Relevant bibliographies by topics / Imidazo[1,5-a]azines

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  1. Journal articles

Academic literature on the topic 'Imidazo[1,5-a]azines'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "Imidazo[1,5-a]azines"

1

Pelletier, Guillaume, and André B. Charette. "Triflic Anhydride Mediated Synthesis of Imidazo[1,5-a]azines." Organic Letters 15, no. 9 (2013): 2290–93. http://dx.doi.org/10.1021/ol400870b.

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2

Pelletier, Guillaume, and Andre B. Charette. "ChemInform Abstract: Triflic Anhydride Mediated Synthesis of Imidazo[1,5-a]azines." ChemInform 44, no. 36 (2013): no. http://dx.doi.org/10.1002/chin.201336149.

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3

Sustac Roman, Daniela, Valentin Poiret, Guillaume Pelletier, and André B. Charette. "Direct Arylation of Imidazo[1,5-a]azines Through Ruthenium and Palladium Catalysis." European Journal of Organic Chemistry 2015, no. 1 (2014): 67–71. http://dx.doi.org/10.1002/ejoc.201403268.

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4

Sustac Roman, Daniela, Valentin Poiret, Guillaume Pelletier, and Andre B. Charette. "ChemInform Abstract: Direct Arylation of Imidazo[1,5-a]azines Through Ruthenium and Palladium Catalysis." ChemInform 46, no. 20 (2015): no. http://dx.doi.org/10.1002/chin.201520192.

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5

Sharma, Shubham, Avijit Kumar Paul, and Virender Singh. "La(OTf)3-catalysed one-pot synthesis of pyrazole tethered imidazo[1,2-a]azine derivatives and evaluation of their light emitting properties." New Journal of Chemistry 44, no. 3 (2020): 684–94. http://dx.doi.org/10.1039/c9nj05426j.

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6

Kolar, Patrik, and Miha Tišler. "A New Route to Imidazo(1,5-a)pyridines and -quinolines." Zeitschrift für Naturforschung B 46, no. 8 (1991): 1110–12. http://dx.doi.org/10.1515/znb-1991-0822.

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7

Gambouz, Khadija, Mohsine Driowya, Mohammed Loubidi, et al. "Unusual rearrangement of imidazo[1,5-a]imidazoles and imidazo[1,2-b]pyrazoles into imidazo[1,5-a]pyrimidines and pyrazolo[1,5-a]pyrimidines." RSC Advances 9, no. 50 (2019): 29051–55. http://dx.doi.org/10.1039/c9ra04609g.

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8

Chen, Li-Hsun, Chih-Hsien Kao, Sandip Dhole, et al. "Regioselective synthesis of imidazo[1,5-a]quinoxalines and methyl N-phenylbenzimidats on an ionic liquid support." RSC Advances 6, no. 80 (2016): 76123–27. http://dx.doi.org/10.1039/c6ra11861e.

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An ionic liquid supported synthesis of imidazo[1,5-a]quinoxalines and methyl N-phenylbenzimidats was explored to generate polycyclic imidazo[1,5-a]quinoxalines and methyl N-phenylbenzimidats during the cleavage of the support.
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9

Hannah, Duncan R., and Malcolm F. G. Stevens. "Structural Studies on Bioactive Compounds. Part 38.1 Reactions of 5-Aminoimidazole-4-Carboxamide: Synthesis of Imidazo[1,5-a]Quinazoline-3-Carboxamides." Journal of Chemical Research 2003, no. 7 (2003): 398–401. http://dx.doi.org/10.3184/030823403103174533.

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5-Aminoimidazole-4-carboxamide reacts with aromatic aldehydes to afford Schiff bases which can be cyclised to imidazo[1,5- a]quinazoline-3-carboxamides in DMF/sodium hydride. The potassium salt of imidazo[1,5- a]quinazoline-3-carboxylic acid undergoes deuterium exchange in D2O at the 1-position.
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10

Gad-Elkareem, Mohamed A. M., Azza M. Abdel-Fattah, and Mohamed A. A. Elneairy. "Pyrazolo[3,4-b]pyridine in heterocyclic synthesis: synthesis of new pyrazolo[3,4-b]pyridines, imidazo[1',2':1,5]pyrazolo[3,4-b]pyridines, and pyrido[2',3':3,4]pyrazolo[1,5-a]pyrimidines." Canadian Journal of Chemistry 85, no. 9 (2007): 592–99. http://dx.doi.org/10.1139/v07-089.

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Pyrazolo[3,4-b]pyridine derivatives 7 and 9 were synthesized via the reaction of 3-amino-1H-pyrazolo-[3,4-b]pyridine derivative 2 with ω-bromoacetophenones. Reaction of 7 and 9 with Ac2O afforded the imidazo[1',2':1,5]py razolo[3,4-b]pyridine derivative 8 and pyrazolo[3,4-b]pyridine derivative 10, respectively. Reaction of 2 with chloroacetonitrile followed by DMF-DMA gave imidazo[1',2':1,5]pyrazolo[3,4-b]pyridines 4 and 5, respectively. Acetyl acetone and 1,1-dicyano-2,2-dimethylthioethene were reacted with 2 to afford the pyrido[2',3':3,4]pyrazolo-[1,5-a]-pyrimidines 11 and 14, respectively.
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