Interfacial adsorption and micellization behaviour of alkaloid based chiral compounds in aqueous medium was written by Maiti, Kajari;Prasad, Madhumita;Chatterjee, Amrita;Bhattacharya, P. K.;Moulik, S. P.. And the article was included in Journal of Surface Science and Technology in 2004.Application In Synthesis of (1S,2R,4S,5R)-1-Benzyl-2-(hydroxy(quinolin-4-yl)methyl)-5-vinylquinuclidin-1-ium chloride This article mentions the following:
Chiral compounds I, II, III and IV were synthesized and characterized. Their interfacial (at air/solution interface) adsorption and self-association in aqueous medium were studied by tensiometric, conductometric and spectrophotometric methods. The compounds formed micelles in solution with low CMC values. The results were analyzed and thermodn. of the micellization of the chiral compounds and their adsorption at the air/solution interface were evaluated and discussed. In the experiment, the researchers used many compounds, for example, (1S,2R,4S,5R)-1-Benzyl-2-(hydroxy(quinolin-4-yl)methyl)-5-vinylquinuclidin-1-ium chloride (cas: 69221-14-3Application In Synthesis of (1S,2R,4S,5R)-1-Benzyl-2-(hydroxy(quinolin-4-yl)methyl)-5-vinylquinuclidin-1-ium chloride).
(1S,2R,4S,5R)-1-Benzyl-2-(hydroxy(quinolin-4-yl)methyl)-5-vinylquinuclidin-1-ium chloride (cas: 69221-14-3) belongs to quinuclidine derivatives. Quinuclidine acts as a catalyst, a chemical building block and is used in organic synthesis. The reactions of quinuclidine compounds that lead to opening of the 1-azabi-cyclic system at the N-C and C-C bonds to give piperidine derivatives or, via subsequent rearrangements, derivatives of other heterocyclic systems, are correlated.Application In Synthesis of (1S,2R,4S,5R)-1-Benzyl-2-(hydroxy(quinolin-4-yl)methyl)-5-vinylquinuclidin-1-ium chloride
Referemce:
Quinuclidine – Wikipedia,
Quinuclidine | C7H13N | ChemSpider