Journal ArticleDOI
Reaction of phenacyltriphenylarsonium bromide with anilines: synthesis of 2-phenylindoles through arsenic ylide
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This article is published in Tetrahedron Letters.The article was published on 1977-01-01. It has received 4 citations till now. The article focuses on the topics: Bromide & Ylide.read more
Citations
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Journal ArticleDOI
Reaction of phenacyltriphenylarsonium bromide with aromatic primary amines: synthesis of 2-arylindoles and 2-arylbenzindoles through arsenic ylide
Raj K. Bansal,Sushant Sharma +1 more
TL;DR: The reaction of phenacyltriphenylarsonium bromide with aromatic primary amines provides a good method for the synthesis of 2-arylindoles and 2 -arylbenzindoles through arsenic ylide, and a range of indole and benzindole derivatives have been prepared in good yield.
Journal ArticleDOI
Synthesis of novel methoxy and hydroxy derivatives of 2-phenyl-1H-benz[g]indoles
TL;DR: In this article, the synthesis of methoxy-derivatives of 2-phenyl-1H-benz[g]indole by condensation of α-naphthyl-amines with N-phenacyl-pyridinium salts was described.
Some reactions of arsenic ylids.
TL;DR: Para-substituted benzylidenetriarylarsoranes give olefins when the benzylidene parasubstituent is strongly electron attractive otherwise epoxides are formed as mentioned in this paper.
Journal ArticleDOI
Arsenic : Annual survey covering the years 1976 and 1977
Ralph A. Zingaro,Kurt J. Irgolic +1 more
References
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Journal ArticleDOI
Nitration of Indoles. IV. The Nitration of 2-Phenylindole1
Journal ArticleDOI
Chemistry of ylides. XX. Triphenylarsoniumphenacylide
Journal ArticleDOI
Studies on ylides: Carbonyl olefination with (p-nitro benzylidene)triphenylarsenane☆
TL;DR: In this article, a semistabilized arsonium ylide has been prepared and reacted with carbonyl compounds to yield olefins as opposed to epoxidation products.
Journal ArticleDOI
Some reactions of arsenic ylides
S. Trippett,Margaret A. Walker +1 more
TL;DR: Para-substituted benzylidenetriarylarsoranes give olefins when the benzylidene parasubstituent is strongly electron attractive otherwise epoxides are formed as discussed by the authors.
Some reactions of arsenic ylids.
TL;DR: Para-substituted benzylidenetriarylarsoranes give olefins when the benzylidene parasubstituent is strongly electron attractive otherwise epoxides are formed as mentioned in this paper.
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