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The photorearrangements of benzyl phenyl selenide and phenyl ribosyl selenide derivatives afford 2-benzyl phenylselenol and 2-ribosyl phenylselenol, respectively which can be isolated as their methyl derivatives. 相似文献
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Absintholide is a new guaianolide dimer whose structure and stereochemistry has been elucidated on the basis of high resolution n.m.r. 相似文献
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A simplified procedure for the preparation of deoxynucleoside methyl- and arylphosphoramidites is described. Both types of phosphoramidites can be conveniently activated by N-methylaniline trifluoracetate for their use in oligodeoxynucleotide synthesis. 相似文献
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Moriou C Thomas M Adeline MT Martin MT Chiaroni A Pochet S Fourrey JL Favre A Clivio P 《The Journal of organic chemistry》2007,72(1):43-50
The 3'-N-sulfamate analogue of thymidylyl(3'-5')thymidine (TnsoT, 1) exhibits a preference for a C3'-endo conformation in the solution and solid states. Its photochemical behavior in solution is compared to that of its natural counterpart, thymidylyl(3'-5')thymidine (TpT, 2), to get further insight into the significance of the C3'-endo conformation on the photoproduct formation at the single-stranded dinucleotide level. Irradiation at 254 nm of 1 led to the same type of photoproducts as observed with 2. However, 1 was significantly more photoreactive than 2, and accordingly, the initial rate of photoproduct formation was enhanced in accordance with its propensity to base stack compared to 2. The corresponding quantum yields were determined and showed that the enhancement factor (1 compared to 2) is moderate for the cyclobutane pyrimidine dimer (CPD) (1.26) and much higher for the (6-4) photoproduct (1.8). These data strongly suggest that the CPD and (6-4) photoproduct arise from distinct minor stacked conformations. 相似文献
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-nonacylated nucleoside phosphoramidites can be prepared in two steps from 2′-deoxynucleosides. Their use in phosphorylation reactions is exemplified. 相似文献
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Gamma-radiolysis DNA products: synthesis of 6-(alpha-thyminyl)-5,6-dihydro-4-thiothymine derivatives
Ortiz Mayo JU Dupradeau FY Guillaume D Fourrey JL Clivio P 《The Journal of organic chemistry》2004,69(14):4797-4801
Far-UV photolysis of 4-thiothymidylyl(3'-5')thymidine led to the formation of three stable derivatives: one resulting from a combination between a 3'-end methylene radical and a 5'-end C(4) radical [4-(alpha-thyminyl) derivative] and two formed after a combination between a 3'-end methylene radical and a 5'-end C(6) radical [6-(alpha-thyminyl) derivative]. In the latter series, two stereochemical pathways took place during the reaction between the methylene and C(6) radicals. The major pathway occurred when the 5'-base glycosidic bond had an anti conformation leading to an S configuration of the C(6) Tp-end. The minor pathway, which had never been reported before in this series, involved a 5'-base in a syn conformation leading consequently to the R configuration at the C(6) Tp-end. The 5,6-dihydrothymine moiety of these two adducts presented a 5,6-trans diaxial substitution that resulted from the epimerization, at the 5,6-dihydropyrimidine 5-position, of a less stable cis-disubstituted intermediate. 相似文献
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Absinthin, a constituent of . , has been given structure . 相似文献