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1,8-naphthalenediol

 
National Institutes of Health

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2020
2020
The 1,8-naphthalenediolate [1,8-O2C10H8] supported boronic and boric acid esters of general formula X-B(1,8-O2C10H8), where X… Expand
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2018
2018
1,8-Naphthalenediol (dihydroxynaphthalene, 1,8-DHN) has been shown to be a potent hydrogen atom transfer (HAT) antioxidant… Expand
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2018
2018
The hydrogen bond donating ability of 1,8-naphthalenediol was investigated via a series of 1 " role="presentation"> 1 1 ^{1} H… Expand
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2017
2017
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… Expand
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2015
2015
The mechanism of the cytotoxic function of cisplatin and related anticancer drugs is based on their binding to the nucleobases of… Expand
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2009
2009
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… Expand
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2006
2006
The heterodinuclear complex [LCuIIVIVO] 1 was synthesized by using a new unsymmetric dinucleating ligand based on 1,8… Expand
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2005
2005
A facile synthesis of 2-formyl-1,8-naphthalenediol is reported. Its potential as a general precursor for the preparation of… Expand
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2003
2003
Abstract The structure of the intensely coloured red product obtained through the reaction of 1,8-naphthalenediol with 1,1… Expand
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1981
1981
Propranolol (Inderal; 1) is extensively metabolized in man. Metabolites of interest pharmacologically include ring-hydroxylated… Expand
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