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pyrrolidine
National Institutes of Health
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Related topics
Related topics
9 relations
Broader (3)
Heterocyclic Compounds, 1-Ring
Pyrrolidines
nitrogenous heterocyclic compound
Narrower (5)
Kainate
Pyrrolidinones
dipyrrolidine
pyrrolidine hydrochloride
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Nafoxidine
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2018
Review
2018
Application of 1,3‐Dipolar Reactions between Azomethine Ylides and Alkenes to the Synthesis of Catalysts and Biologically Active Compounds
Iosune Arrastia
,
A. Arrieta
,
F. Cossío
European journal of organic chemistry
2018
Corpus ID: 56476980
The (3+2) cycloaddition between azomethine ylides and alkenes is an efficient, convergent and stereocontrolled method for the…
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Highly Cited
2010
Highly Cited
2010
CHARMM general force field: A force field for drug‐like molecules compatible with the CHARMM all‐atom additive biological force fields
K. Vanommeslaeghe
,
Elizabeth Hatcher
,
+8 authors
Alexander D. MacKerell
J. Comput. Chem.
2010
Corpus ID: 17193482
The widely used CHARMM additive all‐atom force field includes parameters for proteins, nucleic acids, lipids, and carbohydrates…
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Highly Cited
2010
Highly Cited
2010
Pyrrolidine constrained bipyridyl-dansyl click fluoroionophore as selective Al(3+)sensor.
D. Maity
,
T. Govindaraju
Chemical communications
2010
Corpus ID: 31982773
A pyrrolidine constrained bipyridyl-dansyl (ionophore-fluorophore) conjugate with triazole linker was synthesised through click…
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Highly Cited
2007
Highly Cited
2007
Enantioselective construction of spirocyclic oxindolic cyclopentanes by palladium-catalyzed trimethylenemethane-[3+2]-cycloaddition.
B. Trost
,
N. Cramer
,
S. M. Silverman
Journal of the American Chemical Society
2007
Corpus ID: 207045173
The palladium catalyzed [3+2] trimethylenemethane (TMM) cycloaddition is an efficient method for the construction of…
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Highly Cited
2007
Highly Cited
2007
Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions.
S. S. V. Ramasastry
,
Haile Zhang
,
F. Tanaka
,
C. Barbas
Journal of the American Chemical Society
2007
Corpus ID: 9742264
Chiral 1,2-amino alcohols and 1,2-diols are common structural motifs found in a vast array of natural and biologically active…
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Highly Cited
2006
Highly Cited
2006
Construction of enantiopure pyrrolidine ring system via asymmetric [3+2]-cycloaddition of azomethine ylides.
G. Pandey
,
P. Banerjee
,
S. Gadre
Chemical reviews
2006
Corpus ID: 38579968
Highly Cited
2004
Highly Cited
2004
A new class of chiral pyrrolidine-pyridine conjugate base catalysts for use in asymmetric Michael addition reactions.
T. Ishii
,
Shingo Fujioka
,
Y. Sekiguchi
,
H. Kotsuki
Journal of the American Chemical Society
2004
Corpus ID: 42800214
Direct catalytic asymmetric Michael addition reactions of ketones to nitroolefins using newly developed chiral pyrrolidine…
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Highly Cited
2003
Highly Cited
2003
Interactions of Peroxynitrite, Tetrahydrobiopterin, Ascorbic Acid, and Thiols
Nermin Kuzkaya
,
N. Weissmann
,
D. Harrison
,
S. Dikalov
Journal of Biological Chemistry
2003
Corpus ID: 28707243
Tetrahydrobiopterin (BH4) serves as a critical co-factor for the endothelial nitric-oxide synthase (eNOS). A deficiency of BH4…
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Highly Cited
1992
Highly Cited
1992
Dithiocarbamates as potent inhibitors of nuclear factor kappa B activation in intact cells
R. Schreck
,
B. Meier
,
D. Männel
,
W. Droege
,
P. Baeuerle
The Journal of experimental medicine
1992
Corpus ID: 6226786
Dithiocarbamates and iron chelators were recently considered for the treatment of AIDS and neurodegenerative diseases. In this…
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Highly Cited
1990
Highly Cited
1990
Receptor-coupled signal transduction in human polymorphonuclear neutrophils: effects of a novel inhibitor of phospholipase C-dependent processes on cell responsiveness.
R. Smith
,
L. Sam
,
J. M. Justen
,
G. Bundy
,
G. Bala
,
J. Bleasdale
The Journal of pharmacology and experimental…
1990
Corpus ID: 45756383
1-[6-[[17 beta-3-Methoxyestra-1,3,5(10)-trien-17-yl]amino]hexyl]- 1H-pyrrole-2,5-dione (U-73122), an inhibitor of phospholipase C…
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