Substituent effects on oxidation-induced formation of quinone methides from arylboronic ester precursors.
about
Novel delivery approaches for cancer therapeutics.The leaving group strongly affects H₂O₂-induced DNA cross-linking by arylboronates.Self-immolative spacers: kinetic aspects, structure-property relationships, and applications.Photochemical Generation of Benzyl Cations That Selectively Cross-Link Guanine and Cytosine in DNA.Hydrogen peroxide activated quinone methide precursors with enhanced DNA cross-linking capability and cytotoxicity towards cancer cells.
P2860
Substituent effects on oxidation-induced formation of quinone methides from arylboronic ester precursors.
description
2013 nî lūn-bûn
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2013年学术文章
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2013年学术文章
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name
Substituent effects on oxidati ...... arylboronic ester precursors.
@en
Substituent effects on oxidati ...... arylboronic ester precursors.
@nl
type
label
Substituent effects on oxidati ...... arylboronic ester precursors.
@en
Substituent effects on oxidati ...... arylboronic ester precursors.
@nl
prefLabel
Substituent effects on oxidati ...... arylboronic ester precursors.
@en
Substituent effects on oxidati ...... arylboronic ester precursors.
@nl
P2093
P2860
P356
P1476
Substituent effects on oxidati ...... arylboronic ester precursors.
@en
P2093
Robin Christiansen
Xiaohua Peng
P2860
P304
P356
10.1002/CHEM.201300539
P407
P577
2013-05-13T00:00:00Z