File:Stereoselective E-enolate formation of esters in aldol addtion reactions.svg
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Summary
| Description |
Stereoselective E-enolate formation of esters and its application in diastereoselective aldol addition reactions as reported in J. Am. Chem. Soc. (1989) 111, 3441–3442 Bulky boron compounds such as dicyclohexylchloroborane (Cy2BCl) and less sterically hindered amine bases such as triethylamine (Et3N) almost quantitatively give E-boron enolates, which in turn lead to the anti-Aldol as main product. Image generated in ChemDraw Professional 20.0 and converted into SVG file using Scribus 1.5.4 + Inkscape 1.0.1 (drawn according to official Manual of Style guidelines) |
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| Date | |||
| Source | Own work | ||
| Author | Chem Sim 2001 | ||
| Permission (Reusing this file) |
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| SVG development |  This structural formula was created with ChemDraw. |
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 21:44, 26 February 2022 | | 1,211 × 229 (38 KB) | Chem Sim 2001 | fixed enolate structure |
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