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Novel strategy of using a C2 symmetric chiral diether in the enantioselective conjugate addition of an organolithium to an .alpha.,.beta.-unsaturated aldimine

โœ Scribed by Tomioka, Kiyoshi; Shindo, Mitsuru; Koga, Kenji


Book ID
121339622
Publisher
American Chemical Society
Year
1989
Tongue
English
Weight
896 KB
Volume
111
Category
Article
ISSN
0002-7863

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ChemInform Abstract: Design, Synthesis,
โœ Mitsuru Shindo; Kenji Koga; Kiyoshi Tomioka ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons โš– 39 KB ๐Ÿ‘ 2 views

Design, Synthesis, and Application of a C 2 Symmetric Chiral Ligand for Enantioselective Conjugate Addition of Organolithium to ฮฑ,ฮฒ-Unsaturated Aldimine. -Acyclic aldimines (I), cyclic aldimines (IV), and naphthaldehyde imines like (VI) undergo enantioselective conjugate additions to organolithiums