Convenient synthesis of alkynyl aryl seleno- and telluro-ethers

Darren J. Cook; Anthony F. Hill; D. James Wilson

doi:10.1039/a708647d

Convenient synthesis of alkynyl aryl seleno- and telluro-ethers

Darren J. Cook, Anthony F. Hill^*, D. James Wilson

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

24 Citations (Scopus)

Abstract

The reaction of bis(alkynyl)mercurials [Hg(C≡CR)₂] (R = C₆H₅, C₆H₄Me-4 or ferrocenyl) with diaryl dichalcogenides (ER′)₂ (E = Se, R′ = C₆H₅ or C₆H₄Cl-4; E = Te, R′ = C₆H₅) conveniently provided high yields of the alkynyl aryl chalcogenoethers RC≡CER′.

Original language	English
Pages (from-to)	1171-1173
Number of pages	3
Journal	Journal of the Chemical Society - Dalton Transactions
Issue number	7
DOIs	https://doi.org/10.1039/a708647d
Publication status	Published - 7 Apr 1998
Externally published	Yes

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title = "Convenient synthesis of alkynyl aryl seleno- and telluro-ethers",

abstract = "The reaction of bis(alkynyl)mercurials [Hg(C≡CR)2] (R = C6H5, C6H4Me-4 or ferrocenyl) with diaryl dichalcogenides (ER′)2 (E = Se, R′ = C6H5 or C6H4Cl-4; E = Te, R′ = C6H5) conveniently provided high yields of the alkynyl aryl chalcogenoethers RC≡CER′.",

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year = "1998",

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AU - Wilson, D. James

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N2 - The reaction of bis(alkynyl)mercurials [Hg(C≡CR)2] (R = C6H5, C6H4Me-4 or ferrocenyl) with diaryl dichalcogenides (ER′)2 (E = Se, R′ = C6H5 or C6H4Cl-4; E = Te, R′ = C6H5) conveniently provided high yields of the alkynyl aryl chalcogenoethers RC≡CER′.

AB - The reaction of bis(alkynyl)mercurials [Hg(C≡CR)2] (R = C6H5, C6H4Me-4 or ferrocenyl) with diaryl dichalcogenides (ER′)2 (E = Se, R′ = C6H5 or C6H4Cl-4; E = Te, R′ = C6H5) conveniently provided high yields of the alkynyl aryl chalcogenoethers RC≡CER′.

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Convenient synthesis of alkynyl aryl seleno- and telluro-ethers

Abstract

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