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Stereoselective aldol condensation of boron enolates to trans α,β-epoxy aldehydes

✍ Scribed by Giuliana Righi; Francesca Spirito; Carlo Bonini


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

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✦ Synopsis


A study on the addition of boron enolates of methyl ketones to trans a,b-epoxy aldehydes is reported. The reaction proceeds with an excellent anti stereoselectivity, consistent with the Felkin-Ahn model, toward the synthesis of hydroxylated compounds with defined stereochemistry.


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Regiospecific Acylation, Alkylation, and
✍ Ferdinand Näf; René Decorzant 📂 Article 📅 1974 🏛 John Wiley and Sons 🌐 German ⚖ 709 KB

## Abstract The magnesium 3,3‐dimethylcyclohex‐1‐enolate **1i**, formed in the copper catalyzed addition of methylmagnesium iodide to 3‐methylcyclohex‐2‐enone, has been subjected to regiospecific electrophilic reactions such as acylation, alkylation, and aldol condensation in order to find a new ac