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- Stimuli-responsive and self-healing supramolecular Zn(ii)–guanosine metal–organic gel for Schottky barrier diode application. Surbhi Singh, Atul Kumar Sharma, Hrushikesh M. Gade, Vidhi Agarwal, Rajendar Nasani, Nisha Verma, Bhagwati Sharma
, Soft Matter
, 2024
, 20
, 1025
- Subsecond detection of guanosine using fast-scan cyclic voltammetry. Michael T. Cryan, Ashley E. Ross
, Analyst
, 2019
, 144
, 249
- Functional architectures derived from guanine quartets. Jyotirmayee Dash, Puja Saha
, Org. Biomol. Chem.
, 2016
, 14
, 2157
- Synthesis of ribonucleotides from the corresponding ribonucleosides under plausible prebiotic conditions within self-assembled supramolecular structures. A. Franco, J. R. Ascenso, L. Ilharco, J. A. L. da Silva
, New J. Chem.
, 2020
, 44
, 2206
- Self-complementary hydrogen-bond interactions of guanosine: a hub for constructing supra-amphiphilic polymers with controlled molecular structure and aggregate morphology. Qian Xiao, Fei Song, Wu-Cheng Nie, Xiu-Li Wang, Yu-Zhong Wang
, Soft Matter
, 2019
, 15
, 102
- Identification of reaction sites and chlorinated products of purine bases and nucleosides during chlorination: a computational study. Fuhao Zhang, Yonghang Mo, Xiaomin Cao, Yingying Zhou, Yong Dong Liu, Rugang Zhong
, Org. Biomol. Chem.
, 2024
, 22
, 2851
- Development of a multi-enzyme cascade for 2′3′-cGAMP synthesis from nucleosides. Martin Becker, Isabel Nowak, Katharina Hildebrand, Stephan Lütz, Katrin Rosenthal
, Catal. Sci. Technol.
, 2024
- Toward potential supramolecular tissue engineering scaffolds based on guanosine derivatives. Lauren E. Buerkle, Horst A. von Recum, Stuart J. Rowan
, Chem. Sci.
, 2012
, 3
, 564
- Release of bioactive volatiles from supramolecular hydrogels: influence of reversible acylhydrazone formation on gel stability and volatile compound evaporation. Barbara Buchs (née Levrand), Wolfgang Fieber, Florence Vigouroux-Elie, Nampally Sreenivasachary, Jean-Marie Lehn, Andreas Herrmann
, Org. Biomol. Chem.
, 2011
, 9
, 2906
- Supramolecular gels made from nucleobase, nucleoside and nucleotide analogs. Gretchen Marie Peters, Jeffery T. Davis
, Chem. Soc. Rev.
, 2016
, 45
, 3188