62396-48-9Relevant articles and documents
Morphological control of self-assembled multivalent (SAMul) heparin binding in highly competitive media
Rodrigo, Ana C.,Bromfield, Stephen M.,Laurini, Erik,Posocco, Paola,Pricl, Sabrina,Smith, David K.
supporting information, p. 6335 - 6338 (2017/07/11)
Tuning molecular structures of self-assembling multivalent (SAMul) dendritic cationic lipopeptides controls the self-assembled morphology. In buffer, spherical micelles formed by higher generation systems bind polyanionic heparin better than worm-like micelles formed by lower generation systems. In human serum, the binding of spherical micelles to heparin is adversely affected, while worm-like micelles maintain their relative binding ability.
HYDROLYSE ENANTIOSELECTIVE D'ESTERS D'AMINOACIDE CATALYSEE PAR L'IMIDAZOLE DANS DES MICELLES INVERSES CHIRALES.1300
Andriamanampisoa, R.,Boyer, B.,Lamity, G.,Roque, J. P.
, p. 77 - 84 (2007/10/02)
This paper reports the study of the imidazole catalyzed hydrolysis of enantiomeric pairs of three aminoacid esters in reversed micelles prepared from water, heptane and a combination of both racemic or chiral surfactants and of both racemic or chiral (S)2-octanol as cosurfactants.The enantioselectivity observed is important in the combination of chiral surfactant with racemic cosurfactant, and small in the combination of racemic surfactant with chiral cosurfactant, when ω = 20 (ω = / ).This enantioselectivity is also affected by the nature of the cosurfactant, the size of micelles and the nature of the substrate.The results prove that the reaction occurs effectively in a chiral microenvironment, the micelle membrane, and indicate that the cosurfactant is actually present in this membrane.
