Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,077,366 papers from all fields of science
Search
Sign In
Create Free Account
Quinolines
Known as:
1 benzazine
, Quinolines [Chemical/Ingredient]
, quinoline
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
50 relations
Narrower (49)
2-(trichloromethyl)quinoline
2-acrylamidoquinoline
2-phenylquinoline
3-hydroxyquinoline-2-carboxamide
Expand
antagonists & inhibitors
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2012
Review
2012
A walk around the A3-coupling.
Vsevolod A. Peshkov
,
Olga P. Pereshivko
,
E. V. Van der Eycken
Chemical Society Reviews
2012
Corpus ID: 9322640
In recent years, the transition-metal catalyzed three-component coupling of an aldehyde, an alkyne and an amine, commonly called…
Expand
Review
2011
Review
2011
Quinoline as a privileged scaffold in cancer drug discovery.
Solomon Vr
,
H. Lee
Current Medicinal Chemistry
2011
Corpus ID: 23509287
Quinoline (1-azanaphthalene) is a heterocyclic aromatic nitrogen compound characterized by a double-ring structure that contains…
Expand
Highly Cited
2008
Highly Cited
2008
Rh(I)-catalyzed direct arylation of pyridines and quinolines.
A. M. Berman
,
Jared C. Lewis
,
R. Bergman
,
J. Ellman
Journal of the American Chemical Society
2008
Corpus ID: 197048553
A Rh(I)-catalyzed direct arylation of pyridine and quinoline heterocycles has been developed. The method provides rapid entry…
Expand
Highly Cited
2006
Highly Cited
2006
New insights into the antiviral effects of chloroquine
A. Savarino
,
L. di Trani
,
I. Donatelli
,
R. Cauda
,
Antonio Cassone
Lancet. Infectious Diseases (Print)
2006
Corpus ID: 42283467
Highly Cited
2006
Highly Cited
2006
A highly enantioselective Brønsted acid catalyzed cascade reaction: organocatalytic transfer hydrogenation of quinolines and their application in the synthesis of alkaloids.
M. Rueping
,
A. Antonchick
,
Thomas Theissmann
Angewandte Chemie
2006
Corpus ID: 86875
The enantioselective hydrogenation of olefins, ketones, and imines still represents an important topic in organic synthesis and…
Expand
Highly Cited
2006
Highly Cited
2006
Asymmetric hydrogenation of quinolines and isoquinolines activated by chloroformates.
Shenglin Lu
,
You-Qing Wang
,
Xiuwen Han
,
Yong‐Gui Zhou
Angewandte Chemie
2006
Corpus ID: 30379584
Despite significant progress in the area of asymmetric hydrogenation, the enantioselective hydrogenation of aromatic and…
Expand
Highly Cited
2003
Highly Cited
2003
Highly enantioselective iridium-catalyzed hydrogenation of heteroaromatic compounds, quinolines.
Wen-Bo Wang
,
Shenglin Lu
,
Peng Yang
,
Xiuwen Han
,
Yong‐Gui Zhou
Journal of the American Chemical Society
2003
Corpus ID: 46210354
The highly enantioselective hydrogenation of quinoline derivatives is developed using [Ir(COD)Cl]2/(R)-MeO-Biphep/I2 system, and…
Expand
Highly Cited
1994
Highly Cited
1994
A new series of PDGF receptor tyrosine kinase inhibitors: 3-substituted quinoline derivatives.
M. Maguire
,
Kimberly R. Sheets
,
K. McVety
,
A. Spada
,
A. Zilberstein
Journal of Medicinal Chemistry
1994
Corpus ID: 27082474
A series of 63 3-substituted quinoline derivatives has been prepared and tested for inhibition of cell-free platelet derived…
Expand
Highly Cited
1989
Highly Cited
1989
Magnetic field effects in chemical kinetics and related phenomena
U. Steiner
,
T. Ulrich
1989
Corpus ID: 95076155
ions was studied by Margulis et al.156 These authors used solvent mixtures of water or ethanol with glycerol to obtain very…
Expand
Highly Cited
1980
Highly Cited
1980
New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures.
R. Tsien
Biochemistry
1980
Corpus ID: 19043852
A new family of high-affinity buffers and optical indicators for Ca2+ is rationally designed and synthesized. The parent compound…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE