6533b825fe1ef96bd128309c
RESEARCH PRODUCT
Pertosylated polyaza[n](9,10)anthracenophanes
Belén AltavaM. Carmen MuñozBeatriu EscuderEnrique García-españaM. Isabel BurgueteSantiago V. Luissubject
StereochemistryOrganic Chemistrychemistry.chemical_elementReduced mobilityCrystal structureBiochemistryNitrogenchemistry.chemical_compoundCrystallographychemistryChain (algebraic topology)Drug DiscoveryAromatic moietyDerivative (chemistry)description
Abstract Pertosylated polyaza[n](9,10)antracenophanes have been obtained in high yields by a modification of the Richman-Atkins methodology. Molecular Mechanics calculations as well as the crystal structure of the N,N′,N″,N‴-Tetratosyl-2,6,9,13-tetraaza[14](9,10)anthracenophane 4 derivative reveal the existence of a well defined cavity where both the aromatic moiety and the nitrogen donor atoms converge. Reduced mobility of the aliphatic chain is also observed as well as the presence of some strain at the benzylic positions.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 1997-02-01 | Tetrahedron |