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Nucleosides and nucleotides .159. Synthesis of thietane nucleosides via the pummerer reaction as a key step
被引:37
作者
:
Nishizono, N
论文数:
0
引用数:
0
h-index:
0
机构:
HOKKAIDO UNIV,FAC PHARMACEUT SCI,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN
Nishizono, N
Koike, N
论文数:
0
引用数:
0
h-index:
0
机构:
HOKKAIDO UNIV,FAC PHARMACEUT SCI,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN
Koike, N
Yamagata, Y
论文数:
0
引用数:
0
h-index:
0
机构:
HOKKAIDO UNIV,FAC PHARMACEUT SCI,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN
Yamagata, Y
Fujii, S
论文数:
0
引用数:
0
h-index:
0
机构:
HOKKAIDO UNIV,FAC PHARMACEUT SCI,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN
Fujii, S
Matsuda, A
论文数:
0
引用数:
0
h-index:
0
机构:
HOKKAIDO UNIV,FAC PHARMACEUT SCI,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN
Matsuda, A
机构
:
[1]
HOKKAIDO UNIV,FAC PHARMACEUT SCI,KITA KU,SAPPORO,HOKKAIDO 060,JAPAN
[2]
OSAKA UNIV,FAC PHARMACEUT SCI,SUITA,OSAKA 565,JAPAN
来源
:
TETRAHEDRON LETTERS
|
1996年
/ 37卷
/ 42期
关键词
:
D O I
:
10.1016/0040-4039(96)01719-4
中图分类号
:
O62 [有机化学];
学科分类号
:
070303 ;
081704 ;
摘要
:
New thymine thietane nucleosides 7 and 20 were synthesized via Pummerer rearrangement or the corresponding sulfoxides 5 and 18 in the presence of thymine, TMSOTf, Et(3)N, and ZnI2 as a key step. Copyright (C) 1996 Elsevier Science Ltd
引用
收藏
页码:7569 / 7572
页数:4
相关论文
共 17 条
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共 17 条
[1]
THE CHEMISTRY OF L-ASCORBIC AND D-ISOASCORBIC ACIDS .1. THE PREPARATION OF CHIRAL BUTANETRIOLS AND BUTANETETROLS
[J].
ABUSHANAB, E
论文数:
0
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UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
ABUSHANAB, E
;
VEMISHETTI, P
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h-index:
0
机构:
UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
VEMISHETTI, P
;
LEIBY, RW
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UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
LEIBY, RW
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SINGH, HK
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UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
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UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
WU, DCJ
;
SAIBABA, R
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0
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0
h-index:
0
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UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
UNIV RHODE ISL,DEPT CHEM,KINGSTON,RI 02881
SAIBABA, R
;
PANZICA, RP
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0
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h-index:
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[J].
BISACCHI, GS
论文数:
0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
BISACCHI, GS
;
BRAITMAN, A
论文数:
0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
BRAITMAN, A
;
CIANCI, CW
论文数:
0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
CIANCI, CW
;
CLARK, JM
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0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
CLARK, JM
;
FIELD, AK
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0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
FIELD, AK
;
HAGEN, ME
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0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
HAGEN, ME
;
HOCKSTEIN, DR
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0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
HOCKSTEIN, DR
;
MALLEY, MF
论文数:
0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
MALLEY, MF
;
MITT, T
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0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
MITT, T
;
SLUSARCHYK, WA
论文数:
0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
SLUSARCHYK, WA
;
SUNDEEN, JE
论文数:
0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
SUNDEEN, JE
;
TERRY, BJ
论文数:
0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
TERRY, BJ
;
TUOMARI, AV
论文数:
0
引用数:
0
h-index:
0
机构:
Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08540
TUOMARI, AV
;
WEAVER, ER
论文数:
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