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- W2952568765 abstract "The novel enediynes 7–9 are synthesized from xylitol 1via the keto-enediyne 2; they are aromatized by 1,8-diazabicyclo[5.4.0]undec-7-ene in cyclohexa-1,4-diene–benzene through a radical pathway and by diethylamine in Me2SO–tris-HCl, pH 8.5 buffer through a polar pathway, and exhibit gunine-selective DNA cleavage under basic conditions with no additive." @default.
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- W2952568765 date "2010-08-18" @default.
- W2952568765 modified "2023-09-23" @default.
- W2952568765 title "ChemInform Abstract: Design, Cycloaromatization and Guanine-Selective DNA Cleavage of Novel Enediynes." @default.
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- W2952568765 doi "https://doi.org/10.1002/chin.199511258" @default.
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