ChemInform Abstract: 2-Phospha[3]ferrocenophanes with Planar Chirality: Synthesis and Use in Enantioselective Organocatalytic [3 + 2] Cyclizations.
β Scribed by Arnaud Voituriez; Armen Panossian; Nicolas Fleury-Bregeot; Pascal Retailleau; Angela Marinetti
- Publisher
- John Wiley and Sons
- Year
- 2009
- Weight
- 51 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
An Organocatalytic [3 + 2] Cyclization Strategy for the Highly Enantioselective Synthesis of Spirooxindoles. -Phosphine-promoted [3 + 2] annulation reactions between electron-poor allenes and 3-arylidene indolin-2-ones afford a new organocatalytic strategy for the synthesis of the spirocyclic core o
Use of Chiral Glycerol 2,3-Carbonate in the Synthesis of 3-Aryl-2oxazolidinones. -In a search for new reversible inhibitors of monoamine oxidase related to befloxatone, the efficient synthesis of chiral N-arylated 5-methoxymethyl-2-oxazolidinones (III) via regiospecific ring-opening of commercially