Synthesis and 125Te NMR spectroscopy of α-tellurocarbonyl compounds and derivatives

Article abstract of DOI:10.1080/00397919108019802

The reaction of lithium alkyl-, alkenyl-, alkynyl-, and aryl tellurolates with α-bromocarbonyl compounds in anhydrous tetrahydrofuran gives the title compounds in yields ranging from 55-92%. The ¹²⁵Te NMR chemical shift range for these compound

Full text of DOI:10.1080/00397919108019802

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Synthetic Communications: An
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Synthesis and 125Te
NMR Spectroscopy of α-
Tellurocarbonyl Compounds
and Derivatives
Louis A. Silks III a , Jerome D. Odom b & R. Bruce
Dunlap b
a Los Alamos National Laboratory, NIH National
Stable Isotopes Resource, INC-4 , MS C-345, Los
Alamos, N. M., 87545
b Department of Chemistry , University of South
Carolina , Columbia, S. C., 29208
Published online: 23 Sep 2006.
To cite this article: Louis A. Silks III , Jerome D. Odom & R. Bruce Dunlap
(1991) Synthesis and 125Te NMR Spectroscopy of α-Tellurocarbonyl Compounds
and Derivatives, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 21:8-9, 1105-1119, DOI:
10.1080/00397919108019802
To link to this article: http://dx.doi.org/10.1080/00397919108019802
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