ChemInform Abstract: Synthesis of Atropisomeric Heterotopic S-Donor Ligands Through Asymmetrization of C2-Symmetry 2,2′-Disubstituted 1,1′-Binaphthalene Derivatives.
✍ Scribed by D. FABBRI; S. PULACCHINI; S. GLADIALI
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Synthesis of Atropisomeric Heterotopic S-Donor Ligands Through Asymmetrization of C2-Symmetry 2,2'-Disubstituted 1,1'-Binaphthalene Derivatives.
-Procedures for the conversion of the C2-symmetric binaphthol (I) into atropisomeric dithiols such as (V) or the corresponding O,S-chelating ligand (IX) are reported. Key steps are the asymmetrization of the dicarbamate (II) through selective removal of one S-carbamoyl group and the asymmetrization of the diol (I) via selective monoacylation. -(FABBRI, D.;
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An Asymmetric Synthesis of (1S,4R)-4-Amino-2-cyclopentenol Derivatives. -Chiral cyclopentenols (II), prepared from mesocyclopentene oxide (I) under optimized conditions, are easily transformed to the title compounds (III) (useful chiral synthons) by oxidation. -(ASAMI,