Results 201 to 210 of about 29,405 (265)

Reactivity of 2<i>H</i>-Azirines in Copper-Catalyzed Azide-Alkyne Cycloaddition Reactions. [PDF]

Org Lett
Janecký L, Madabeni A, Jelínková E, Klepetářová B, Rulíšek L, Beier P.   +5 more
europepmc   +1 more source

Single-crystal-to-single-crystal synthesis of a pseudostarch via topochemical azide-alkyne cycloaddition polymerization. [PDF]

Chem Sci, 2021
Ravi A, Shijad A, Sureshan KM.
europepmc   +1 more source

Coordination Studies of a Triazole‐Substituted 3H‐1,2,4‐Diazaphosphole: CC and CN Bond Activation Induced by Cobalt(0) and Nickel(0) Complexes

Zeitschrift für anorganische und allgemeine Chemie, EarlyView.
Reactions of a triazole‐substituted 3H‐1,2,4‐diazaphosphole with electron‐rich cobalt and nickel complexes result in the selective cleavage of CC and CN bonds on the triazole, forming chelate complexes with the activated diazaphosphole ligand. The reactivity of the recently reported 3H‐1,2,4‐diazaphosphole 1 toward electron‐rich Ni and Co complexes ...
Sebastian Hauer, Gábor Balázs, Justus Reitz, Max M. Hansmann, Robert Wolf   +4 more
wiley   +1 more source

Correction: Critical assessment of copper-alginate hydrogel beads as recyclable and heterogeneous catalysts for aqueous azide‒alkyne cycloaddition. [PDF]

Front Chem
Moglie Y, Buxaderas E, González Cabrera A, Díaz DD.   +3 more
europepmc   +1 more source

Making Blank Faces Expressive: Chemical Approaches to the Modification of Chemically Inert Peptides

Journal of Peptide Science, Volume 32, Issue 3, March 2026.
As an alternative to the conventional approach, which combines amino acid monomers in a one‐by‐one fashion to peptide derivatives, the chemical modification of existing peptides has attracted significant attention in recent years. However, such approaches generally target the reactive functional groups in cysteine and lysine residues, particularly in ...
Yoshitaka Moriyama, Hikari Sada, Takeshi Nanjo   +2 more
wiley   +1 more source

Copper-catalysed azide-alkyne cycloaddition on live M13 bacteriophage for expanding the molecular diversity of phage-displayed peptide libraries. [PDF]

RSC Chem Biol
Dawodu O, White CA, Specht C, Tapia A, Tharp JM.   +4 more
europepmc   +1 more source

Sulfated Ligands for the Copper(I)‐Catalyzed Azide–Alkyne Cycloaddition

, 2011
Wei Wang, Senglian Hong, Andrew Tran, Hao Jiang, Rebecca M. Triano, Yi Liu, Xing Chen, Peng Wu   +7 more
openalex   +2 more sources

Decreased PTGES2 Farnesylation in Granulosa Cells Compromises PGE2‐Dependent Cumulus Expansion and Oocyte Maturation During Ovarian Aging

Aging Cell, Volume 25, Issue 2, February 2026.
A schematic showing decreased PTGES2 farnesylation in granulosa cells compromises PGE2‐dependent cumulus expansion and oocyte maturation during ovarian aging. In young ovaries, PTGES2 farnesylation of GCs regulates the process of cumulus expansion and oocyte maturation by facilitating PGE2 production.
Sainan Zhang, Jiahui Qi, Chuanming Liu, Huidan Zhang, Bichun Guo, Die Wu, Yicen Liu, Xin Zhen, Yang Zhang, Nannan Kang, Jidong Zhou, Guijun Yan, Chaojun Li, Lijun Ding, Haixiang Sun   +14 more
wiley   +1 more source

Critical assessment of copper-alginate hydrogel beads as recyclable and heterogeneous catalysts for aqueous azide‒alkyne cycloaddition. [PDF]

Front Chem
Moglie Y, Buxaderas E, González Cabrera A, Díaz Díaz D.   +3 more
europepmc   +1 more source

Triply Responsive Control of Ion Transport with an Artificial Channel Creates a Switchable AND to OR Logic Gate

Angewandte Chemie, Volume 138, Issue 2, 9 January 2026.
We report a triply responsive artificial ion channel, showing tuneable activity, and responsive to three distinct stimuli ‐ light, pH, and ligand – which we use to formulate an AND to OR switchable molecular logic gate. Abstract Ion channels are ubiquitous in Nature, performing complex and essential tasks in our bodies. Synthetic chemists have begun to
Javid Ahmad Malla, Kharina J. Fenton, Adinarayana Bellamkonda, Samuel I. Fidler, Mark I. Wallace, Charlie T. McTernan   +5 more
wiley   +2 more sources