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pyrrolidine

 
National Institutes of Health

Related topics

Related topics

9 relations

Broader (3)

Heterocyclic Compounds, 1-RingPyrrolidinesnitrogenous heterocyclic compound

Narrower (5)

KainatePyrrolidinonesdipyrrolidinepyrrolidine 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
The (3+2) cycloaddition between azomethine ylides and alkenes is an efficient, convergent and stereocontrolled method for the… Expand
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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
The widely used CHARMM additive all‐atom force field includes parameters for proteins, nucleic acids, lipids, and carbohydrates… Expand
Highly Cited
2010
Highly Cited
2010
Pyrrolidine constrained bipyridyl-dansyl click fluoroionophore as selective Al(3+)sensor.
A pyrrolidine constrained bipyridyl-dansyl (ionophore-fluorophore) conjugate with triazole linker was synthesised through click… Expand
Highly Cited
2007
Highly Cited
2007
Enantioselective construction of spirocyclic oxindolic cyclopentanes by palladium-catalyzed trimethylenemethane-[3+2]-cycloaddition.
The palladium catalyzed [3+2] trimethylenemethane (TMM) cycloaddition is an efficient method for the construction of… Expand
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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.
Chiral 1,2-amino alcohols and 1,2-diols are common structural motifs found in a vast array of natural and biologically active… Expand
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Highly Cited
2006
Highly Cited
2006
Construction of enantiopure pyrrolidine ring system via asymmetric [3+2]-cycloaddition of azomethine ylides.
 
Highly Cited
2004
Highly Cited
2004
A new class of chiral pyrrolidine-pyridine conjugate base catalysts for use in asymmetric Michael addition reactions.
Direct catalytic asymmetric Michael addition reactions of ketones to nitroolefins using newly developed chiral pyrrolidine… Expand
Highly Cited
2003
Highly Cited
2003
Interactions of Peroxynitrite, Tetrahydrobiopterin, Ascorbic Acid, and Thiols
Tetrahydrobiopterin (BH4) serves as a critical co-factor for the endothelial nitric-oxide synthase (eNOS). A deficiency of BH4… Expand
Highly Cited
1992
Highly Cited
1992
Dithiocarbamates as potent inhibitors of nuclear factor kappa B activation in intact cells
Dithiocarbamates and iron chelators were recently considered for the treatment of AIDS and neurodegenerative diseases. In this… Expand
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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.
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… Expand
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