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Enantioselective addition of chirally modified allylboranes to N-(trimethylsilyl)benzaldehyde imine

✍ Scribed by Katsuhiro Watanabe; Koichi Ito; Shinichi Itsuno


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
200 KB
Volume
6
Category
Article
ISSN
0957-4166

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πŸ“œ SIMILAR VOLUMES


ChemInform Abstract: Enantioselective Sy
✍ Shinichi Itsuno; Katsuhiro Watanabe; Takeshi Matsumoto; Shizue Kuroda; Ayako Yok πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 36 KB πŸ‘ 2 views

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

ChemInform Abstract: Enantioselective Al
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1997 stereochemistry stereochemistry (general, optical resolution) O 0030 ## 43 -041 Enantioselective Allylation of N-(Trimethylsilyl)benzaldehyde Imine Using Polymer-Supported Chiral Allylboron Reagents. -Both polymers (I) and (II) are found to be excellent chiral ligands in the title reactions.