(METHOXYETHOXY)METHYL GROUP - NEW AMIDE AND HYDROXYL PROTECTING GROUPS OF URIDINE IN OLIGONUCLEOTIDE SYNTHESIS

被引：13

作者：

ITO, T ^{[1
]}

UEDA, S ^{[1
]}

TAKAKU, H ^{[1
]}

机构：

[1] CHIBA INST TECHNOL,BIOORGAN CHEM LAB,NARASHINO,CHIBA 275,JAPAN

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1986年 / 51卷 / 06期

关键词：

D O I：

10.1021/jo00356a033

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：931 / 933

页数：3

共 20 条

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[6]

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[7] STRUCTURAL ASSIGNMENT OF N-3-ACYLATED URIDINE DERIVATIVES BY MEANS OF C-13 NMR-SPECTROSCOPY [J].

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[8] A NEW PROTECTING TACTICS FOR THE URACIL RESIDUE IN OLIGORIBONUCLEOTIDE SYNTHESIS [J].

KAMIMURA, T ;

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HONDA, S ;

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CHEMISTRY LETTERS, 1983, (07) :1051-1054

[9] PROTECTION OF IMIDE GROUP OF URACIL MOIETY BY MEANS OF 2,2,2-TRICHLORO-TERT-BUTYLOXYCARBONYL CHLORIDE - A SELECTIVE SYNTHESIS OF 2'-O-METHYLURIDINE [J].

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[10]

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