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New acid photogenerators based on thioxanthen-9-one sulfonium derivatives for detritylation in the oligonucleotide synthesis Научная публикация

Журнал Russian Chemical Bulletin
ISSN: 1066-5285 , E-ISSN: 1573-9171
Вых. Данные Год: 2011, Том: 60, Номер: 3, Страницы: 561-569 Страниц : DOI: 10.1007/s11172-011-0087-x
Ключевые слова photoactivators of detritylation; acid photogenerators; trityl cation; thioxan-thenone derivatives
Авторы Shelkovnikov V. V. 1 , Loskutov V. A. 1 , Vasil'ev E. V. 1,2 , Shekleina N. V. 1 , Ryabinin V. A. 3 , Sinyakov A. N. 3
Организации
1 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Novosibirsk State Univ, Res Educ Ctr Mol Design & Environm Safe Technol, Novosibirsk 630090, Russia
3 (Данные Web of science) Russian Acad Sci, Siberian Branch, Inst Chem Biol & Fundamental Med, Novosibirsk 630090, Russia

Реферат: Photochemical activity of a number of cationic thioxanthen-9-one derivatives for the formation of the trityl cation was studied, which resulted in the selection of compounds suitable for photodetritylation. 10-(4-Heptyloxyphenyl)-9-oxo-2-(N,N,N-triethylammonio)methyl-9H-thioxanthenium bis(hexafluorophosphate) and 2-methyl-, 2-(2-methyl-1-propanoyl-2-tosyl)-, 1-chloro-4-propoxy-, and 2,4-diethyl-10-(4-heptyloxyphenyl)-9-oxo-9H-thioxanthenium hexafluorophosphates were found to be photoactivators of detritylation of 5'-O-(4,4'-dimethoxytrityl)thymidine. The detritylation reaction is the most efficient in dichloromethane. 2,4-Diethyl-10-(4-heptyloxyphenyl)-9-oxo-9H-thioxanthenium hexafluorophosphate was used as a detritylation photoactivator in the oligonucleotide synthesis using an automated DNA synthesizer. The yield in the elongation step of the oligonucleotide chain was 98%.
Библиографическая ссылка: Shelkovnikov V.V. , Loskutov V.A. , Vasil'ev E.V. , Shekleina N.V. , Ryabinin V.A. , Sinyakov A.N.
New acid photogenerators based on thioxanthen-9-one sulfonium derivatives for detritylation in the oligonucleotide synthesis
Russian Chemical Bulletin. 2011. V.60. N3. P.561-569. DOI: 10.1007/s11172-011-0087-x WOS Scopus РИНЦ OpenAlex
Даты:
Опубликована в печати: 1 мар. 2011 г.
Опубликована online: 6 сент. 2011 г.
Идентификаторы БД:
Web of science: WOS:000294715900026
Scopus: 2-s2.0-80052703506
РИНЦ: 18005086
OpenAlex: W2011518617
Цитирование в БД:
БД Цитирований
Web of science 8
Scopus 9
РИНЦ 10
OpenAlex 11
Альметрики: