## Abstract Aromatic as well as aliphatic aldehydes undergo the Henry reaction with nitromethane under catalysis of an in situ generated chiral amino alcohol—Zn complex to give the corresponding β‐nitroalcohols in moderate to good enantioselectivity.
ChemInform Abstract: Asymmetric syn-Selective Henry Reaction Catalyzed by the Sulfonyldiamine—CuCl—Pyridine System.
✍ Scribed by Takayoshi Arai; Ryuta Takashita; Yoko Endo; Masahiko Watanabe; Akira Yanagisawa
- Publisher
- John Wiley and Sons
- Year
- 2008
- Weight
- 49 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
## Abstract A variety of amino acid‐derived water‐soluble primary‐tertiary diamines is prepared and successfully applied as organocatalyst in the aldol reaction of protected hydroxyacetone derivatives (I) and (IV) with aromatic aldehydes.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
1997 carboxylic acid esters carboxylic acid esters (benzene compounds) Q 0530 35 -098 Enantioselective Acyclic Stereoselection under Catalyst Control. Part 2. Asymmetric Synthesis of syn-and anti-1,3-Diols Incorporating an Acetate Equivalent by the Chiral Oxazaborolidinone-Catalyzed Aldol Reaction.