜 SIMILAR VOLUMES
Treatment of tris(2-pyridyl)phosphine or tris(2-pyridyl)phosphine oxide with electrophiles such as chlorine, bromine, deuterium chloride, or benzenediazonium chloride gave unusual coupling products, i.e., 5-chloro-, 5-bromo-, 5-deuterio-, or 5-phenylazo-2,2Јbipyridyls, respectively, as a major coupl
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