GENERAL-METHOD FOR THE PREPARATION OF N-3-SUBSTITUTED AND O-4-SUBSTITUTED URIDINE DERIVATIVES BY PHASE-TRANSFER REACTIONS

被引：61

作者：

SEKINE, M

机构：

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1989年 / 54卷 / 10期

关键词：

D O I：

10.1021/jo00271a015

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

收藏

页码：2321 / 2326

页数：6

相关论文

共 57 条

[1] BAERWOLFF D, 1980, Patent No. 140254
[2] ONE-STEP PROTECTION OF THE NUCLEOSIDE BASE IN THYMIDINE AND URIDINE
CLAESEN, CAA
PISTORIUS, AMA
TESSER, GI
[J]. TETRAHEDRON LETTERS, 1985, 26 (32) : 3859 - 3862
[3] 4-(1,2,4-TRIAZOL-1-YL) AND 4-(3-NITRO-1,2,4-TRIAZOL-1-YL)-1-(BETA-D-2,3,5-TRI-O-ACETYLARABINOFURANOSYL)PYRIMIDIN-2(1H)-ONES - VALUABLE INTERMEDIATES IN THE SYNTHESIS OF DERIVATIVES OF "1-(BETA-D-ARABINOFURANOSYL)CYTOSINE (ARA-C)
DIVAKAR, KJ
REESE, CB
[J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1982, (05): : 1171 - 1176
[4] HARTOG JAJ, 1982, BIOCHEMISTRY-US, V21, P1009
[5] A NEW METHOD FOR THE SYNTHESIS OF OLIGODEOXYRIBONUCLEOTIDES BEARING A 5'-TERMINAL PHOSPHATE GROUP
HATA, T
KAMIMURA, T
URAKAMI, K
KOHNO, K
SEKINE, M
KUMAGAI, I
SHINOZAKI, K
MIURA, K
[J]. CHEMISTRY LETTERS, 1987, (01) : 117 - 120
[6] ALLYLOXYCARBONYL GROUP - A VERSATILE BLOCKING GROUP FOR NUCLEOTIDE SYNTHESIS
HAYAKAWA, Y
KATO, H
UCHIYAMA, M
KAJINO, H
NOYORI, R
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1986, 51 (12) : 2400 - 2402
[7] SYNTHESIS AND HYBRIDIZATION STUDIES ON 2 COMPLEMENTARY NONA(2'-O-METHYL)RIBONUCLEOTIDES
INOUE, H
HAYASE, Y
IMURA, A
IWAI, S
MIURA, K
OHTSUKA, E
[J]. NUCLEIC ACIDS RESEARCH, 1987, 15 (15) : 6131 - 6148
[8] INOUE H, 1985, NUCLEIC ACIDS S SER, V16, P1650
[9] STRUCTURAL ASSIGNMENT OF N-3-ACYLATED URIDINE DERIVATIVES BY MEANS OF C-13 NMR-SPECTROSCOPY
KAMIMURA, T
MASEGI, T
SEKINE, M
HATA, T
[J]. TETRAHEDRON LETTERS, 1984, 25 (38) : 4241 - 4244
[10] A NEW PROTECTING TACTICS FOR THE URACIL RESIDUE IN OLIGORIBONUCLEOTIDE SYNTHESIS
KAMIMURA, T
MASEGI, T
URAKAMI, K
HONDA, S
SEKINE, M
HATA, T
[J]. CHEMISTRY LETTERS, 1983, (07) : 1051 - 1054

← 1 2 3 4 5 6 →