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Lewis Bases
Known as:
Bases, Lewis
, Lewis Bases [Chemical/Ingredient]
, Lewis base
Any chemical species which acts as an electron-pair donor in a chemical bonding reaction with a LEWIS ACID.
National Institutes of Health
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8 relations
Broader (1)
Base
In Blood
agonists
analogs & derivatives
antagonists & inhibitors
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Highly Cited
2013
Highly Cited
2013
Catalytic [4+2] cyclization of α,β-unsaturated acyl chlorides with 3-alkylenyloxindoles: highly diastereo- and enantioselective synthesis of spirocarbocyclic oxindoles.
Lichun Shen
,
Wen‐Qiang Jia
,
Song Ye
Angewandte Chemie
2013
Corpus ID: 29078278
Cinchona alkaloids were used as Lewis base catalysts in the title reaction. The [4+2] cyclization of α,β-unsaturated acyl…
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Highly Cited
2012
Highly Cited
2012
Differential sensing of Zn(II) and Cu(II) via two independent mechanisms.
Prem N. Basa
,
Andrew G Sykes
Journal of Organic Chemistry
2012
Corpus ID: 7228733
Selective reduction of an anthracenone-quinoline imine derivative, 2, using 1.0 equiv of NaBH(4) in 95% ethanol affords the…
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Highly Cited
2008
Highly Cited
2008
Planar, twisted, and trans-bent: conformational flexibility of neutral diborenes.
Yuzhong Wang
,
B. Quillian
,
+6 authors
G. Robinson
Journal of the American Chemical Society
2008
Corpus ID: 207121998
The potassium graphite reduction of R‘BBr3 (R‘ = :C{N(2,4,6-Me3C6H2)CH}2) in Et2O led to the isolation of 3 (R‘(H)BB(H)R‘) and 4…
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Highly Cited
2008
Highly Cited
2008
Highly enantioselective synthesis of beta-amino acid derivatives by the lewis base catalyzed hydrosilylation of beta-enamino esters.
Hong‐Jie Zheng
,
Wenbin Chen
,
+4 authors
Xiaomei Zhang
Chemistry
2008
Corpus ID: 21517540
Highly Cited
2007
Highly Cited
2007
Functionalization and solubilization of BN nanotubes by interaction with Lewis bases
S. Pal
,
S. Vivekchand
,
A. Govindaraj
,
C. Rao
2007
Corpus ID: 53473777
By interaction with a trialkylamine or trialkylphosphine, BN nanotubes can be dispersed in a hydrocarbon medium with retention of…
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Highly Cited
2005
Highly Cited
2005
Bifunctional organocatalysts for enantioselective aza-Morita-Baylis-Hillman reaction.
Katsuya Matsui
,
S. Takizawa
,
H. Sasai
Journal of the American Chemical Society
2005
Corpus ID: 37684813
The efficient and novel bifunctional organocatalyst for the enantioselective aza-Morita-Baylis-Hillman (aza-MBH) reaction has…
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Highly Cited
2005
Highly Cited
2005
Lewis base catalyzed, enantioselective aldol addition of methyl trichlorosilyl ketene acetal to ketones.
S. Denmark
,
Yu Fan
,
Martin D. Eastgate
Journal of Organic Chemistry
2005
Corpus ID: 45585789
The catalytic enantioselective addition of an acetate enolate equivalent to ketones is described. Methyl trichlorosilyl ketene…
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Highly Cited
2003
Highly Cited
2003
Chiral phosphine Lewis base catalyzed asymmetric aza-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone and phenyl acrylate.
M. Shi
,
Lian Chen
Chemical Communications
2003
Corpus ID: 11437031
In the aza-Baylis-Hillman reaction of N-sulfonated imines with methyl vinyl ketone (MVK) promoted by chiral phosphine Lewis base…
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Highly Cited
2003
Highly Cited
2003
Carbon dioxide/epoxide coupling reactions utilizing Lewis base adducts of zinc halides as catalysts. Cyclic carbonate versus polycarbonate production.
D. Darensbourg
,
S. Lewis
,
Jody L. Rodgers
,
J. C. Yarbrough
Inorganic Chemistry
2003
Corpus ID: 6428965
The reactions of zinc halides with 2,6-di-methoxypyridine or 3-trifluoromethylpyridine in dichloromethane have led to the…
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Review
2002
Review
2002
Recent progress in asymmetric two-center catalysis.
M. Shibasaki
,
M. Kanai
,
K. Funabashi
Chemical Communications
2002
Corpus ID: 9262496
Recent progress using two types of enantioselective two-center catalysts, Lewis acid-Brönsted base and Lewis acid-Lewis base…
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