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Lewis base catalysis in organic synthesis
被引:1095
作者
:
Denmark, Scott E.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Illinois, Roger Adams Lab, Urbana, IL 61801 USA
Univ Illinois, Roger Adams Lab, Urbana, IL 61801 USA
Denmark, Scott E.
[
1
]
Beutner, Gregory L.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Illinois, Roger Adams Lab, Urbana, IL 61801 USA
Univ Illinois, Roger Adams Lab, Urbana, IL 61801 USA
Beutner, Gregory L.
[
1
]
机构
:
[1]
Univ Illinois, Roger Adams Lab, Urbana, IL 61801 USA
来源
:
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
|
2008年
/ 47卷
/ 09期
关键词
:
catalysis;
donor-acceptor interactions;
electrophilic;
nucleophilic;
stereoselectivity;
D O I
:
10.1002/anie.200604943
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
The legacy of Gilbert Newton Lewis (1875-1946) pervades the lexicon of chemical bonding and reactivity. The power of his concept of donor-acceptor bonding is evident in the eponymous foundations of electron-pair acceptors (Lewis acids) and donors (Lewis bases). Lewis recognized that acids are not restricted to those substances that contain hydrogen (Brønsted acids), and helped overthrow the "modern cult of the proton". His discovery ushered in the use of Lewis acids as reagents and catalysts for organic reactions. However, in recent years, the recognition that Lewis bases can also serve in this capacity has grown enormously. Most importantly, it has become increasingly apparent that the behavior of Lewis bases as agents for promoting chemical reactions is not merely as an electronic complement of the cognate Lewis acids: in fact Lewis bases are capable of enhancing both the electrophilic and nucleophilic character of molecules to which they are bound. This diversity of behavior leads to a remarkable versatility for the catalysis of reactions by Lewis bases. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:1560 / 1638
页数:79
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Catalytic crossed Michael cycloisomerization of thioenoates:: Total synthesis of (±)-ricciocarpin A
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0
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0
h-index:
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Latvian Inst Organ Synth, LV-1006 Riga, Latvia
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Latvian Inst Organ Synth, LV-1006 Riga, Latvia
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[J].
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586
(02)
: 184
-
189
[2]
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Adams, DJ
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0
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Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
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Clark, JH
论文数:
0
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h-index:
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Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
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Heath, PA
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Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
Heath, PA
Hansen, LB
论文数:
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h-index:
0
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Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
Hansen, LB
Sanders, VC
论文数:
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h-index:
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Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
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Tavener, SJ
论文数:
0
引用数:
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h-index:
0
机构:
Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
Tavener, SJ
[J].
JOURNAL OF FLUORINE CHEMISTRY,
2000,
101
(02)
: 187
-
191
[3]
KINETIC-ANALYSIS OF THE DUAL CATALYSIS BY PROLINE IN THE ASYMMETRIC INTRAMOLECULAR ALDOL REACTION
AGAMI, C
论文数:
0
引用数:
0
h-index:
0
AGAMI, C
PUCHOT, C
论文数:
0
引用数:
0
h-index:
0
PUCHOT, C
[J].
JOURNAL OF MOLECULAR CATALYSIS,
1986,
38
(03):
: 341
-
343
[4]
IS THE MECHANISM OF THE PROLINE-CATALYZED ENANTIOSELECTIVE ALDOL REACTION RELATED TO BIOCHEMICAL PROCESSES
AGAMI, C
论文数:
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h-index:
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AGAMI, C
PUCHOT, C
论文数:
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h-index:
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PUCHOT, C
SEVESTRE, H
论文数:
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TETRAHEDRON LETTERS,
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AGAMI, C
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CNRS,INST CHIM SUBST NAT,F-91190 GIF SUR YVETTE,FRANCE
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CNRS,INST CHIM SUBST NAT,F-91190 GIF SUR YVETTE,FRANCE
PUCHOT, C
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CNRS,INST CHIM SUBST NAT,F-91190 GIF SUR YVETTE,FRANCE
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CNRS,INST CHIM SUBST NAT,F-91190 GIF SUR YVETTE,FRANCE
CNRS,INST CHIM SUBST NAT,F-91190 GIF SUR YVETTE,FRANCE
PASCARD, C
[J].
TETRAHEDRON,
1984,
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(06)
: 1031
-
1038
[6]
Agami C., 1988, B SOC CHIM FR MAY, V3, P499
[7]
Catalytic crossed Michael cycloisomerization of thioenoates:: Total synthesis of (±)-ricciocarpin A
Agapiou, K
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA
Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA
Agapiou, K
Krische, MJ
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0
h-index:
0
机构:
Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA
Univ Texas, Dept Chem & Biochem, Austin, TX 78712 USA
Krische, MJ
[J].
ORGANIC LETTERS,
2003,
5
(10)
: 1737
-
1740
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Reevaluation of the mechanism of the Baylis-Hillman reaction: Implications for asymmetric catalysis
Aggarwal, VK
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Aggarwal, VK
Fulford, SY
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Fulford, SY
Lloyd-Jones, GC
论文数:
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引用数:
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h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Lloyd-Jones, GC
[J].
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2005,
44
(11)
: 1706
-
1708
[9]
Correlation between pKa and reactivity of quinuclidine-based catalysts in the Baylis-Hillman reaction:: Discovery of quinuclidine as optimum catalyst leading to substantial enhancement of scope
Aggarwal, VK
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Aggarwal, VK
Emme, I
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Emme, I
Fulford, SY
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Fulford, SY
[J].
JOURNAL OF ORGANIC CHEMISTRY,
2003,
68
(03)
: 692
-
700
[10]
Rate acceleration of the Baylis-Hillman reaction in polar solvents (water and formamide). Dominant role of hydrogen bonding, not hydrophobic effects, is implicated
Aggarwal, VK
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Aggarwal, VK
Dean, DK
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Dean, DK
Mereu, A
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Mereu, A
Williams, R
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
Williams, R
[J].
JOURNAL OF ORGANIC CHEMISTRY,
2002,
67
(02)
: 510
-
514
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1
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