Assessing the catalytic potential of novel halogen substituted carbene NHC (F, Cl, Br, I) catalysts in [3 + 2] cycloaddition reactions: A computational investigation

Ali A. Khairbek, Mohammad Abd-Al Hakim Badawi, Abdullah Y. Alzahrani and Renjith Thomas

Dalton Trans., 2024, 53, 16635
DOI: 10.1039/D4DT02225D

The chemistry of the s- and p-block elements with 2,2′:6′,2′′-terpyridine ligands

Andreas Winter, George R. Newkome and Ulrich S. Schubert

Inorg. Chem. Front., 2024, 11, 342
DOI: 10.1039/D3QI01245J

Development of First-in-Class Dual Sirt2/HDAC6 Inhibitors as Molecular Tools for Dual Inhibition of Tubulin Deacetylation

Laura Sinatra, Anja Vogelmann, Florian Friedrich, Margarita A. Tararina, Emilia Neuwirt, Arianna Colcerasa, Philipp König, Lara Toy, Talha Z. Yesiloglu, Sebastian Hilscher, Lena Gaitzsch, Niklas Papenkordt, Shiyang Zhai, Lin Zhang, Christophe Romier, Oliver Einsle, Wolfgang Sippl, Mike Schutkowski, Olaf Gross, Gerd Bendas, David W. Christianson, Finn K. Hansen, Manfred Jung and Matthias Schiedel

J. Med. Chem., 2023, 66, 14787
DOI: 10.1021/acs.jmedchem.3c01385

Click & sea: using bioorthogonal click chemistry to visualize seaweed cell walls

Wendy F Delpont, Godfrey Neutelings and Zoë A Popper

Annals of Botany, 2025, 136, 437
DOI: 10.1093/aob/mcaf103

Expedient Azide–Alkyne Huisgen Cycloaddition Catalyzed by a Combination of VOSO4 with Cu(0) in Aqueous Media

Wen-Chieh Yang and Chien-Tien Chen

ACS Org. Inorg. Au, 2024, 4, 235
DOI: 10.1021/acsorginorgau.3c00059

Click Reactions Meet Flow Chemistry: An Overview of the Applications of Click Chemistry under Continuous Flow Conditions

Nándor Kánya, Tamás Sándor Zsigmond, Tamás Hergert, Klára Lövei, György Dormán, Ferenc Kálmán and Ferenc Darvas

Org. Process Res. Dev., 2024, 28, 1288
DOI: 10.1021/acs.oprd.3c00364

Simultaneous ultrasound- and microwave-assisted one-pot ‘click’ synthesis of 3-formyl-indole clubbed 1,2,3-triazole derivatives and their biological evaluation

Jaydeep A. Mokariya, Anirudhdha G. Kalola, Pratibha Prasad and Manish P. Patel

Mol Divers, 2022, 26, 963
DOI: 10.1007/s11030-021-10212-8

Novel synthesis of 1,5-disubstituted-1,2,3-triazolines catalysed by Zepto magnetic microspheres under the influence of a rotating magnetic field

Priyanka Sharma, Srinivasu V. Vallabhapurapu, Wei H. Ho and Nanjundaswamy M. Hemmaragala

Can. J. Chem., 2019, 97, 163
DOI: 10.1139/cjc-2018-0349

Metallacrowns: an ideal platform for accessing lanthanide luminescence

Soroush Naseri and Vincent L. Pecoraro

Front. Chem. Biol., 2025, 4
DOI: 10.3389/fchbi.2025.1726839

A cascade reaction of cinnamyl azides with vinyl sulfones directly generates dihydro-pyrrolo-pyrazole heterocycles

Angela S. Carlson, Alexandru M. Petre and Joseph J. Topczewski

Tetrahedron Letters, 2021, 67, 152860
DOI: 10.1016/j.tetlet.2021.152860

Protein-Catalyzed Capture Agents

Heather D. Agnew, Matthew B. Coppock, Matthew N. Idso, Bert T. Lai, JingXin Liang, Amy M. McCarthy-Torrens, Carmen M. Warren and James R. Heath

