Search results for "Pyrrole derivative"
showing 10 items of 44 documents
One-Pot Synthesis of Polysubstituted Pyrrolidines from Aminonitriles
2005
α-Aminonitriles with a mono- or unsubstituted amino group as well as a-(alkylideneamino)nitriles can be employed as easily accessible α-aminocarbanion equivalents. Their α-deprotonation yields stabilized carbanions, whichundergo smooth 1,4-addition to α,β-unsaturated carbonyl compounds. The resulting δ-ketoα-aminonitriles can be reductively cyclized to form polysubstituted pyrrolidines.
ChemInform Abstract: (4 + 2) Cycloaddition of Indole Derivatives with Bismaleimides: A Route to New Biscarbazoles.
2010
ChemInform Abstract: Pyrroles and Indolizidines from Deprotonated α-(Alkylideneamino)nitriles.
2011
1-Pyrrolines (3,4-Dihydro-2H-pyrroles) as a Template for New Drugs
2001
ChemInform Abstract: 4-Fluoroanilines: Synthesis and Decomposition.
2010
Abstract Fourteen N- and/or 2-substituted 4-fluoroanilines were prepared (the series includes N–C2-bridged compounds). Some of them were found to be thermally unstable when dissolved in chloroform. Both 19 F NMR spectra and comparison of GIAO-DFT calculated and experimental 13 C chemical shifts were used to suggest decomposition products of 4-fluoroanilines.
SYNTHESIS OF NEW OLIGOPEPTIDE PYRROLE DERIVATIVES
2008
Synthesis of the new oligopeptide pyrrole derivative isonetropsin and its one pyrrole unit analogue
2013
We have designed and synthesized isonetropsin and its one pyrrole unit analogue in which the amine and carbonyl groups have been switched in positions 2 and 4, respectively instead of 4 and 2 positions of the natural antibiotic netropsin.
Structural Approaches to Explain the Selectivity of COX-2 Inhibitors: Is There a Common Pharmacophore?
2000
The identification and characterisation of the isoenzyme cyclooxygenase 2 (COX-2) stimulated investigations to develop efficient non-steroidal anti-inflammatory drugs with reduced side effects compared to standard NSAIDs. This review will focus on the structural features needed to achieve COX-2 selectivity. Five structural classes can be identified together with a class bearing little or no resemblance to one another in their molecular structure. The most interesting point is the very distinct structure/activity relationship. On the one hand only minor modifications to a particular compound induce a drastic change in its COX selectivity and on the other hand the structural prerequisites in …
ChemInform Abstract: Synthesis of Five-Membered Nitrogen Heterocycles from Iron-Substituted Enals: Novel Insight into the η5-Cyclopentadienyl(dicarbo…
2010
Novel bioactive bromopyrrole alkaloids from the Mediterranean sponge Axinella verrucosa
2005
The Mediterranean sponge Axinella verrucosa has been investigated for its alkaloid composition and has been found to produce a complex mixture of bromopyrrole alkaloids. Along with the previously isolated compounds 5-18, four novel alkaloids of this class, compounds 1-4, have been isolated, and their structures established through spectroscopic methods. Compounds 1-4 were found to display neuroprotective activity against the agonists serotonin and glutamate in vitro.