1,8-naphthalenediol
National Institutes of Health
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The 1,8-naphthalenediolate [1,8-O2C10H8] supported boronic and boric acid esters of general formula X-B(1,8-O2C10H8), where X…
1,8-Naphthalenediol (dihydroxynaphthalene, 1,8-DHN) has been shown to be a potent hydrogen atom transfer (HAT) antioxidant…
The hydrogen bond donating ability of 1,8-naphthalenediol was investigated via a series of 1 " role="presentation"> 1 1 ^{1} H…
Two new dysprosium complexes, [Dy(H5L)(NO3)2(CH3OH)2]·4CH3OH (1) and [Dy2(H5L)2(NO3)4(H2O)2]·10CH3OH (2), were isolated from the…
The mechanism of the cytotoxic function of cisplatin and related anticancer drugs is based on their binding to the nucleobases of…
In mammals, aging is linked to a decline in the activity of citrate synthase (CS; E.C. 2.3.3.1), the first enzyme of the citric…
The extension of Robson-type ligands from dinucleating based on 2,6-diformylphenol to trinucleating based on 2,7-diformyl-1,8…
The heterodinuclear complex [LCuIIVIVO] 1 was synthesized by using a new unsymmetric dinucleating ligand based on 1,8…
A facile synthesis of 2-formyl-1,8-naphthalenediol is reported. Its potential as a general precursor for the preparation of…
Propranolol (Inderal; 1) is extensively metabolized in man. Metabolites of interest pharmacologically include ring-hydroxylated…