Enantioselective Synthesis of Optically Active Homoallylamines by Nucleophilic Addition of Chirally Modified Allylboranes to N-Silylimines. -A variety of chirally modified allylboron reagents, readily generated from the corresponding chiral bidentate ligands and triallylborane in the presence of Et
โฆ LIBER โฆ
ChemInform Abstract: Enantioselective Synthesis of Optically Active Homoallylamines by Allylboration of N-Diisobutylaluminum Imines.
โ Scribed by Katsuhiro Watanabe; Shizue Kuroda; Ayako Yokoi; Koichi Ito; Shinichi Itsuno
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
Enantioselective Synthesis of Optically Active Homoallylamines by Allylboration of N-Diisobutylaluminum Imines.
-A convenient synthesis of optically active homoallylamines (III) and (VI) is presented. It involves the enantioselective allylboration of title aluminum imines (I) and (V), resp., with chirally modified allylboron reagents like (II) or (IV). -
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