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ALK-1-YNYLLEAD TRIACETATES AS ALK-1-YNYL CARBOCATION EQUIVALENTS - THE ALPHA-ALK-1-YNYLATION OF BETA-DICARBONYL COMPOUNDS AND NITRONATE SALTS
被引:17
作者
:
MOLONEY, MG
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
MOLONEY, MG
[
1
]
PINHEY, JT
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
PINHEY, JT
[
1
]
ROCHE, EG
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
ROCHE, EG
[
1
]
机构
:
[1]
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
来源
:
TETRAHEDRON LETTERS
|
1986年
/ 27卷
/ 41期
关键词
:
D O I
:
10.1016/S0040-4039(00)85124-2
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:5025 / 5028
页数:4
相关论文
共 7 条
[1]
NUCLEOPHILIC ETHYNYL GROUP EQUIVALENT AND ITS USE IN CONJUGATE ADDITION TO ALPHA,BETA-ENONES
COREY, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA
HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA
COREY, EJ
WOLLENBERG, RH
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA
HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA
WOLLENBERG, RH
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1974,
96
(17)
: 5581
-
5583
[2]
DICKSTEIN JI, 1978, CHEM CARBON CARBON 2, P911
[3]
CHLOROACETYLENES AS MICHAEL ACCEPTORS .2. DIRECT ETHYNYLATION AND VINYLATION OF TERTIARY ENOLATES
KENDE, AS
论文数:
0
引用数:
0
h-index:
0
KENDE, AS
FLUDZINSKI, P
论文数:
0
引用数:
0
h-index:
0
FLUDZINSKI, P
[J].
TETRAHEDRON LETTERS,
1982,
23
(23)
: 2373
-
2376
[4]
REACTION OF ARYLTRIALKYLSTANNANES WITH LEAD-TETRAACETATE - A CONVENIENT ROUTE TO ARYLLEAD TRIACETATES
KOZYROD, RP
论文数:
0
引用数:
0
h-index:
0
KOZYROD, RP
MORGAN, J
论文数:
0
引用数:
0
h-index:
0
MORGAN, J
PINHEY, JT
论文数:
0
引用数:
0
h-index:
0
PINHEY, JT
[J].
AUSTRALIAN JOURNAL OF CHEMISTRY,
1985,
38
(08)
: 1147
-
1153
[5]
ARYLATION WITH ARYLLEAD TRIACETATES PRODUCED INSITU BY MERCURY LEAD EXCHANGE
KOZYROD, RP
论文数:
0
引用数:
0
h-index:
0
KOZYROD, RP
PINHEY, JT
论文数:
0
引用数:
0
h-index:
0
PINHEY, JT
[J].
AUSTRALIAN JOURNAL OF CHEMISTRY,
1985,
38
(08)
: 1155
-
1161
[6]
NUCLEOPHILIC-SUBSTITUTION AT ACETYLENIC CARBON - LAST HOLDOUT
MILLER, SI
论文数:
0
引用数:
0
h-index:
0
机构:
IIT,DEPT CHEM,CHICAGO,IL 60616
IIT,DEPT CHEM,CHICAGO,IL 60616
MILLER, SI
DICKSTEIN, JI
论文数:
0
引用数:
0
h-index:
0
机构:
IIT,DEPT CHEM,CHICAGO,IL 60616
IIT,DEPT CHEM,CHICAGO,IL 60616
DICKSTEIN, JI
[J].
ACCOUNTS OF CHEMICAL RESEARCH,
1976,
9
(10)
: 358
-
363
[7]
ALPHA-ALKENYLATION OF BETA-DICARBONYL COMPOUNDS WITH ALK-1-ENYL-LEAD TRIACETATES
MOLONEY, MG
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
MOLONEY, MG
PINHEY, JT
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
PINHEY, JT
[J].
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS,
1984,
(15)
: 965
-
966
←
1
→
共 7 条
[1]
NUCLEOPHILIC ETHYNYL GROUP EQUIVALENT AND ITS USE IN CONJUGATE ADDITION TO ALPHA,BETA-ENONES
COREY, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA
HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA
COREY, EJ
WOLLENBERG, RH
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA
HARVARD UNIV, DEPT CHEM, CAMBRIDGE, MA 02138 USA
WOLLENBERG, RH
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1974,
96
(17)
: 5581
-
5583
[2]
DICKSTEIN JI, 1978, CHEM CARBON CARBON 2, P911
[3]
CHLOROACETYLENES AS MICHAEL ACCEPTORS .2. DIRECT ETHYNYLATION AND VINYLATION OF TERTIARY ENOLATES
KENDE, AS
论文数:
0
引用数:
0
h-index:
0
KENDE, AS
FLUDZINSKI, P
论文数:
0
引用数:
0
h-index:
0
FLUDZINSKI, P
[J].
TETRAHEDRON LETTERS,
1982,
23
(23)
: 2373
-
2376
[4]
REACTION OF ARYLTRIALKYLSTANNANES WITH LEAD-TETRAACETATE - A CONVENIENT ROUTE TO ARYLLEAD TRIACETATES
KOZYROD, RP
论文数:
0
引用数:
0
h-index:
0
KOZYROD, RP
MORGAN, J
论文数:
0
引用数:
0
h-index:
0
MORGAN, J
PINHEY, JT
论文数:
0
引用数:
0
h-index:
0
PINHEY, JT
[J].
AUSTRALIAN JOURNAL OF CHEMISTRY,
1985,
38
(08)
: 1147
-
1153
[5]
ARYLATION WITH ARYLLEAD TRIACETATES PRODUCED INSITU BY MERCURY LEAD EXCHANGE
KOZYROD, RP
论文数:
0
引用数:
0
h-index:
0
KOZYROD, RP
PINHEY, JT
论文数:
0
引用数:
0
h-index:
0
PINHEY, JT
[J].
AUSTRALIAN JOURNAL OF CHEMISTRY,
1985,
38
(08)
: 1155
-
1161
[6]
NUCLEOPHILIC-SUBSTITUTION AT ACETYLENIC CARBON - LAST HOLDOUT
MILLER, SI
论文数:
0
引用数:
0
h-index:
0
机构:
IIT,DEPT CHEM,CHICAGO,IL 60616
IIT,DEPT CHEM,CHICAGO,IL 60616
MILLER, SI
DICKSTEIN, JI
论文数:
0
引用数:
0
h-index:
0
机构:
IIT,DEPT CHEM,CHICAGO,IL 60616
IIT,DEPT CHEM,CHICAGO,IL 60616
DICKSTEIN, JI
[J].
ACCOUNTS OF CHEMICAL RESEARCH,
1976,
9
(10)
: 358
-
363
[7]
ALPHA-ALKENYLATION OF BETA-DICARBONYL COMPOUNDS WITH ALK-1-ENYL-LEAD TRIACETATES
MOLONEY, MG
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
MOLONEY, MG
PINHEY, JT
论文数:
0
引用数:
0
h-index:
0
机构:
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
UNIV SYDNEY,DEPT ORGAN CHEM,SYDNEY,NSW 2006,AUSTRALIA
PINHEY, JT
[J].
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS,
1984,
(15)
: 965
-
966
←
1
→