951775-12-5Relevant academic research and scientific papers
Copper(II)-dipicolinate-mediated clickable azide–alkyne cycloaddition in water as solvent
Bahsis, Lahoucine,Ben El Ayouchia, Hicham,Anane, Hafid,Triki, Smail,Julve, Miguel,Stiriba, Salah-Eddine
, p. 633 - 643 (2018)
Copper(II)-dipicolinate complex [CuII(dipic)(H2O)2] (1) (H2L?=?dipicolinic acid (H2dipic)) was synthesized via oxidation of copper(I) iodide and pyridine-2,6-dicarboxylic acid in water and acetonitril
An enolate-mediated regioselective synthesis of 1,2,3-triazoles via azide-aldehydes or ketones [3+2]-cycloaddition reactions in aqueous phase
Chavan, Subhash P.,Joshi, Sameer M.,Llop, Jordi,Rode, Chandrashekhar V.,Tripathi, Anupam
supporting information, (2020/02/13)
A synthetic route for the direct conversion of arylazides into the corresponding trizoles via phase transfer catalyst-assisted [3+2] cycloaddition reaction under basic conditions in aqueous medium is reported. This synthetic methodology, which offers high
A supercritical carbon dioxide in the synthesis of 1, 2, 3 - triazole class is the compound of the method
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Paragraph 0054; 0055; 0056, (2018/04/03)
The invention discloses a method for synthesizing a 1,2,3-triazole compound in supercritical carbon dioxide and belongs to the technical field of synthesis of 1,2,3-triazole compounds. The key point of the technical scheme of the invention is as follows:
A facile one-pot metal-free synthesis of 1,4-disubstituted 1,2,3-triazoles
Jia, Qianfa,Yang, Gongming,Chen, Lei,Du, Zhiyun,Wei, Jia,Zhong, Yanqiong,Wang, Jian
supporting information, p. 3435 - 3440 (2015/06/08)
Abstract A 1,3-dipolar cycloaddition reaction of commercially available aldehydes with azides and secondary amines through a one-pot strategy has been developed. This method furnishes 1,4-disubstituted 1,2,3-triazoles in good to excellent yields and high
An organocatalytic azide-aldehyde [3+2] cycloaddition: High-yielding regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles
Ramachary, Dhevalapally B.,Shashank, Adluri B.,Karthik
supporting information, p. 10420 - 10424 (2016/02/18)
An organocatalytic azide-aldehyde [3+2] cycloaddition (organo-click) reaction of a variety of enolizable aldehydes is reported. The organo-click reaction is characterized by a high rate and regioselectivity, mild reaction conditions, easily available subs
Microwave-assisted azide-alkyne cycloaddition in water using a heterogeneous Cu-catalyst
Jacob, Katharina,Stolle, Achim
, p. 1251 - 1257 (2014/04/17)
Several triazoles have been synthesized. They were obtained by a Cu-catalyzed cycloaddition of azides and alkynes. The reaction takes place in aqueous media under microwave irradiation using a copper catalyst based on porous glass. The products have been