Chem. Rev., 2019, 119, 9950
DOI: 10.1021/acs.chemrev.8b00660

Sequence-Defined Macrocycles for Understanding and Controlling the Build-up of Hierarchical Order in Self-Assembled 2D Arrays

James R. Dobscha, Henry D. Castillo, Yan Li, Rachel E. Fadler, Rose D. Taylor, Andrew A. Brown, Colleen Q. Trainor, Steven L. Tait and Amar H. Flood

J. Am. Chem. Soc., 2019, 141, 17588
DOI: 10.1021/jacs.9b06410

Easy Ligand Activation in the Coordination Sphere of Ru inside the [PW11O39]7– Backbone

Anna A. Mukhacheva, Artem L. Gushchin, Vadim V. Yanshole, Pavel A. Abramov and Maksim N. Sokolov

Molecules, 2020, 25, 1859
DOI: 10.3390/molecules25081859

Generation and Trapping of Nitrosocarbonyl Intermediates

Misal Giuseppe Memeo and Paolo Quadrelli

Chem. Rev., 2017, 117, 2108
DOI: 10.1021/acs.chemrev.6b00684

Fluorescent Ligands Enable Target Engagement Studies for the Intracellular Allosteric Binding Site of the Chemokine Receptor CXCR2

Max E. Huber, Silas Wurnig, Lara Toy, Corinna Weiler, Nicole Merten, Evi Kostenis, Finn K. Hansen and Matthias Schiedel

J. Med. Chem., 2023, 66, 9916
DOI: 10.1021/acs.jmedchem.3c00769

A decade of advances in the synthesis and biological potential of 1,2,3-triazolines

Yasmine Rahma Hachemi and Mohammed Hamadouche

Chem. Pap., 2025, 79, 8281
DOI: 10.1007/s11696-025-04379-9

Optimization of Covalent MKK7 Inhibitors via Crude Nanomole-Scale Libraries

Paul Gehrtz, Shir Marom, Mike Bührmann, Julia Hardick, Silke Kleinbölting, Amit Shraga, Christian Dubiella, Ronen Gabizon, Jan N. Wiese, Matthias P. Müller, Galit Cohen, Ilana Babaev, Khriesto Shurrush, Liat Avram, Efrat Resnick, Haim Barr, Daniel Rauh and Nir London

J. Med. Chem., 2022, 65, 10341
DOI: 10.1021/acs.jmedchem.1c02206

The chemistry and biology of mycolactones

Matthias Gehringer and Karl-Heinz Altmann

Beilstein J. Org. Chem., 2017, 13, 1596
DOI: 10.3762/bjoc.13.159

Synthesis and biological evaluation of 1, 2, 3-triazole incorporated pyrrole derivatives as anticancer agents

Somaiah Nalla, S. Aravind, Sri Charitha Annam, K. V. Padmavathi, Tasqeeruddin Syed and Mannam Subbarao

Synthetic Communications, 2024, 54, 1828
DOI: 10.1080/00397911.2024.2408605

Photocleavable Peptide–Poly(2-hydroxyethyl methacrylate) Hybrid Graft Copolymer via Postpolymerization Modification by Click Chemistry To Modulate the Cell Affinities of 2D and 3D Materials

Shin-nosuke Nishimura, Naoki Hokazono, Yukiko Taki, Hideki Motoda, Yusuke Morita, Koji Yamamoto, Nobuyuki Higashi and Tomoyuki Koga

ACS Appl. Mater. Interfaces, 2019, 11, 24577
DOI: 10.1021/acsami.9b06807

Metal-free and azide-free synthesis of 1,2,3-triazoles derivatives

Mukhtiar Ahmed, Hamaela Razaq, Muhammad Faisal, Ali N. Siyal and Azeem Haider

Synthetic Communications, 2017, 47, 1193
DOI: 10.1080/00397911.2017.1303511

Ultrasound-promoted organocatalytic enamine–azide [3 + 2] cycloaddition reactions for the synthesis of ((arylselanyl)phenyl-1H-1,2,3-triazol-4-yl)ketones

