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One‐pot synthesis of 1,3‐disubstituted imidazo[1,5‐a]pyridines via acceptorless dehydrogenative coupling of primary alcohols promoted by binuclear ruthenium(II) N^O‐chelating complexes
Applied Organometallic Chemistry,
2023
DOI:10.1002/aoc.6986
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[2]
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Luminescent Imidazo[1,5‐a]pyridine Scaffold: Synthetic Heterocyclization Strategies‐Overview and Promising Applications
Asian Journal of Organic Chemistry,
2022
DOI:10.1002/ajoc.202200171
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[3]
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Recent synthetic methodologies for imidazo[1,5-a]pyridines and related heterocycles
Organic & Biomolecular Chemistry,
2022
DOI:10.1039/D2OB00386D
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[4]
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Luminescent Imidazo[1,5‐
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Asian Journal of Organic Chemistry,
2022
DOI:10.1002/ajoc.202200171
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[5]
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Imidazo[1,5-a]pyridine derivatives: useful, luminescent and versatile scaffolds for different applications
New Journal of Chemistry,
2021
DOI:10.1039/D1NJ00322D
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[6]
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Synthesis of 1,3‐Disubstituted Imidazo[1,5‐a]pyridines through Oxidative C‐N Bond Formation from Aryl‐2‐pyridylmethanols and Their Fluorescent Study
ChemistrySelect,
2019
DOI:10.1002/slct.201901440
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[7]
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Multicomponent Reaction for Synthesis of Novel 2‐Tosyloxyphenylpyridines
Journal of Heterocyclic Chemistry,
2019
DOI:10.1002/jhet.3521
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[8]
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Coordination geometry-induced optical imaging of l-cysteine in cancer cells using imidazopyridine-based copper(ii) complexes
Dalton Transactions,
2019
DOI:10.1039/C8DT04634D
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[9]
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Multicomponent Reaction for Synthesis of Novel 2-Tosyloxyphenylpyridines
Journal of Heterocyclic Chemistry,
2019
DOI:10.1002/jhet.3521
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[10]
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Synthesis of 1,3‐Disubstituted Imidazo[1,5‐
a
]pyridines through Oxidative C‐N Bond Formation from Aryl‐2‐pyridylmethanols and Their Fluorescent Study
ChemistrySelect,
2019
DOI:10.1002/slct.201901440
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[11]
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Solvent-free microwave-assisted synthesis of imidazo[1,5- a]pyridine and –quinoline derivatives
Synthetic Communications,
2019
DOI:10.1080/00397911.2019.1650188
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[12]
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Tuning ‘Stokes Shift’ and ICT Character by Varying the Donor Group in Imidazo[1,5 a]pyridines: A Combined Optical, DFT, TD‐DFT and NLO Approach
ChemistrySelect,
2018
DOI:10.1002/slct.201702579
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[13]
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Tuning ‘Stokes Shift’ and ICT Character by Varying the Donor Group in Imidazo[1,5 a]pyridines: A Combined Optical, DFT, TD-DFT and NLO Approach
ChemistrySelect,
2018
DOI:10.1002/slct.201702579
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[14]
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Facile synthesis of novel blue light and large Stoke shift emitting tetradentate polyazines based on imidazo[1,5- a ]pyridine – Part 2
Dyes and Pigments,
2017
DOI:10.1016/j.dyepig.2017.04.034
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[15]
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A Simple and Ecofriendly One‐Pot Synthesis of Highly Substituted 3‐Cyanopyridine‐Quinoline Hybrids via a Triphenyphosphine‐Catalyzed Multicomponent Reaction Under Mild Conditions
Journal of Heterocyclic Chemistry,
2017
DOI:10.1002/jhet.2631
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[16]
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A Simple and Ecofriendly One-Pot Synthesis of Highly Substituted 3-Cyanopyridine-Quinoline Hybridsviaa Triphenyphosphine-Catalyzed Multicomponent Reaction Under Mild Conditions
Journal of Heterocyclic Chemistry,
2017
DOI:10.1002/jhet.2631
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[17]
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One pot synthesis of low cost emitters with large Stokes' shift
Dyes and Pigments,
2017
DOI:10.1016/j.dyepig.2016.09.056
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[18]
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Facile synthesis of novel blue light and large Stoke shift emitting tetradentate polyazines based on imidazo[1,5-a]pyridine
Dyes and Pigments,
2016
DOI:10.1016/j.dyepig.2015.12.005
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[19]
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Synthesis of Fused Five-MemberedN,N-Heterocycles Using Microwave Irradiation
Synthetic Communications,
2015
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[20]
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Synthesis and Characterization of Boron Complexes of Imidazo[1,5-a]pyridylalkyl Alcohols
Chemistry Letters,
2013
DOI:10.1246/cl.130274
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[21]
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Synthesis and Characterization of Boron Complexes of Imidazo[1,5-a]pyridylalkyl Alcohols
Chemistry Letters,
2013
DOI:10.1246/cl.130274
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[22]
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Imidazo[1,5-a]pyridine-1-ylalkylalcohols: synthesis via intramolecular cyclization of N-thioacyl 1,2-aminoalcohols and their silyl ethers and molecular structures
Organic & Biomolecular Chemistry,
2012
DOI:10.1039/c2ob25438g
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