1374746-88-9Relevant academic research and scientific papers
Alkyne-azide cycloaddition catalyzed by a dinuclear copper(I) complex
Chen, Hong-Bin,Abeyrathna, Nawodi,Liao, Yi
, p. 6575 - 6576 (2014)
A novel dinuclear copper complex CuI2(pip)2 was used as a catalyst for alkyne-azide cycloaddition (CuAAC) reaction. High yields (95-99%) were obtained for various substrates at a low loading of 0.2 mol %. The unique struct
Isopropanol and potassium tert-butoxide promoted intramolecular direct sp2 C-H functionalization: An expedient synthesis of 1,2,3-triazole annulated chromens and quinolones
Mondal, Biplab,Roy, Brindaban
supporting information, p. 6123 - 6127 (2015/10/28)
A series of 1,2,3-triazole annulated chromen and quinolone derivatives have been synthesized by means of direct sp2 C-H functionalization in the presence of iso-propanol and potassium tert-butoxide. The reaction proceeds through homolytic aroma
Glycerol: A biorenewable solvent for base-free Cu(i)-catalyzed 1,3-dipolar cycloaddition of azides with terminal and 1-iodoalkynes. Highly efficient transformations and catalyst recycling
Vidal, Cristian,Garcia-Alvarez, Joaquin
, p. 3515 - 3521 (2014/07/08)
The combination of CuI and glycerol exhibits a versatile and high catalytic activity in the Huisgen cycloaddition of azides and terminal or 1-iodoalkynes under standard bench experimental conditions (room temperature, under air and in the absence of a bas
Facile construction of [6,6]-, [6,7]-, [6,8]-, and [6,9]ring-fused triazole frameworks by copper-catalyzed, tandem, one-pot, click and intramolecular arylation reactions: Elaboration to fused pentacyclic derivatives
Nagarjuna Reddy,Kumara Swamy
experimental part, p. 2013 - 2022 (2012/05/05)
A sequential copper-catalyzed, one-pot, click reaction-intramolecular direct arylation, which involves two mechanistically distinct reactions (atom-economical click reaction and direct arylation of 1,2,3-triazole), to generate [6,6]-, [6,7]-, [6,8]-, and
