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File:Stereoselective Z-enolate formation of esters in aldol addtion reactions.svg
From WikiMD.com - Food, Medicine & Wellness Encyclopedia

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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 17:59, 1 March 2022 | ![]() | 1,557 × 236 (51 KB) | Chem Sim 2001 | == {{int:filedesc}} == {{Information | Description = Stereoselective ''Z''-enolate formation of esters and its application in diastereoselective aldol addition reactions as reported in [https://doi.org/10.1021/ja00191a058 ''J. Am. Chem. Soc.'' (1989) '''111''', 3441–3442] Boron compounds such as 9-chloro-9-borabicyclo[3.3.1]nonane (''B''–Cl–9–BBN) and sterically hindered amine bases such as diisopropylethylamine (''i''-Pr... |
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