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Enantioselective Diels-Alder reactions between cyclopentadiene and alpha,beta-acetylenic aldehydes catalyzed by a chiral super Lewis acid
被引:44
作者
:
Corey, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
Dept. of Chem. and Chemical Biology, Harvard University, Cambridge
Corey, EJ
Lee, TW
论文数:
0
引用数:
0
h-index:
0
机构:
Dept. of Chem. and Chemical Biology, Harvard University, Cambridge
Lee, TW
机构
:
[1]
Dept. of Chem. and Chemical Biology, Harvard University, Cambridge
来源
:
TETRAHEDRON LETTERS
|
1997年
/ 38卷
/ 33期
关键词
:
D O I
:
10.1016/S0040-4039(97)01287-2
中图分类号
:
O62 [有机化学];
学科分类号
:
070303 ;
081704 ;
摘要
:
The first examples of catalytic enantioselective Diels-Alder reactions of cyclopentadiene and alpha,beta-acetyleptic aldehydes such as Bu3SnC=CCHO are described. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:5755 / 5758
页数:4
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EMORY UNIV,SANFORD S ATWOOD CHEM CTR,ATLANTA,GA 30322
EMORY UNIV,SANFORD S ATWOOD CHEM CTR,ATLANTA,GA 30322
Liebeskind, LS
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
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DEMONSTRATION OF THE SYNTHETIC POWER OF OXAZABOROLIDINE-CATALYZED ENANTIOSELECTIVE DIELS-ALDER REACTIONS BY VERY EFFICIENT ROUTES TO CASSIOL AND GIBBERELLIC-ACID
COREY, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University Cambridge, Massachusetts
COREY, EJ
GUZMANPEREZ, A
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University Cambridge, Massachusetts
GUZMANPEREZ, A
LOH, TP
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0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University Cambridge, Massachusetts
LOH, TP
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
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: 3611
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3612
[3]
ENANTIOSELECTIVE TOTAL SYNTHESIS OF GRACILIN-B AND GRACILIN-C USING CATALYTIC ASYMMETRIC DIELS-ALDER METHODOLOGY
COREY, EJ
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Department of Chemistry, Harvard University, Cambridge
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LETAVIC, MA
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0
引用数:
0
h-index:
0
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Department of Chemistry, Harvard University, Cambridge
LETAVIC, MA
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
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9617
[4]
THE ORIGIN OF GREATER THAN 200/1 ENANTIOSELECTIVITY IN A CATALYTIC DIELS-ALDER REACTION AS REVEALED BY PHYSICAL AND CHEMICAL STUDIES
COREY, EJ
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引用数:
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0
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Department of Chemistry, Harvard University, Cambridge
COREY, EJ
LOH, TP
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0
引用数:
0
h-index:
0
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Department of Chemistry, Harvard University, Cambridge
LOH, TP
ROPER, TD
论文数:
0
引用数:
0
h-index:
0
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Department of Chemistry, Harvard University, Cambridge
ROPER, TD
AZIMIOARA, MD
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0
引用数:
0
h-index:
0
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Department of Chemistry, Harvard University, Cambridge
AZIMIOARA, MD
NOE, MC
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0
引用数:
0
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0
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Department of Chemistry, Harvard University, Cambridge
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[J].
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The formyl C-H--O hydrogen bond as a key to transition-state organization in enantioselective allylation, aldol and Diels-Alder reactions catalyzed by chiral Lewis acids.
Corey, EJ
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Dept. of Chem. and Chemical Biology, Harvard University, Cambridge
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Dept. of Chem. and Chemical Biology, Harvard University, Cambridge
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Dept. of Chem. and Chemical Biology, Harvard University, Cambridge
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[6]
SCOPE AND STEREOCHEMICAL COURSE OF THE (TRIMETHYLSILYL)CYCLOPENTENE ANNULATION
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CARINI, DJ
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FINK, DM
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FINK, DM
BASAK, A
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39
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[7]
C-2-SYMMETRIC CATIONIC COPPER(II) COMPLEXES AS CHIRAL LEWIS-ACIDS - COUNTERION EFFECTS IN THE ENANTIOSELECTIVE DIELS-ALDER REACTION
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Department of Chemistry, Harvard University, Cambridge, Massachusetts
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Department of Chemistry, Harvard University, Cambridge, Massachusetts
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Department of Chemistry, Harvard University, Cambridge, Massachusetts
VONMATT, P
NORCROSS, RD
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0
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Department of Chemistry, Harvard University, Cambridge, Massachusetts
NORCROSS, RD
MILLER, SJ
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0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge, Massachusetts
MILLER, SJ
[J].
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH,
1995,
34
(07):
: 798
-
800
[8]
MECHANISM OF THE 1,3-SIGMATROPIC SHIFT OF 2-VINYLCYCLOBUTANOL ALKOXIDES
HARRIS, NJ
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0
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0
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0
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Department of Chemistry, Indiana University, Bloomington
HARRIS, NJ
GAJEWSKI, JJ
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0
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0
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Department of Chemistry, Indiana University, Bloomington
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[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
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: 6121
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6129
[9]
A novel chiral super-Lewis acidic catalyst for enantioselective synthesis
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HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138
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机构:
HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138
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[J].
