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- W2024490083 endingPage "4901" @default.
- W2024490083 startingPage "4874" @default.
- W2024490083 abstract "Transition metal-catalyzed modifications of the activated heterocyclic bases of nucleosides as well as DNA or RNA fragments employing traditional cross-coupling methods have been well-established in nucleic acid chemistry. This review covers advances in the area of cross-coupling reactions in which nucleosides are functionalized via direct activation of the C8-H bond in purine and the C5-H or C6-H bond in uracil bases. The review focuses on Pd/Cu-catalyzed couplings between unactivated nucleoside bases with aryl halides. It also discusses cross-dehydrogenative arylations and alkenylations as well as other reactions used for modification of nucleoside bases that avoid the use of organometallic precursors and involve direct C-H bond activation in at least one substrate. The scope and efficiency of these coupling reactions along with some mechanistic considerations are discussed." @default.
- W2024490083 created "2016-06-24" @default.
- W2024490083 creator A5041101731 @default.
- W2024490083 creator A5091412838 @default.
- W2024490083 date "2015-03-17" @default.
- W2024490083 modified "2023-10-07" @default.
- W2024490083 title "Modification of Purine and Pyrimidine Nucleosides by Direct C-H Bond Activation" @default.
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- W2024490083 doi "https://doi.org/10.3390/molecules20034874" @default.
- W2024490083 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6272170" @default.
- W2024490083 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25789821" @default.
- W2024490083 hasPublicationYear "2015" @default.
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