Zobrazeno 1 - 10
of 13
pro vyhledávání: '"S I, Antsypovich"'
Publikováno v:
Russian Chemical Bulletin. 54:2671-2681
A new versatile method for the preparation of oligonucleotides containing hydrazide groups in any position of the oligonucleotide chain by standard phosphoramidite automated oligonucleotide synthesis is proposed. The method is based on the use of a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c4f9c23afe9e55aa88d140e8a74a647
https://doi.org/10.1007/s11172-006-0175-5
https://doi.org/10.1007/s11172-006-0175-5
Publikováno v:
Russian Journal of Bioorganic Chemistry. 27:184-190
A method for directional introduction of oleylamine residues to any position of oligodeoxyribonucleotides during their automated synthesis was developed. The presence of oleylamine residues in 3'- or 5'-terminal nucleotides was shown to have no effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d6d79f43492d19ddc00c523678cf730
https://doi.org/10.1023/a:1011333421540
https://doi.org/10.1023/a:1011333421540
Autor:
Volkov Em, Elena A. Romanova, S. I. Antsypovich, Zoe A. Shabarova, Vadim N. Tashlitsky, Eugene M. Zubin, Tatiana S. Oretskaya, Nina G. Dolinnaya
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 17:425-440
The synthesis of modified oligodeoxyribonucleotides# containing 2′-amino-2′-deoxyarabinoadenosine residues (aAn) was carried out by means of the standard phosphoramidite chemistry. A high reactivity of such compounds to electrophilic reagents was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c30be7a346623543aea1a10a7092fec4
https://doi.org/10.1080/07328319808005188
https://doi.org/10.1080/07328319808005188
Autor:
Elena A. Romanova, Volkov Em, Tatiana S. Oretskaya, S. I. Antsypovich, Zoe A. Shabarova, Vadim N. Tashlitsky, Marta Blumenfeld
Publikováno v:
Nucleosides and Nucleotides. 15:923-936
A method has been devised to synthesize a DNA-duplex with covalently connected strands. Primary amino group located on one strand is linked to a carboxyl group of the other strand through the agency of a water soluble carbodiimide condensing agent. C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6312edd6ccd0315f819f8fcb89446066
https://doi.org/10.1080/07328319608002138
https://doi.org/10.1080/07328319608002138
Autor:
S. I. Antsypovich, T. S. Oretskaya
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38886e66e6d535049cc72807f4e99c19
https://doi.org/10.1002/chin.199833325
https://doi.org/10.1002/chin.199833325
Publikováno v:
ChemInform. 37
A new versatile method for the preparation of oligonucleotides containing hydrazide groups in any position of the oligonucleotide chain by standard phosphoramidite automated oligonucleotide synthesis is proposed. The method is based on the use of a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::851419166961b86ae40e6bc6c8842aca
https://doi.org/10.1002/chin.200635225
https://doi.org/10.1002/chin.200635225
Publikováno v:
Nucleosides, nucleotidesnucleic acids. 24(3)
We introduce a novel versatile phosphoramidite building block for the modification of oligonucleotides (ONs) with acyl hydrazides on the 5'- or 3'-terminus, or both. The reaction of these hydrazide functionalized ONs with 4-methoxyphenylaldehyde is d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af156f3b793eb963b31b10b58667ffde
https://pubmed.ncbi.nlm.nih.gov/15892260
https://pubmed.ncbi.nlm.nih.gov/15892260
Autor:
V. Gajdos, Elena A. Romanova, C. Tóth, S. Yu. Andreev, S. I. Antsypovich, Tibor Hianik, Tatiana S. Oretskaya
Publikováno v:
Bioelectrochemistry (Amsterdam, Netherlands). 56(1-2)
An effective method for the introduction of oleylamine-modified cytidine units into predetermined position(s) of the oligodeoxyribonucleotide (ON) chain during automated ON synthesis has been developed. The high yields of the condensation products up
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::949786d0887362d8aee61d04e1b1998d
https://pubmed.ncbi.nlm.nih.gov/12009442
https://pubmed.ncbi.nlm.nih.gov/12009442
Publikováno v:
Bioorganicheskaia khimiia. 27(3)
A method for directional introduction of oleylamine residues to any position of oligodeoxyribonucleotides during their automated synthesis was developed. The presence of oleylamine residues in 3'- or 5'-terminal nucleotides was shown to have no effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc56533aa8388d0be1811808b029e78b
https://pubmed.ncbi.nlm.nih.gov/11443944
https://pubmed.ncbi.nlm.nih.gov/11443944
Autor:
E M, Zubin, S I, Antsypovich, T S, Oretskaya, E A, Romanova, E M, Volkov, V N, Tashlitskiĭ, Z A, Shabarova
Publikováno v:
Bioorganicheskaia khimiia. 23(10)
A method for preparing a modified derivative of 2'-amino-2'-deoxy-arabino-adenosine ready for directed insertion into an oligonucleotide chain during solid-phase synthesis was elaborated. A series of the title oligonucleotides (6-25-mers) containing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a39a6b1cf6fd05905c9c4385445da030
https://pubmed.ncbi.nlm.nih.gov/9490617
https://pubmed.ncbi.nlm.nih.gov/9490617