Computational studies on CuAAC reaction mechanism with [CuX(PPh3)]; X = I, Br, Cl for the synthesis of 4- and 5-halo-1,2,3-triazoles

[1] Kolb HC(2001)Click chemistry: diverse chemical function from a few good reactions Angew Chem Int Ed 40 2004-2021

[2] Finn MG(2021)Remote ether groups-directed regioselective and chemoselective cycloaddition of azides and alkynes Chin Chem Lett 32 4019-4023

[3] Sharpless KB(2023)A brief survey on the application of metal-catalyzed azide–alkyne cycloaddition reactions to the synthesis of ferrocenyl-x-1, 2, 3-triazolyl-R (x = none or a linker and R= organic entity) compounds with anticancer activity Coord Chem Rev 479 214996-628

[4] Duan X(2023)The fate of heterogeneous catalysis & click chemistry for 1, 2, 3-triazoles: nobel prize in chemistry 2022 Catal Commun 176 106629-2711

[5] Zheng N(2021)Metals as “click” catalysts for alkyne-azide cycloaddition reactions: an overview J Organomet Chem 944 121846-3064

[6] Li M(1989)Kinetics and reaction mechanisms: selected examples from the experience of forty years Pure Appl Chem 61 613-3015

[7] Sun X(2002)A stepwise huisgen cycloaddition process: copper (I)-catalyzed regioselective “ligation” of azides and terminal alkynes Angew Chem 114 2708-1315

[8] Lin Z(2002)Peptidotriazoles on solid phase:[1, 2, 3]-triazoles by regiospecific copper (I)-catalyzed 1, 3-dipolar cycloadditions of terminal alkynes to azides J Org Chem 67 3057-4701

[9] Qiu P(2008)Cu-catalyzed azide− alkyne cycloaddition Chem Rev 108 2952-10012

[10] Song W(2010)Copper-catalyzed azide–alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper (I) acetylides Chem Soc Rev 39 1302-6511

[1] Kolb HC(2001)Click chemistry: diverse chemical function from a few good reactions Angew Chem Int Ed 40 2004-2021

[2] Finn MG(2021)Remote ether groups-directed regioselective and chemoselective cycloaddition of azides and alkynes Chin Chem Lett 32 4019-4023

[3] Sharpless KB(2023)A brief survey on the application of metal-catalyzed azide–alkyne cycloaddition reactions to the synthesis of ferrocenyl-x-1, 2, 3-triazolyl-R (x = none or a linker and R= organic entity) compounds with anticancer activity Coord Chem Rev 479 214996-628

[4] Duan X(2023)The fate of heterogeneous catalysis & click chemistry for 1, 2, 3-triazoles: nobel prize in chemistry 2022 Catal Commun 176 106629-2711

[5] Zheng N(2021)Metals as “click” catalysts for alkyne-azide cycloaddition reactions: an overview J Organomet Chem 944 121846-3064

[6] Li M(1989)Kinetics and reaction mechanisms: selected examples from the experience of forty years Pure Appl Chem 61 613-3015

[7] Sun X(2002)A stepwise huisgen cycloaddition process: copper (I)-catalyzed regioselective “ligation” of azides and terminal alkynes Angew Chem 114 2708-1315

[8] Lin Z(2002)Peptidotriazoles on solid phase:[1, 2, 3]-triazoles by regiospecific copper (I)-catalyzed 1, 3-dipolar cycloadditions of terminal alkynes to azides J Org Chem 67 3057-4701

[9] Qiu P(2008)Cu-catalyzed azide− alkyne cycloaddition Chem Rev 108 2952-10012

[10] Song W(2010)Copper-catalyzed azide–alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper (I) acetylides Chem Soc Rev 39 1302-6511