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Replacement of Canonical DNA Nucleobases by Benzotriazole and 1,2,3‐Triazolo[4,5‐ d ]pyrimidine: Synthesis, Fluorescence, and Ambiguous Base Pairing
Author(s) -
Seela Frank,
Jawalekar Anup M.,
Münster Ingo
Publication year - 2005
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.200590052
Subject(s) - chemistry , benzotriazole , nucleobase , pyrimidine , base pair , pairing , stereochemistry , dna , oligonucleotide , fluorescence , base (topology) , oligonucleotide synthesis , nucleic acid , combinatorial chemistry , organic chemistry , biochemistry , mathematical analysis , physics , superconductivity , mathematics , quantum mechanics
The syntheses and the fluorescence properties of 7 H ‐3,6‐dihydro‐1,2,3‐triazolo[4,5‐ d ]pyrimidin‐7‐one 2′‐deoxy‐ β ‐ D ‐ribonucleosides (=2′‐deoxy‐8‐azainosine) 3 ( N 3 ), 15 ( N 2 ), and 16 ( N 1 ) as well as of 1,2,3‐benzotriazole 2′‐ O ‐methyl‐ β ‐ or ‐ α ‐ D ‐ribofuranosides 6 ( N 1 ) and 24 ( N 1 ) are described. Also the fluorescence properties of 1,2,3‐benzotriazole 2′‐deoxy‐ β ‐ D ‐ribofuranosides 4 ( N 1 ) and 5 ( N 2 ) are evaluated. From the nucleosides 3 – 6 , the phosphoramidites 19, 26a, 26b , and 28 are prepared and employed in solid‐phase oligonucleotide synthesis. In 12‐mer DNA duplexes, compound 3 shows similar ambiguous base‐pairing properties as 2′‐deoxyinosine ( 1 ), while the nucleosides 4 – 6 show strong pairing with each other and discriminate very little the four canonical DNA constituents.

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