Gabriel P Costa, Natália Seus, Juliano A Roehrs, Raquel G Jacob, Ricardo F Schumacher, Thiago Barcellos, Rafael Luque and Diego Alves

Beilstein J. Org. Chem., 2017, 13, 694
DOI: 10.3762/bjoc.13.68

Copper(I)-Catalyzed Alkyne–Azide Cycloaddition (CuAAC) “Click” Reaction: A Powerful Tool for Functionalizing Polyhydroxylated Platforms

Héctor Manuel Pineda-Castañeda, Zuly Jenny Rivera-Monroy and Mauricio Maldonado

ACS Omega, 2023, 8, 3650
DOI: 10.1021/acsomega.2c06269

Biheterocyclic Coumarins: A Simple Yet Versatile Resource for Futuristic Design and Applications in Bio-molecular and Material Chemistry

Ashish Anand, Netravati Khanapurmath, Manohar V. Kulkarni and Tayur N. Guru Row

COC, 2022, 26, 444
DOI: 10.2174/1385272826666220301124149

Silver- and gold-catalyzed azide−alkyne cycloaddition by functionalized NHC-based polynuclear catalysts: Computational investigation and mechanistic insights

Ali A Khairbek, Mohammad Abd Al-Hakim Badawi, Abdullah Yahya Abdullah Alzahrani, Rajimon KJ and Renjith Thomas

Molecular Catalysis, 2025, 570, 114708
DOI: 10.1016/j.mcat.2024.114708

Versatile tissue‐injectable hydrogels capable of the extended hydrolytic release of bioactive protein therapeutics

Eric S. Nealy, Steven J. Reed, Steven M. Adelmund, Barry A. Badeau, Jared A. Shadish, Emily J. Girard, Kenneth Brasel, Fiona J. Pakiam, Andrew J. Mhyre, Jason P. Price, Surojit Sarkar, Vandana Kalia, Cole A. DeForest and James M. Olson

Bioengineering & Transla Med, 2024, 9
DOI: 10.1002/btm2.10668

Transition-state aromaticity and its relationship with reactivity in pericyclic reactions

Israel Fernández

Beilstein J. Org. Chem., 2025, 21, 1613
DOI: 10.3762/bjoc.21.125

(Phenylamino)pyrimidine-1,2,3-triazole derivatives as analogs of imatinib: searching for novel compounds against chronic myeloid leukemia

Luiz Claudio Ferreira Pimentel, Lucas Villas Boas Hoelz, Henayle Fernandes Canzian, Frederico Silva Castelo Branco, Andressa Paula de Oliveira, Vinicius Rangel Campos, Floriano Paes Silva Júnior, Rafael Ferreira Dantas, Jackson Antônio Lamounier Camargos Resende, Anna Claudia Cunha, Nubia Boechat and Mônica Macedo Bastos

Beilstein J. Org. Chem., 2021, 17, 2260
DOI: 10.3762/bjoc.17.144

1,3-Dipolar Cycloaddition of Nitrile Imines and Nitrile Oxides to Exocyclic C=N Bonds—An Approach to Spiro-N-Heterocycles

Juliana V. Petrova, Maxim E. Kukushkin and Elena K. Beloglazkina

IJMS, 2025, 26, 8673
DOI: 10.3390/ijms26178673

Synthesis of C-glycosyl-bis-1,2,3-triazole derivatives from 3,4,6-tri- $$\varvec{O}$$ O -acetyl-D-glucal

Anwar Shamim, Frederico B. Souza, Gustavo H. G. Trossini, Fernando M. Gatti and Hélio A. Stefani

Mol Divers, 2015, 19, 423
DOI: 10.1007/s11030-014-9564-0

Unravelling the regio- and stereoselective synthesis of bicyclic N,O-nucleoside analogues within the molecular electron density theory perspective

Nivedita Acharjee

Struct Chem, 2020, 31, 2147
DOI: 10.1007/s11224-020-01569-x