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Synlett 2003(11): 1725-1727
DOI: 10.1055/s-2003-41006
DOI: 10.1055/s-2003-41006
LETTER
© Georg ThiemeVerlag Stuttgart ˙ New York
Indium(I) Iodide-Mediated Chemo-,Regio-, and Stereoselective Hydrotelluration of 2-Alkyn-1-olDerivatives
Further Information
Received
18 March 2003
Publication Date:
13 August 2003 (online)
Publication History
Publication Date:
13 August 2003 (online)
Abstract
Indium(I) iodide promotes the rigorous chemo-, regio-, and stereoselectivehydrotelluration of 2-alkyn-1-ol derivatives with diphenylditelluride.The Markovnikov adducts with stereochemistry corresponding to an anti addition of the tellurol constituentsacross the triple bond were obtained in good yields.
Key words
indium(I) iodide - vinylic tellurides - hydrotelluration - Markovnikov addition - stereoselectivity
- 1
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References
Compound 1 ishighly air-sensitive, and decomposes producing the correspondingditelluride. We have not attempted to isolate it, and its formationis based on the analogous production of IIn(EC6H5)2,E = S, Se. [6]