Zobrazeno 1 - 10
of 37
pro vyhledávání: '"John Pataki"'
Publikováno v:
The Journal of Organic Chemistry. 63:6405-6408
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0d895069d51c5c83717203c492568b
https://doi.org/10.1021/jo9806613
https://doi.org/10.1021/jo9806613
Publikováno v:
Tetrahedron. 53:15947-15956
Efficient syntheses of the 3-, 9-, 10-, and 11-phenol isomers of dibenz[a,c]anthracene (DBa,cA) and 2,3-dihydroxy-DBa,cA are described. Bromination of DBa,cA with bromine in CH2Cl2 gave 10-bromo-DBa,cA and not 9-bromo-DBa,cA predicted theoretically.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0015315408b4a0d0de2885178dde4c1
https://doi.org/10.1016/s0040-4020(97)10065-5
https://doi.org/10.1016/s0040-4020(97)10065-5
Publikováno v:
Cancer Letters. 110:249-252
The mutational specificity of the syn dihydrodiol epoxide of 5-methylchrysene in the supF gene of the pSP189 vector was examined. Transversion mutations at GC pairs predominated with G --> T and G --> C changes accounting for 42 and 21% of total base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a2b73b27de5122048015e2f101c930f
https://doi.org/10.1016/s0304-3835(96)04506-5
https://doi.org/10.1016/s0304-3835(96)04506-5
Publikováno v:
Polycyclic Aromatic Compounds. 5:43-50
The active metabolites of alternant carcinogenic polycyclic aromatic hydrocarbons (PAH) with 4-5 fused rings are now readily available through synthesis. Development of new synthetic methodologies that are more efficient and are also applicable to la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97dc5679f2e444d0b31f39712a04c37d
https://doi.org/10.1080/10406639408015154
https://doi.org/10.1080/10406639408015154
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21cc8f78fe3eaee46857eb2fabfdcf3c
https://doi.org/10.1002/chin.199125146
https://doi.org/10.1002/chin.199125146
Publikováno v:
ChemInform. 29
Efficient syntheses of the 3-, 9-, 10-, and 11-phenol isomers of dibenz[a,c]anthracene (DBa,cA) and 2,3-dihydroxy-DBa,cA are described. Bromination of DBa,cA with bromine in CH2Cl2 gave 10-bromo-DBa,cA and not 9-bromo-DBa,cA predicted theoretically.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69e2708ddcacfdb956b4a12942212768
https://doi.org/10.1002/chin.199809103
https://doi.org/10.1002/chin.199809103
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b5fe6bfde36260a6ac776d7899a9723
https://doi.org/10.1002/chin.199908109
https://doi.org/10.1002/chin.199908109
Publikováno v:
Chemical Research in Toxicology. 4:305-310
Eight deoxyribonucleoside adducts formed from reactions of syn-5-methylchrysene 1,2-dihydrodiol 3,4-epoxide with DNA or with nucleotides were characterized spectroscopically. The adducts arose from both cis and trans opening of the epoxide ring at C4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6778d46d963d39e76c33a0d65c9676d4
https://doi.org/10.1021/tx00021a008
https://doi.org/10.1021/tx00021a008
Publikováno v:
The Journal of Organic Chemistry. 56:1210-1217
Alkylation of enamines and enamine salts followed by a cyclodehydration and dehydrogenation provides an efficient synthetic approach to a wide range of polycyclic aromatic compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::570c0303ccc54a6a367e6fe04787d0cf
https://doi.org/10.1021/jo00003a050
https://doi.org/10.1021/jo00003a050
Autor:
C. A. H. Bigger, D.J. Flickinger, Ronald G. Harvey, Anthony Dipple, John Pataki, J. Strandberg
Publikováno v:
Carcinogenesis. 11(12)
An SV40-based pS189 shuttle vector, which contained a supF target gene and was replicated in human cells (Ad293), was used to determine the mutational specificity of anti 5-methylchrysene 1,2-dihydrodiol 3,4-epoxide, the active metabolite of the envi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bbc02cb0b7f78f21ed522317dfa550f
https://pubmed.ncbi.nlm.nih.gov/2176139
https://pubmed.ncbi.nlm.nih.gov/2176139