发明名称 |
INTERMEDIATES FOR OLIGONUCLEOTIDE SYNTHESIS |
摘要 |
A compound of formula (I) where B<1> is a radical of a nucleoside base, R<1> is hydrogen or a hydroxy-protecting group, R<2> is hydrogen, hydroxy or a 2' nucleoside-modifying atom or group, R<3> is an unsubstituted or substituted C1 to C10 alkyl, C2 to C10 alkenyl, C4 to C10 cycloalkylalkyl, C6 to C10 aryl or C7 to C13 aralkyl group, and Z is halogen or a group of formula (II) where R<4> and R<5> are each independently an unsubstituted or substituted C1 to C10 alkyl, C2 to C10 alkenyl, C4 to C10 cycloalkylalkyl, C6 to C10 aryl or C7 to C13 aralkyl group, or R<4> is said group and R<5> is hydrogen, or R<4> and R<5> together with the nitrogen atom to which they are attached denote a five- to thirteen-membered heterocyclic ring, or Z is a group of formula (III): Nuc-O-, where Nuc is the residue of a natural or synthetic nucleoside or oligonucleotide after removal of a 5'-hydroxyl group therefrom attached through a 5' methylene thereof to the indicated oxygen atom. 00000 |
申请公布号 |
WO9747636(A3) |
申请公布日期 |
1998.02.12 |
申请号 |
WO1997GB01490 |
申请日期 |
1997.06.03 |
申请人 |
NOVARTIS AG;COLLINGWOOD, STEPHEN, PAUL;MOSER, HEINZ, ERNST;ALTMANN, KARL-HEINZ;DOUGLAS, MARK, EDWARD |
发明人 |
COLLINGWOOD, STEPHEN, PAUL;MOSER, HEINZ, ERNST;ALTMANN, KARL-HEINZ;DOUGLAS, MARK, EDWARD |
分类号 |
C07H19/06;C07H19/04;C07H19/16;C07H21/00 |
主分类号 |
C07H19/06 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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