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A new route to spirooxindoles
被引:203
作者
:
Hilton, ST
论文数:
0
引用数:
0
h-index:
0
机构:
Kingston Univ, Sch Chem & Pharmaceut Sci, Kingston upon Thames KT1 2EE, Surrey, England
Kingston Univ, Sch Chem & Pharmaceut Sci, Kingston upon Thames KT1 2EE, Surrey, England
Hilton, ST
[
1
]
Ho, TCT
论文数:
0
引用数:
0
h-index:
0
机构:
Kingston Univ, Sch Chem & Pharmaceut Sci, Kingston upon Thames KT1 2EE, Surrey, England
Kingston Univ, Sch Chem & Pharmaceut Sci, Kingston upon Thames KT1 2EE, Surrey, England
Ho, TCT
[
1
]
Pljevaljcic, G
论文数:
0
引用数:
0
h-index:
0
机构:
Kingston Univ, Sch Chem & Pharmaceut Sci, Kingston upon Thames KT1 2EE, Surrey, England
Kingston Univ, Sch Chem & Pharmaceut Sci, Kingston upon Thames KT1 2EE, Surrey, England
Pljevaljcic, G
[
1
]
论文数:
引用数:
h-index:
机构:
Jones, K
[
1
]
机构
:
[1]
Kingston Univ, Sch Chem & Pharmaceut Sci, Kingston upon Thames KT1 2EE, Surrey, England
来源
:
ORGANIC LETTERS
|
2000年
/ 2卷
/ 17期
关键词
:
D O I
:
10.1021/ol0061642
中图分类号
:
O62 [有机化学];
学科分类号
:
070303 ;
081704 ;
摘要
:
[GRAPHICS] Reaction of indole amides 5 with tributylstannane gave spiroindolenines 9 which are readily converted into spiropyrrolidinyloxindoles. This tricyclic system is found In a number of interesting natural products.
引用
收藏
页码:2639 / 2641
页数:3
相关论文
共 25 条
[21]
Total synthesis of (+)-elacomine and (-)-isoelacomine, two hitherto unnamed oxindole alkaloids from Elaeagnus commutata
Pellegrini, C
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0
引用数:
0
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0
机构:
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
Pellegrini, C
Weber, M
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ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
Weber, M
Borschberg, HJ
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0
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ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
Borschberg, HJ
[J].
HELVETICA CHIMICA ACTA,
1996,
79
(01)
: 151
-
168
[22]
SYNTHESIS OF THE OXINDOLE ALKALOID (-)-HORSFILINE
PELLEGRINI, C
论文数:
0
引用数:
0
h-index:
0
机构:
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
PELLEGRINI, C
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0
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0
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ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
STRASSLER, C
WEBER, M
论文数:
0
引用数:
0
h-index:
0
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ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
WEBER, M
BORSCHBERG, HJ
论文数:
0
引用数:
0
h-index:
0
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ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
BORSCHBERG, HJ
[J].
TETRAHEDRON-ASYMMETRY,
1994,
5
(10)
: 1979
-
1992
[23]
STUDIES DIRECTED TOWARD THE ENANTIOSPECIFIC SYNTHESIS OF GARDNERIA, VOACANGA, AND ALSTONIA OXINDOLE ALKALOIDS
PETERSON, AC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
PETERSON, AC
COOK, JM
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0
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0
h-index:
0
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UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
COOK, JM
[J].
JOURNAL OF ORGANIC CHEMISTRY,
1995,
60
(01)
: 120
-
129
[24]
NUCLEOPHILIC-TYPE RADICAL CYCLIZATIONS OF INDOLES - CONVERSION OF 2-CYANO 3-SUBSTITUTED INDOLES TO SPIRO-ANNELATED INDOLINES AND TETRAHYDROCARBAZOLONES
YANG, CC
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NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
YANG, CC
CHANG, HT
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NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
CHANG, HT
FANG, JM
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NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
FANG, JM
[J].
JOURNAL OF ORGANIC CHEMISTRY,
1993,
58
(11)
: 3100
-
3105
[25]
Diastereospecific synthesis of ketooxindoles. Potential intermediates for the synthesis of alstonisine as well as for Voachalotine related oxindole alkaloids
Yu, P
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
Yu, P
Cook, JM
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0
引用数:
0
h-index:
0
机构:
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
Cook, JM
[J].
TETRAHEDRON LETTERS,
1997,
38
(51)
: 8799
-
8802
←
1
2
3
→
共 25 条
[21]
Total synthesis of (+)-elacomine and (-)-isoelacomine, two hitherto unnamed oxindole alkaloids from Elaeagnus commutata
Pellegrini, C
论文数:
0
引用数:
0
h-index:
0
机构:
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
Pellegrini, C
Weber, M
论文数:
0
引用数:
0
h-index:
0
机构:
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
Weber, M
Borschberg, HJ
论文数:
0
引用数:
0
h-index:
0
机构:
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
Borschberg, HJ
[J].
HELVETICA CHIMICA ACTA,
1996,
79
(01)
: 151
-
168
[22]
SYNTHESIS OF THE OXINDOLE ALKALOID (-)-HORSFILINE
PELLEGRINI, C
论文数:
0
引用数:
0
h-index:
0
机构:
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
PELLEGRINI, C
STRASSLER, C
论文数:
0
引用数:
0
h-index:
0
机构:
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
STRASSLER, C
WEBER, M
论文数:
0
引用数:
0
h-index:
0
机构:
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
WEBER, M
BORSCHBERG, HJ
论文数:
0
引用数:
0
h-index:
0
机构:
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
ETH ZENTRUM,ORGAN CHEM LAB,CH-8092 ZURICH,SWITZERLAND
BORSCHBERG, HJ
[J].
TETRAHEDRON-ASYMMETRY,
1994,
5
(10)
: 1979
-
1992
[23]
STUDIES DIRECTED TOWARD THE ENANTIOSPECIFIC SYNTHESIS OF GARDNERIA, VOACANGA, AND ALSTONIA OXINDOLE ALKALOIDS
PETERSON, AC
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
PETERSON, AC
COOK, JM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
COOK, JM
[J].
JOURNAL OF ORGANIC CHEMISTRY,
1995,
60
(01)
: 120
-
129
[24]
NUCLEOPHILIC-TYPE RADICAL CYCLIZATIONS OF INDOLES - CONVERSION OF 2-CYANO 3-SUBSTITUTED INDOLES TO SPIRO-ANNELATED INDOLINES AND TETRAHYDROCARBAZOLONES
YANG, CC
论文数:
0
引用数:
0
h-index:
0
机构:
NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
YANG, CC
CHANG, HT
论文数:
0
引用数:
0
h-index:
0
机构:
NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
CHANG, HT
FANG, JM
论文数:
0
引用数:
0
h-index:
0
机构:
NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
NATL TAIWAN UNIV,DEPT CHEM,TAIPEI 10617,TAIWAN
FANG, JM
[J].
JOURNAL OF ORGANIC CHEMISTRY,
1993,
58
(11)
: 3100
-
3105
[25]
Diastereospecific synthesis of ketooxindoles. Potential intermediates for the synthesis of alstonisine as well as for Voachalotine related oxindole alkaloids
Yu, P
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
Yu, P
Cook, JM
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
UNIV WISCONSIN,DEPT CHEM,MILWAUKEE,WI 53201
Cook, JM
[J].
TETRAHEDRON LETTERS,
1997,
38
(51)
: 8799
-
8802
←
1
2
3
→