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・ Indium tin oxide
・ Indium trihydride
・ Indium wire
・ Indium(I) bromide
・ Indium(III) bromide
・ Indium(III) chloride
・ Indium(III) fluoride
・ Indium(III) hydroxide
・ Indium(III) oxide
・ Indium(III) selenide
・ Indium(III) sulfate
・ Indium(III) sulfide
・ Indium(III) telluride
・ Indium-111
・ Indium-111 WBC scan
Indium-mediated allylation
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Indium-mediated allylation : ウィキペディア英語版
Indium-mediated allylation

Indium-Mediated Allylations (IMAs) are important chemical reactions for the formation of carbon–carbon bonds. This reaction has two steps: first, indium inserts itself between the carbon–halogen bond of an allyl halide, becoming the organoindium intermediate; second, this allyl indide intermediate reacts with an electrophile to synthesize one of a wide range of compounds, such as carbohydrates and antihelminthic drugs. This reaction is depicted in the scheme below:


Although this reaction occurs in two steps, it is commonly done as a Barbier reaction where the indium, allyl halide, and electrophile are all mixed together in a one-pot process.
Indium reacts more readily than other metals, such as Mg, Pb, Bi, or Zn and does not require a promoter or flammable organic solvent to drive the reaction. IMAs have advantages over other carbon bond forming reactions because of their ability to be carried out in water, which is cheap and environmentally friendly. Therefore, these reactions represent Green chemistry, providing a safer alternative to the very common Grignard reaction, performed with Mg. Reactions yield high stereo- and regio-selectivity with few by-products making it easy to purify the desired product.
==Industrial use==

The ability of the IMA reaction to form new carbon–carbon bonds allows simple molecules found in petroleum to be built into bigger, more complex molecules like drugs. Indium metal is very good at selectively synthesizing specific products.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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