A mechanistic model for the enantioselective addition of diethylzinc to benzaldehyde with chiral tridentate lithium complexes as catalysts correctly predicts the observed direction of enantioselectivity which occurs at levels of 8595% ee. A recent paper from these laboratories described two rationa
โฆ LIBER โฆ
Zinc complexes of chiral phenols as catalysts for enantioselective addition of organozinc reagents to aldehydes
โ Scribed by E.J Corey; Francis J Hannon
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 240 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
A class of zinc (II) chelates with chiral tertiary amino phenolic alcohols serve as effective catalysts for the enantioselective addition of diethylzinc to aromatic aldehydes with predictable absolute stereochemistry.
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