pyrrole-2-carboxaldehyde

Known as: pyrrole-2-carbaldehyde 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1986-2018
024619862018

Papers overview

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2017
2017
The interaction of external water molecules with hydrated pyrrole-2-carboxaldehyde PCL/(H2O) n complexes was investigated. The… (More)
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2012
2012
Toward the expansion of the genetic alphabet, an unnatural base pair between 7-(2-thienyl)imidazo[4,5-b]pyridine (Ds) and pyrrole… (More)
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2010
2010
Methods for fluorescent probing at a defined position of RNA provide powerful tools for analyzing the local structural… (More)
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2010
2010
The expansion of the genetic alphabet, by an unnatural base pair system, provides a powerful tool for the site-specific… (More)
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2008
2008
An unnatural base pair between 7-(2-thienyl)-imidazo[4,5-b]pyridine (Ds) and pyrrole-2-carbaldehyde (Pa) could expand the genetic… (More)
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2007
2007
Intermolecular interactions relevant for antiparallel beta-sheet formation between peptide strands are studied by Fourier… (More)
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2007
2007
Expansion of the genetic alphabet by an unnatural base pair system provides a powerful tool for modern biotechnology. As an… (More)
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2005
2005
Copper complexes of thiosemicarbazones of imidazole-2-carbaldehyde, pyrrole-2-carbaldehyde and indole-3-carbaldehyde were… (More)
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2003
2003
An unnatural hydrophobic base, pyrrole-2-carbaldehyde (denoted as Pa), was developed as a specific pairing partner of 9… (More)
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2003
2003
To develop unnatural base pairs that function in replication, we designed 4-propynylpyrrole-2-carbaldehyde (designated as Pa… (More)
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