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1,2-Benzoquinones

Known as: o-Benzoquinones 
 
National Institutes of Health

Papers overview

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2016
2016
Oxidation of polyphenols to quinones serves as an antioxidative mechanism, but the resulting quinones may induce damage to… Expand
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Highly Cited
2016
Highly Cited
2016
Arynes are highly reactive intermediates having several applications in organic synthesis for the construction of various ortho… Expand
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2015
2015
Quantum phase transition achieved by fine tuning the continuous phase transition down to zero kelvin is a challenge for solid… Expand
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Highly Cited
2005
Highly Cited
2005
[reaction: see text] The zwitterionic intermediate generated from dialkyl azodicarboxylate and triphenylphosphine on reaction… Expand
Highly Cited
2001
Highly Cited
2001
Variation of the ferroelectric phase transition has been investigated for a series of isomorphous donor (D)-acceptor (A) charge… Expand
Highly Cited
1999
Highly Cited
1999
One-electron reduction of quinones (Q) by ascorbate (AscH ); (1) AscH + Q --> Q*- + Asc*- + H+, followed by the oxidation of… Expand
1993
1993
A series of 4,5-diamino-substituted-1,2-benzoquinones were prepared from catechol and the corresponding secondary amines in high… Expand
1989
1989
Abstract Lignin and lignin-related compounds were oxidized with potassium nitrosodisulfonate, hydrogen peroxide, and peracetic… Expand
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1987
1987
The properties of the semiquinone radicals produced for 2,5-bis(carboethoxyamino)-3,6-diaziridinyl-1,4-benzoquinone (AZQ) and 2,5… Expand
Highly Cited
1983
Highly Cited
1983
Standard midpoint potentials have been determined for p-benzoquinone, methoxy-p-benzoquinone and 2,3-, 2,5-, and 2,6-dimethoxy-p… Expand
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