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Sulfonium derivatives of thioxanthenone, a new class of photodetritylating agents for microarray oligonucleotide synthesis Full article

Journal Russian Journal of Bioorganic Chemistry
ISSN: 1068-1620
Output data Year: 2010, Volume: 36, Number: 1, Pages: 130-132 Pages count : DOI: 10.1134/S1068162010010152
Tags photogenerators of acids; oligodeoxyribonucleotides; thioxanthenone; trityl cation
Authors Sinyakov A. N. 1 , Ryabinin A. A. 1 , Maksakova G. A. 1 , Shelkovnikov V. V. 2 , Loskutov V. A. 2 , Vasil'ev E. V. 2 , Shekleina N. V. 2
Affiliations
1 (Данные Web of science) Russian Acad Sci, Inst Chem Biol & Fundamental Med, Siberian Branch, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, Siberian Branch, Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: The usability of a new class of photo acids, namely, sulfonium hexaphosphates based on thioxanthenone, for the removal of the dimethoxytrityl protective group in the process of oligonucleotide synthesis has been studied in order to search for new detritylating agents for microarray oligodeoxyribonucleotide synthesis. 2,4-Diethyl-9-oxo-10-(4-heptyloxyphenyl)-9H-thioxanthenium hexafluorophosphate has been successfully used for the solid-phase synthesis of (dT)(10).
Cite: Sinyakov A.N. , Ryabinin A.A. , Maksakova G.A. , Shelkovnikov V.V. , Loskutov V.A. , Vasil'ev E.V. , Shekleina N.V.
Sulfonium derivatives of thioxanthenone, a new class of photodetritylating agents for microarray oligonucleotide synthesis
Russian Journal of Bioorganic Chemistry. 2010. V.36. N1. P.130-132. DOI: 10.1134/S1068162010010152 WOS Scopus РИНЦ OpenAlex
Original: Синяков А.Н. , Рябинин А.А. , Максакова Г.А. , Шелковников В.В. , Лоскутов В.А. , Васильев Е.В. , Васильева Н.В.
Сульфониевые производные тиоксантенона – новый класс соединений для фотодетритилирования в микрочиповом олигонуклеотидном синтезе
Биоорганическая химия (RUSS J BIOORG CHEM+). 2010. Т.31. №1. С.139-141. РИНЦ
Dates:
Published print: Jan 1, 2010
Published online: Feb 2, 2010
Identifiers:
Web of science: WOS:000274211500015
Scopus: 2-s2.0-77649092151
Elibrary: 15313256
OpenAlex: W2141938212
Citing:
DB Citing
Web of science 6
Scopus 5
Elibrary 7
OpenAlex 5
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