The synthesis as well as the stereochemical characterization preparation of our compounds proved to be very satisfactory and all cyclophanes were obtained in high yield (Υ 70%). (in solution) of sterically congested cyclophanes containing the chiral spirobiindanol phosphonate moiety is reported. On
Synthesis and Clathration Properties of Novel Chiral Cyclophanes Containing Spirobiindanol Phosphonates Unit
β Scribed by Giuseppe A. Consiglio; Salvatore Failla; Paolo Finocchiaro; Fabio Marchetti
- Book ID
- 104439883
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- English
- Weight
- 285 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1472-7862
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract We describe the synthesis and properties of oligonucleotides (ONs) containing biaryl units, which are composed of a bis(hydroxymethyl)benzene residue and a naphthalene or pyrene moiety. We found that by introducing the biaryl units into the ONs, the aromatic chromophores were suitably a
## Abstract An optically active levoazobenzene polyurethane (PU) was synthesized and was based on the chromophore 4β(4β²βnitrophenylazo) phenylamine, the chiral reagent L(β)βtartaric acid, and toluene diisocyanate. The chemical structure and thermal properties were characterized by ultravioletβvisib