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Preparation and characterization of the enol of acetamide: 1-aminoethenol, a high-energy prebiotic molecule. Artur Mardyukov, Felix Keul, Peter R. Schreiner , Chem. Sci. , 2020 , 11 , 12358

The enol of propionic acid. Akkad Danho, Artur Mardyukov, Peter R. Schreiner , Chem. Commun. , 2023

Matrix isolation and photorearrangement of cis- and trans-1,2-ethenediol to glycolaldehyde. Artur Mardyukov, Raffael C. Wende, Peter R. Schreiner , Chem. Commun. , 2023 , 59 , 2596

Mechanistical study on the formation of hydroxyacetone (CH3COCH2OH), methyl acetate (CH3COOCH3), and 3-hydroxypropanal (HCOCH2CH2OH) along with their enol tautomers (prop-1-ene-1,2-diol (CH3C(OH)CHOH), prop-2-ene-1,2-diol (CH2C(OH)CH2OH), 1-methoxyethen-1-ol (CH3OC(OH)CH2) and prop-1-ene-1,3-diol (HOCH2CHCHOH)) in interstellar ice analogs. Jia Wang, Joshua H. Marks, Andrew M. Turner, Anatoliy A. Nikolayev, Valeriy Azyazov, Alexander M. Mebel, Ralf I. Kaiser , Phys. Chem. Chem. Phys. , 2023 , 25 , 936

Chemical reactivity from the vibrational ground-state level. The role of the tunneling path in the tautomerization of urea and derivatives. Irea Mosquera-Lois, David Ferro-Costas, Antonio Fernández-Ramos , Phys. Chem. Chem. Phys. , 2020 , 22 , 24951

Synthesis of interstellar propen-2-ol (CH3C(OH)CH2) – the simplest enol tautomer of a ketone. Jia Wang, Anatoliy A. Nikolayev, Chaojiang Zhang, Joshua H. Marks, Valeriy N. Azyazov, André K. Eckhardt, Alexander M. Mebel, Ralf I. Kaiser , Phys. Chem. Chem. Phys. , 2023 , 25 , 17460

Co-ordination polymers of chelated heterocyclic dienols. M. Brierley, W. J. Geary , J. Chem. Soc. A , 1967 , 321

Infrared spectroscopic detection of ketene formation from carbene and CO sources: an amide synthesis. Packirisamy Kuzhalmozhi Madarasi, Chinnappan Sivasankar , New J. Chem. , 2020 , 44 , 8718

Chemoselective Staudinger-phosphite reaction of symmetrical glycosyl-phosphites with azido-peptides and polygycerols. Verena Böhrsch, Thresen Mathew, Maximilian Zieringer, M. Robert J. Vallée, Lukas M. Artner, Jens Dernedde, Rainer Haag, Christian P. R. Hackenberger , Org. Biomol. Chem. , 2012 , 10 , 6211

457. Quinoline series. Part III. Synthesis and reactions of quinoline-substituted ethylenes. H. Andrews, S. Skidmore, H. Suschitzky , J. Chem. Soc. , 1962 , 2370