Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Magdolna Háda"'
Publikováno v:
Molecules, Vol 17, Iss 5, Pp 5003-5012 (2012)
Carotenoids are substantially hydrophobic antioxidants. Hydrophobicity is this context is rather a disadvantage, because their utilization in medicine as antioxidants or in food chemistry as colorants would require some water dispersibility for their
Externí odkaz:
https://doaj.org/article/0f14cd15160b4a498a020d6e1451da3e
Publikováno v:
Helvetica Chimica Acta. 93:1149-1155
For the evaluation of the synthesis of dendritic esters from carotenoids, various carotenols or their succinates were reacted with bi- and trifunctional aromatic acids and alcohols. Several methods were tested, from which the Steglich esterification
Publikováno v:
Tetrahedron Letters. 53:2480-2482
We describe the synthesis of carotenoid derivatives via the azide–alkyne click reaction and optimize the conditions for these sensitive molecules. After finding the mildest conditions possible for the reaction we were able to use the click reaction
Publikováno v:
Tetrahedron Letters. 52:3195-3197
Carotenoid–PEG esters and diesters were synthesized from several carotenols with polyethyleneglycols of different chain length to enhance the water solubility and bioavailability of these hydrophobic carotenoids. The water solubility of the product
Publikováno v:
Tetrahedron Letters. 49:3524-3526
For the evaluation of the synthesis of dendritic esters from carotenoids the C20 apocarotenoid retinol was chosen for model studies, being a commercially available hydroxy carotenoid. Dimers were synthesized from retinol with dicarboxyl cores and fro
Publikováno v:
Helvetica Chimica Acta; Jun2010, Vol. 93 Issue 6, p1149-1155, 7p
Publikováno v:
Molecules. May2012, Vol. 17 Issue 5, p5003-5012. 10p. 6 Diagrams.