发明名称 Protecting group for synthesizing oligonucleotide analogs
摘要 A 2-N-amidoethyl protected nucleoside analog phosphoramidite of formula (1): is useful in the synthesis of a wide variety of oligonucleotide analogs. Coupling yields with phosphoramidite (1) in solution or solid phase oligonucleotide analog synthesis are high and the 2-N-amidoethyl protecting group can be removed easily under standard conditions.
申请公布号 US5959099(A) 申请公布日期 1999.09.28
申请号 US19980103399 申请日期 1998.06.24
申请人 ISIS PHARMACEUTICALS, INC. 发明人 CHERUVALLATH, ZACHARIA S.;CAPALDI, DANIEL C.;RAVIKUMAR, VASULINGA T.;COLE, DOUGLAS L.
分类号 C07C253/00;C07C255/50;C07H19/10;C07H19/20;C07H21/00;(IPC1-7):C07H19/04 主分类号 C07C253/00
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