Relevant bibliographies by topics / DABAL-Me3

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'DABAL-Me3'

Author: Grafiati
Published: 21 February 2023

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Journal articles on the topic "DABAL-Me3"

1

Goswami, Abhishek. "DABAL-Me3: A Versatile Methylating Agent." Synlett 2009, no. 13 (2009): 2203–4. http://dx.doi.org/10.1055/s-0029-1217623.

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Dubois, Nathalie, Daniel Glynn, Thomas McInally, et al. "On DABAL-Me3 promoted formation of amides." Tetrahedron 69, no. 46 (2013): 9890–97. http://dx.doi.org/10.1016/j.tet.2013.08.062.

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Glynn, Daniel, David Bernier, and Simon Woodward. "Microwave acceleration in DABAL-Me3-mediated amide formation." Tetrahedron Letters 49, no. 39 (2008): 5687–88. http://dx.doi.org/10.1016/j.tetlet.2008.07.090.

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4

Jeong, Byung-Hoon, Hee-Kwon Kim, and David H. Thompson. "A Facile and Efficient Method for the Formation of Unsymmetrical Ureas Using DABAL-Me3." Australian Journal of Chemistry 69, no. 7 (2016): 805. http://dx.doi.org/10.1071/ch15675.

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A practical synthetic method for the formation of unsymmetrical-substituted ureas is described. The synthesis of the unsymmetrical ureas was readily performed from 2,2,2-trichloroethyl carbamate compounds by treatment of amines with bis(trimethylaluminum)-1,4-diazabicyclo[2.2.2]octane (DABAL-Me3). Using this reaction protocol, various trisubstituted and tetrasubstituted ureas were synthesized in high yields. This study offers a promising approach for the facile synthesis of a variety of unsymmetrical ureas from 2,2,2-trichloroethyl carbamates.
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Cooper, Thea, Andrew Novak, Luke D Humphreys, Matthew D Walker, and Simon Woodward. "User-Friendly Methylation of Aryl and Vinyl Halides and Pseudohalides with DABAL-Me3." Advanced Synthesis & Catalysis 348, no. 6 (2006): 686–90. http://dx.doi.org/10.1002/adsc.200505405.

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6

Pinder, Joanne L., Rebecca E. Davis, and Jean-Damien Charrier. "A facile, one-pot procedure for the formation of benzimidazoles from esters using DABAL-Me3, an air stable source of AlMe3." Tetrahedron Letters 55, no. 35 (2014): 4853–55. http://dx.doi.org/10.1016/j.tetlet.2014.06.026.

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Pinder, Joanne L., Rebecca E. Davis, and Jean-Damien Charrier. "ChemInform Abstract: A Facile, One-Pot Procedure for the Formation of Benzimidazoles from Esters Using DABAL-Me3, an Air Stable Source of AlMe3." ChemInform 46, no. 6 (2015): no. http://dx.doi.org/10.1002/chin.201506161.

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8

Glynn, Daniel, David Bernier, and Simon Woodward. "ChemInform Abstract: Microwave Acceleration in DABAL-Me3-Mediated Amide Formation." ChemInform 40, no. 2 (2009). http://dx.doi.org/10.1002/chin.200902050.

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9

Cooper, Thea, Andrew Novak, Luke D. Humphreys, Matthew D. Walker, and Simon Woodward. "User-Friendly Methylation of Aryl and Vinyl Halides and Pseudohalides with DABAL-Me3." ChemInform 37, no. 33 (2006). http://dx.doi.org/10.1002/chin.200633067.

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Dissertations / Theses on the topic "DABAL-Me3"

1

FIORANI, GIULIA. "Synthesis and application of innovative solvents in carbon-carbon bond formation reactions." Doctoral thesis, Università degli Studi di Roma "Tor Vergata", 2010. http://hdl.handle.net/2108/1210.

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Abstract:
In questo lavoro sperimentale sono stati sintetizzati e caratterizzati diversi Liquidi Ionici. I Liquidi Ionici sintetizzati sono stati successivamente impiegati come solventi in reazioni di formazione di legame carbonio-carbonio. I Liquidi Ionici sono stati preparati e caratterizzati ottimizzando procedure riportate in letteratura. In alcuni casi i Liquidi Ionici sono stati preparati mediante reazioni che prevedevano riscaldamento con le microonde. La sintesi di Liquidi Ionici microonde assistita è stata perfezionata con l’aiuto di un programma di calcolo delle rese (CROW), a partire da dat
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