Stereoisomeric C5-C5 '-linked dihydrothymine dimers produced by radiolyticone-electron reduction of thymine derivatives ill anoxic aqueous solution:Structural characteristics in reference to cyclobutane photodimers
T. Ito et al., Stereoisomeric C5-C5 '-linked dihydrothymine dimers produced by radiolyticone-electron reduction of thymine derivatives ill anoxic aqueous solution:Structural characteristics in reference to cyclobutane photodimers, J ORG CHEM, 64(14), 1999, pp. 5100-5108
Radiolytic one-electron reduction of 1-methylthymine (1a) and 1,3-dimethylt
hymine (1b) in anoxic aqueous solution afforded stereoisomeric C5-C5'-linke
d dihydrothymine dimers, fractionated into the meso forms of(5R,5'S)- and (
S5,5'R)-bi-5,6-dihydrothymine (3a,b[meso]) and a racemic mixture of(5R,5'R)
- and (5S,5'S)-bi-5,6-dihydrothymines (3a,b[rac]), along with 5,6-dihydroth
ymines (2a,b). The meso and racemic dimers were produced in almost equivale
nt yields, possessing structural similarity with cis-syn-cyclobutane pyrimi
dine photodimers that are identified as highly mutagenic and carcinogenic p
hotolesions induced by UV light. Similar radiolytic one-electron reduction
of thymidine (1c) resulted in the pseudo-meso form of(5R,5'S)- and (5S,5'R)
-bi-5,6-dihydrothymidine (3c[RS]) and two diastereormers of (5R,5'R)- and (
5S,5'S)-bi-5,6-dihydrothymidine (3c[RR] and 3c[SS]). X-ray crystal structur
es indicated that two pyrimidine rings of the stereoisomeric dimers except
3a[rac] overlap with each other to a considerable extent, as in the cis-syn
-cyclobutane photodimers, The pyrimidine rings of the dimers were twisted a
round 5-Me-C5-C5'-5'-Me by 51.1(2)degrees for 3a[meso], -85.4(4)degrees for
3a[rac], -65(1)degrees for 3b[meso], 43(2)degrees for 3b[rac], and 64.9(4)
degrees for 3c[RS], respectively. It was predicted that the C5-C5'-linked d
ihydrothymine dimers may cause some distortion within a DNA duplex if they
were incorporated. The pH dependence of the reactivities was in accord with
a mechanism of the C5-C5'-linked dimerization by which electron adducts of
1a-c are irreversibly protonated at C6 and the resulting 5,6-dihydrothymin
-5-yl radicals undergo bimolecular coupling.