Олигорибонуклеотиды, содержащие перфторарилазидную группу в гетероциклическом основании — новые фотоаффинные реагенты для модификации биополимеров
Далее необходимо было выяснить стабильность бромсодержащих нуклеозидов в процессе олигонуклеотидного синтеза. Судя по литературным данным, атом брома в гетероциклическом основании остается инертным ко всем реагентам, используемым в ходе твердофазного синтеза, однако последующее деблокирование экзоциклических аминогрупп и удаления олигонуклеотида с полимера с помощью конц. NHjOH в жестких условиях… Читать ещё >
Содержание
- Список принятых сокращений и обозначений
1. Функционализация гетероциклических оснований олигонуклеотидов с 9 целью создания реагентов для селективного воздействия на биополимеры (обзор литературы)
1.1. Функционализация гетероциклических оснований олигонуклеотидов
1.1.1. Экзоциклические аминогруппы гетероциклических оснований
1.1.1.1. Ж-Положение цитозина
1.1.1.2. Н2-Положение гуанина и Кб-положение аденина
1.1.2. С5-Положение пиримидинов
1.1.3. С8-Положение пуринов '
1.2. Производные олигонуклеотидов с реакционноспособными группами 37 в гетероцикле как инструменты селективного воздействия на биополимеры
1.2.1. Алкилирутощие производные олигонуклеотидов
1.2.2. Фотоактивируемые производные олигонуклеотидов
1.2.3. Реагенты для расщепления НК
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