Paper
Condensation of 1,4-diacetylpiperazine-2,5-dione with aldehydes
Published 1974 · C. Gallina, A. Liberatori
Tetrahedron
Q3 SJR score
58
Citations
1
Influential Citations
Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
Study Snapshot
This study successfully synthesized albonoursin and unsymmetrical 3,6-diarylidenepiperazine-2,5-diones using 1,4-diacetylpiperazine-2,5-dione and aldehydes, with a focus on mechanism and stereochemistry.
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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References
Activation of the amide group by acylation hydroxy- and aminoacyl incorporation in peptide systems.
This new reaction allows for the synthesis of linear or cyclic peptides and depsipeptides, with potential applications in antibiotic synthesis.
1965·71citations·M. M. Shemyakin et al.·Tetrahedron
Tetrahedron
Citations
New Quinoid Bio-Inspired Materials Using Para-Azaquinodimethane Moiety
Bio-inspired quinoid materials containing para-azaquinodimethane (p-AQM) moiety show promising properties for optoelectronic applications and high thermal stabilities, making them potential candidates for electronic or biomedical applications.
2023·1citation·Walaa Zwaihed et al.·Molecules
Molecules
A highly substituted pyrazinophane generated from a quinoidal system via a cascade reaction.
This study demonstrates the generation of a highly-substituted pyrazinophane via a cascade reaction, shedding light on the stability of p-AQMs and analyzing its electronic and structural properties.
2020·6citations·Christopher L. Anderson et al.·Chemical communications
Chemical communications
Electronic Tuning of Mixed Quinoidal-Aromatic Conjugated Polyelectrolytes via Direct Ionic Substitution.
Direct ionic substitution enables the synthesis of ionic azaquinodimethane compounds, offering tunable optical properties and potential applications in photothermal therapy.
2019·11citations·Christopher L. Anderson et al.·Angewandte Chemie
Angewandte Chemie
Electronic Tuning of Mixed Quinoidal‐Aromatic Conjugated Polyelectrolytes: Direct Ionic Substitution on Polymer Main‐Chains
Direct ionic substitution on polymer main chains can effectively tune the energetics of mixed quinoidal-aromatic conjugated polyelectrolytes, resulting in functional ionic semiconductors with desirable optoelectronic properties.
2019·19citations·Christopher L. Anderson et al.·Angewandte Chemie
Angewandte Chemie
Heterocyclic cellular lipid peroxidation inhibitors inspired by the marine antioxidant barettin.
A library of synthetic compounds based on marine antioxidant barettin showed superior antioxidant properties and no toxicity against MRC-5 lung fibroblasts.
2019·10citations·Christophe Labrière et al.·Bioorganic chemistry
Bioorganic chemistry
Development and evaluation of cationic amphiphilic antimicrobial 2,5‐diketopiperazines
Cyclic cationic amphiphilic peptidomimetics show potential as promising compounds for treating infections caused by microorganisms with increased resistance to conventional antimicrobial agents.
2018·14citations·Christophe Labrière et al.·Journal of Peptide Science
Journal of Peptide Science
para-Azaquinodimethane: A Compact Quinodimethane Variant as an Ambient Stable Building Block for High-Performance Low Band Gap Polymers.
The stable p-azaquinodimethane (p-AQM) unit offers a promising building block for high-performance low band gap polymers with promising optical and electronic properties.
2017·53citations·Xuncheng Liu et al.·Journal of the American Chemical Society
Journal of the American Chemical Society
Site selective synthesis of cytotoxic 1,3,6-trisubstituted 3,6-diunsaturated (3Z,6Z)-2,5-diketopiperazines via a one-pot multicomponent method
A one-pot multicomponent method allows for the selective synthesis of cytotoxic 1,3,6-trisubstituted 3,6-diunsaturated (3Z,6Z)-2,5-diketopiperazine derivatives with high stereoselectivity, potentially resulting in a drug
2016·10citations·Shengrong Liao et al.·Tetrahedron
Tetrahedron