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Lutein diacetate

Zsila, F., Z. Bikadi, Z. Keresztes, J. Deli, and M. Simonyi. 2001b. Investigation of the self-organization of lutein diacetate by electronic absorption, circular dichroism spectroscopy, and atomic force microscopy. J. Phys. Chem. B 105 9413-9421. [Pg.157]

Fig. 116. Layer polyamide (perlon)-cellulose (80 + 20) solvent petrol ether (BP 100—120° C)-butanone-methanol (78 + 11 + 11). Substances a eschscholtz-xanthin b capsorubin c capsanthin (in 1) zeaxanthin d (in 2 and 3) fucoxanthin e lutein / fucoxanthin acetate g lutein monoacetate h cryptoxanthin i by-product from acetylation oi f k lutein diacetate. Applied ia + c + d + 26+c + d 9 + A 36 + c + d + e+ / + [42]... Fig. 116. Layer polyamide (perlon)-cellulose (80 + 20) solvent petrol ether (BP 100—120° C)-butanone-methanol (78 + 11 + 11). Substances a eschscholtz-xanthin b capsorubin c capsanthin (in 1) zeaxanthin d (in 2 and 3) fucoxanthin e lutein / fucoxanthin acetate g lutein monoacetate h cryptoxanthin i by-product from acetylation oi f k lutein diacetate. Applied ia + c + d + 26+c + d 9 + A 36 + c + d + e+ / + [42]...
LUTEINIZING HORMONE-RELEASING HORMONE, DIACETATE TETRAHYDRATE... [Pg.131]

Lutein (14), as diacetate, upon epoxidation with w-chlorperbenzoic acid gave a minor epoxide identical with lutein epoxide (46) diacetate besides the major 3,5-cis epoxide (46). In a similar way zeaxanthin (26) diacetate had previously been converted to violaxanthin (32) diacetate (20), the 3,5- and 3, 5 -Irons compounds being obtained as minor products in addition to the major 3,5- and 3, 5 -cis derivatives, consistent with results for simple model compounds (20) and subsequent NMR data (78). [Pg.141]


See other pages where Lutein diacetate is mentioned: [Pg.148]    [Pg.140]    [Pg.148]    [Pg.140]    [Pg.111]    [Pg.332]    [Pg.256]   
See also in sourсe #XX -- [ Pg.141 ]




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