| 1 |
Synthesis of an oligodeoxyribonucleotide adduct of mitomycin C by the postoligomerization method via a triamino mitosene
Champeil E, Paz MM, Ladwa S, Clement CC, Zatorski A, Tomasz M
Journal of the American Chemical Society, 130(29), 9556, 2008 |
| 2 |
Hydrogen-bond acid/base catalysis: A density functional theory study of protonated guanine-(substituted) cytosine base pairs as models for nucleophilic attack on mitomycin in DNA
Dannenberg JJ, Tomasz M
Journal of the American Chemical Society, 122(9), 2062, 2000 |
| 3 |
The purine-2-amino group as the critical recognition element for sequence-specific alkylation and cross-linking of DNA by mitomycin C (vol 120, pg 11581, 1998)
Tomasz M, Das A, Tang KS, Ford MGJ, Minnock A, Musser SM, Waring MJ
Journal of the American Chemical Society, 121(5), 1112, 1999 |
| 4 |
The purine 2-amino group as the critical recognition element for sequence-specific alkylation and cross-linking of DNA by mitomycin C
Tomasz M, Das A, Tang KS, Ford MGJ, Minnock A, Musser SM, Waring MJ
Journal of the American Chemical Society, 120(45), 11581, 1998 |
| 5 |
2,7-Diaminomitosene, a Monofunctional Mitomycin-C Derivative, Alkylates DNA in the Major Groove - Structure and Base-Sequence Specificity of the DNA Adduct and Mechanism of the Alkylation
Kumar GS, Musser SM, Cummings J, Tomasz M
Journal of the American Chemical Society, 118(39), 9209, 1996 |
| 6 |
Alkylation and Cross-Linking of DNA by the Unnatural Enantiomer of Mitomycin-C - Mechanism of the DNA-Sequence Specificity of Mitomycins
Gargiulo D, Musser SS, Yang LH, Fukuyama T, Tomasz M
Journal of the American Chemical Society, 117(37), 9388, 1995 |
| 7 |
Novel Bioreductive Activation Mechanism of Mitomycin-C Derivatives Bearing a Disulfide Substituent in Their Quinone
He QY, Maruenda H, Tomasz M
Journal of the American Chemical Society, 116(20), 9349, 1994 |
