## Abstract For Abstract see ChemInform Abstract in Full Text.
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.
📜 SIMILAR VOLUMES
## 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