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The stereochemical outcome of the Mitsunobu reactions of para-oxygenated benzylic alcohols

✍ Scribed by Roger F.C. Brown; W.Roy Jackson; Tom D. McCarthy


Book ID
108379978
Publisher
Elsevier Science
Year
1993
Tongue
French
Weight
135 KB
Volume
34
Category
Article
ISSN
0040-4039

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Complex stereochemical course of the mit
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## The Mitsunobu esterificafion reaction of dicycZopentadienoZs yields mixtures of inversion and retention products. Deuteriwn iabeling demonstrates variable levels of aZZyZic rearrangement. The Mitsunobu esterification procedure has recently become a very important and useful tool in 1 organic sy