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A new powerful and practical BLA catalyst for highly enantioselective Diels-Alder reaction: An extreme acceleration of reaction rate by Bronsted acid
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Ishihara, K
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h-index:
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机构:
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
Kurihara, H
Yamamoto, H
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引用数:
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h-index:
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机构:
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
Yamamoto, H
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1996,
118
(12)
: 3049
-
3050
←
1
2
→
共 11 条
[1]
Copper-mediated cross-coupling of organostannanes with organic iodides at or below room temperature
Allred, GD
论文数:
0
引用数:
0
h-index:
0
机构:
EMORY UNIV,SANFORD S ATWOOD CHEM CTR,ATLANTA,GA 30322
EMORY UNIV,SANFORD S ATWOOD CHEM CTR,ATLANTA,GA 30322
Allred, GD
Liebeskind, LS
论文数:
0
引用数:
0
h-index:
0
机构:
EMORY UNIV,SANFORD S ATWOOD CHEM CTR,ATLANTA,GA 30322
EMORY UNIV,SANFORD S ATWOOD CHEM CTR,ATLANTA,GA 30322
Liebeskind, LS
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1996,
118
(11)
: 2748
-
2749
[2]
DEMONSTRATION OF THE SYNTHETIC POWER OF OXAZABOROLIDINE-CATALYZED ENANTIOSELECTIVE DIELS-ALDER REACTIONS BY VERY EFFICIENT ROUTES TO CASSIOL AND GIBBERELLIC-ACID
COREY, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University Cambridge, Massachusetts
COREY, EJ
GUZMANPEREZ, A
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University Cambridge, Massachusetts
GUZMANPEREZ, A
LOH, TP
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University Cambridge, Massachusetts
LOH, TP
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1994,
116
(08)
: 3611
-
3612
[3]
ENANTIOSELECTIVE TOTAL SYNTHESIS OF GRACILIN-B AND GRACILIN-C USING CATALYTIC ASYMMETRIC DIELS-ALDER METHODOLOGY
COREY, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge
COREY, EJ
LETAVIC, MA
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge
LETAVIC, MA
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1995,
117
(37)
: 9616
-
9617
[4]
THE ORIGIN OF GREATER THAN 200/1 ENANTIOSELECTIVITY IN A CATALYTIC DIELS-ALDER REACTION AS REVEALED BY PHYSICAL AND CHEMICAL STUDIES
COREY, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge
COREY, EJ
LOH, TP
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge
LOH, TP
ROPER, TD
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge
ROPER, TD
AZIMIOARA, MD
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge
AZIMIOARA, MD
NOE, MC
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge
NOE, MC
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1992,
114
(21)
: 8290
-
8292
[5]
The formyl C-H--O hydrogen bond as a key to transition-state organization in enantioselective allylation, aldol and Diels-Alder reactions catalyzed by chiral Lewis acids.
Corey, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
Dept. of Chem. and Chemical Biology, Harvard University, Cambridge
Corey, EJ
BarnesSeeman, D
论文数:
0
引用数:
0
h-index:
0
机构:
Dept. of Chem. and Chemical Biology, Harvard University, Cambridge
BarnesSeeman, D
Lee, TW
论文数:
0
引用数:
0
h-index:
0
机构:
Dept. of Chem. and Chemical Biology, Harvard University, Cambridge
Lee, TW
[J].
TETRAHEDRON LETTERS,
1997,
38
(10)
: 1699
-
1702
[6]
SCOPE AND STEREOCHEMICAL COURSE OF THE (TRIMETHYLSILYL)CYCLOPENTENE ANNULATION
DANHEISER, RL
论文数:
0
引用数:
0
h-index:
0
DANHEISER, RL
CARINI, DJ
论文数:
0
引用数:
0
h-index:
0
CARINI, DJ
FINK, DM
论文数:
0
引用数:
0
h-index:
0
FINK, DM
BASAK, A
论文数:
0
引用数:
0
h-index:
0
BASAK, A
[J].
TETRAHEDRON,
1983,
39
(06)
: 935
-
947
[7]
C-2-SYMMETRIC CATIONIC COPPER(II) COMPLEXES AS CHIRAL LEWIS-ACIDS - COUNTERION EFFECTS IN THE ENANTIOSELECTIVE DIELS-ALDER REACTION
EVANS, DA
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge, Massachusetts
EVANS, DA
MURRY, JA
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge, Massachusetts
MURRY, JA
VONMATT, P
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge, Massachusetts
VONMATT, P
NORCROSS, RD
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge, Massachusetts
NORCROSS, RD
MILLER, SJ
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Harvard University, Cambridge, Massachusetts
MILLER, SJ
[J].
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH,
1995,
34
(07):
: 798
-
800
[8]
MECHANISM OF THE 1,3-SIGMATROPIC SHIFT OF 2-VINYLCYCLOBUTANOL ALKOXIDES
HARRIS, NJ
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Indiana University, Bloomington
HARRIS, NJ
GAJEWSKI, JJ
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Chemistry, Indiana University, Bloomington
GAJEWSKI, JJ
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1994,
116
(14)
: 6121
-
6129
[9]
A novel chiral super-Lewis acidic catalyst for enantioselective synthesis
Hayashi, Y
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138
HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138
Hayashi, Y
Rohde, JJ
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138
HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138
Rohde, JJ
Corey, EJ
论文数:
0
引用数:
0
h-index:
0
机构:
HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138
HARVARD UNIV,DEPT CHEM,CAMBRIDGE,MA 02138
Corey, EJ
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1996,
118
(23)
: 5502
-
5503
[10]
A new powerful and practical BLA catalyst for highly enantioselective Diels-Alder reaction: An extreme acceleration of reaction rate by Bronsted acid
Ishihara, K
论文数:
0
引用数:
0
h-index:
0
机构:
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
Ishihara, K
Kurihara, H
论文数:
0
引用数:
0
h-index:
0
机构:
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
Kurihara, H
Yamamoto, H
论文数:
0
引用数:
0
h-index:
0
机构:
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
NAGOYA UNIV,SCH ENGN,CHIKUSA KU,NAGOYA,AICHI 46401,JAPAN
Yamamoto, H
[J].
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY,
1996,
118
(12)
: 3049
-
3050
←
1
2
→