Stereoselective formation of 1, 2-diiodoalkenes and their application in the stereoselective synthesis of highly functionalised alkenes via Suzuki and Stille coupling …
N Hénaff, A Whiting
Index: Henaff, Nadine; Whiting, Andrew Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 3 p. 395 - 400
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Citation Number: 22
Abstract
Treatment of an alkyne with iodine monochloride and sodium iodide at room temperature results in the formation of the thermodynamic (E [])-diiodoalkene. The corresponding (Z [])- diiodoalkene can also be produced, by treatment of the alkyne with iodine monochloride at− 78° C in the presence of tetraethylammonium iodide.
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