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he synthesis and characterization of novel optically-active macrocycles, obtained by esterification reaction from a binaphthyl-containing diol and phthalic or terephthalic acids, and possessing overall D-2 or D-3 symmetry, is described.

Rigid Optically-Active D2 and D3 Macrocycles

RICCI, MARINA;PASINI, DARIO
2003-01-01

Abstract

he synthesis and characterization of novel optically-active macrocycles, obtained by esterification reaction from a binaphthyl-containing diol and phthalic or terephthalic acids, and possessing overall D-2 or D-3 symmetry, is described.
2003
The Organic Chemistry/Polymer Science category includes resources concerned with the related fields of organic chemistry and polymer science. The organic chemistry resources deal with compounds of carbon with the exception of certain simple ones, such as the carbon oxides, carbonates, cyanides and cyanates (see Inorganic & Nuclear Chemistry). This category includes research on synthetic and natural organic compounds that may include other elements, such as hydrogen and oxygen, but also nitrogen, halogens, sulphur and phosphorous. Resources concerned with hydrocarbons, organic compounds containing only the elements carbon and hydrogen, are also included in this category. Examples are the alkanes, alkenes, alkynes and aromatics, such as benzene and naphthalene. Polymer science includes all resources dealing with the study, production and technology of polymers, which are compounds composed of very large molecules made up of repeating molecular units (monomers). Polymers may be natural substances, such as polysaccharides or proteins, or synthetic materials, such as nylon or polyethylene.
ORGANIC & BIOMOLECULAR CHEMISTRY
sì
WOS:000185547400002
2-s2.0-0142062950
Esperti anonimi
Inglese
Internazionale
STAMPA
1
19
3261
3262
2
CHIRALITY; MACROCYCLES; MOLECULAR RECOGNITION; CONFORMATIONAL DYNAMICS
2
info:eu-repo/semantics/article
262
Ricci, Marina; Pasini, Dario
1 Contributo su Rivista::1.1 Articolo in rivista
none
1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/115500
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