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- W2015446548 abstract "Photoirradiation of solutions of natural (4Z,15Z)-biliru-bin-IXα in chloroform with ˜366 nm UV light leads rapidly to a new photoisomer that has been characterized by NMR spectroscopy and by its (ground-state reaction) adducts with methanol and other protic nucleophiles. Unlike the previously described Z →E geometric isomeri-zation important in phototherapy of neonatal jaundice, the new photoisomerization involves regiospecific pho-toautomerization to afford 2-ethenyl-18-ethylidene-l,10,19,22,24-pentahydro-2,7,13,17-tetramethyl-l,19-dioxo-21H-biline-8,12-dipropanoic acid." @default.
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- W2015446548 date "1999-12-01" @default.
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- W2015446548 title "A New Photoisomerization of Bilirubin" @default.
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- W2015446548 doi "https://doi.org/10.1111/j.1751-1097.1999.tb08306.x" @default.
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