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On the use of deuterium isotope effects in chemical synthesis

✍ Scribed by Gregory B Dudley; Samuel J Danishefsky; George Sukenick


Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
80 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


The decreased kinetic acidity of deuterium relative to hydrogen can be used to gain an advantage in the reductive cyclization of an alkenyllithium species onto a ketone. The intermediate alkenyllithium can add to the carbonyl or abstract an a-proton, giving rise to two products. The yield of the cyclized product can be increased, and the formation of the uncyclized by-product can be suppressed, by replacing the acidic protons with deuterons prior to cyclization.


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