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Chirality (chemistry)
Known as:
Chiral compounds
, Right-handed protein
, L-form
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Chirality /kaɪˈrælɪti/ is a geometric property of some molecules and ions. A chiral molecule/ion is non-superposable on its mirror image. The…
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Related topics
Related topics
19 relations
Chirality (mathematics)
Circular dichroism
Circular polarization
CoNTub
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Broader (1)
Polarization (waves)
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2004
Highly Cited
2004
Monolithic Integration of Carbon Nanotube Devices with Silicon MOS Technology
Yu-Chih Tseng
,
Peiqi Xuan
,
+4 authors
H. Dai
2004
Corpus ID: 1560670
An integrated circuit combining single-walled carbon nanotube (SWNT) devices with n-channel metal oxide semiconductor (NMOS…
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Highly Cited
1998
Highly Cited
1998
An unprecedented triply interpenetrated chiral network of ‘square-planar’ metal centres from the self-assembly of copper(II) nitrate and 1,2-bis(4-pyridyl)ethyne
L. Carlucci
,
G. Ciani
,
P. Macchi
,
D. Proserpio
1998
Corpus ID: 56213181
Copper(II) nitrate reacts with 1,2-bis(4-pyridyl)ethyne (bpethy) in ethanol to yield mixtures containing, beside to a one…
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Highly Cited
1997
Highly Cited
1997
C2-SYMMETRIC COPPER(II) COMPLEXES AS CHIRAL LEWIS ACIDS. CATALYTIC ENANTIOSELECTIVE ALDOL ADDITIONS OF ENOLSILANES TO PYRUVATE ESTERS
D. A. Evans
,
M. Kozlowski
,
and Christopher S. Burgey
,
D. MacMillan
1997
Corpus ID: 97470578
Our laboratory has been engaged in the development of chiral Cu(II)-based Lewis acids that exhibit the capacity to catalyze…
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Highly Cited
1996
Highly Cited
1996
C2-Symmetric Copper(II) Complexes as Chiral Lewis Acids. Catalytic Enantioselective Aldol Additions of Silylketene Acetals to (Benzyloxy)acetaldehyde
D. A. Evans
,
J. Murry
,
M. Kozlowski
1996
Corpus ID: 94418814
The Lewis acid-catalyzed addition of enolsilanes to aldehydes, commonly known as the Mukaiyama aldol reaction, 1,2 is an…
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Review
1986
Review
1986
Improved cyclodextrin chiral phases: a comparison and review
T. Ward
,
D. Armstrong
1986
Corpus ID: 205485998
Abstract Cyclodextrin chiral phases have been shown to be widely applicable for the separation of enantiomers, diastereomers…
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Highly Cited
1986
Highly Cited
1986
Stereoselective amination of chiral enolates. A new approach to the asymmetric synthesis of .alpha.-hydrazino and .alpha.-amino acid derivatives
D. A. Evans
,
T. Britton
,
R. L. Dorow
,
J. Dellaria
1986
Corpus ID: 95787111
L'«amination» electrophile d'enolates chiraux derives d'acyl-3 oxazolidones par l'azoformiate de di-t-butyle permet la synthese d…
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Highly Cited
1985
Highly Cited
1985
The asymmetric synthesis of β-lactam antibiotics - I. application of chiral oxazolidones in the staudinger reaction.
D. A. Evans
,
E. Sjogren
1985
Corpus ID: 97481854
Highly Cited
1981
Highly Cited
1981
Model Calculations of Potential Surfaces of van der Waals Complexes Containing Large Aromatic Molecules
M. Ondrechen
,
Z. Berkovitch-yellin
,
J. Jortner
1981
Corpus ID: 59154798
In this paper we report the results of model calculations of the nuclear potential surfaces of van der Waals complexes consisting…
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Highly Cited
1981
Highly Cited
1981
Enantioselective alkylation of chiral enolates
D. A. Evans
,
J. M. Takacs
1981
Corpus ID: 93924696
Highly Cited
1980
Highly Cited
1980
Total synthesis of (R)-glycerol acetonide and the antiepileptic and hypotensive drug (-)-gamma-amino-beta-hydroxybutyric acid (GABOB): use of vitamin C as a chiral starting material
M. Jung
,
T. Shaw
1980
Corpus ID: 4985321
Ascorbic acid (Vitamin C) (9) is shown to be a useful, inexpensive chiral starting material for natural products synthesis. It is…
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