Relevant bibliographies by topics / Propenamides

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Propenamides'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Propenamides"

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Andreev, Mikhail V., Vladimir A. Potapov, Maxim V. Musalov, and Lyudmila I. Larina. "First Examples of Reactions of 3-Trimethylsilyl-2-Propynamides and Organic Diselenides: Synthesis of Novel Derivatives of Propynamides." Catalysts 13, no. 10 (2023): 1326. http://dx.doi.org/10.3390/catal13101326.

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First examples of the reactions of 3-trimethylsilyl-2-propynamides with organic diselenides yielding 3-alkylselanyl-2-propenamides and 3-organylselanyl-2-propynamides were realized. The latter compounds were obtained by the Cu-catalyzed reaction of organic diselenides with 4-propioloylmorpholine. The reaction of 3-trimethylsilyl-2-propynamides with dialkyl diselenides in the system NaBH4/H2O/K2CO3/THF proceeded in a regio- and stereoselective fashion, affording 3-alkylselanyl-2-propenamides in 90–94% yields. An unsymmetrical divinyl selenide with the cyclic amide groups and a product, containi
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V. Andreev, Mikhail, Vladimir A. Potapov, Maxim V. Musalov, and Svetlana V. Amosova. "(Z,Z)-Selanediylbis(2-propenamides): Novel Class of Organoselenium Compounds with High Glutathione Peroxidase-Like Activity. Regio- and Stereoselective Reaction of Sodium Selenide with 3-Trimethylsilyl-2-propynamides." Molecules 25, no. 24 (2020): 5940. http://dx.doi.org/10.3390/molecules25245940.

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The efficient regio- and stereoselective synthesis of (Z,Z)-3,3′-selanediylbis(2-propenamides) in 76–93% yields was developed based on the reaction of sodium selenide with 3-trimethylsilyl-2-propynamides. (Z,Z)-3,3′-Selanediylbis(2-propenamides) are a novel class of organoselenium compounds. To date, not a single representative of 3,3′-selanediylbis(2-propenamides) has been described in the literature. Studying glutathione peroxidase-like properties by a model reaction showed that the activity of the obtained products significantly varies depending on the organic moieties in the amide group. D
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Martinez, Roberto, Luis Velasco, Lino Reyes T., Rocio Pozas H., Javier A. Carballo P., and Patricia Melchor M. "Electron impact mass spectrometry of N-(2-methylpropyl)-3-(o-,m- andp-R-phenyl)-2-propenamidesl." Spectroscopy 12, no. 1 (1994): 9–20. http://dx.doi.org/10.1155/1994/637030.

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Štetinová, Jarmila, Rudolf Kada, Ján Leško, Lubomír Zalibera, Dušan Ilavský, and Alexander Bartovič. "Synthesis and Properties of Substituted 1-(2-Benzothiazolyl)-2-pyridones." Collection of Czechoslovak Chemical Communications 60, no. 6 (1995): 999–1008. http://dx.doi.org/10.1135/cccc19950999.

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The studied 1-(2-benzothiazolyl)-2-pyridones Va-Vf were prepared from N-(2-benzothiazolyl)cyanoacetamide (II) which on reaction with 4-substituted benzaldehydes afforded 3-aryl-N-(2-benzothiazolyl)-2-cyano-2-propenamides IVa-IVg. Compounds IVa-IVf were cyclized with malonodinitrile in the presence of piperidine to give the corresponding pyridones Va-Vf.
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Štetinová, Jarmila, Rudolf Kada, Ján Leško, Miloslava Dandárová, and Marcela Krublová. "Synthesis and Spectral Properties of 1-(6-Methoxy-2-benzothiazolyl)-2-pyridones." Collection of Czechoslovak Chemical Communications 61, no. 6 (1996): 921–29. http://dx.doi.org/10.1135/cccc19960921.

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Substituted 1-(6-methoxy-2-benzothiazolyl)-2-pyridones 5a-5f have been prepared from N-(6-methoxy-2-benzothiazolyl)cyanoacetamide (2) which on reactions with 4-substituted benzaldehydes gives 3-aryl-2-cyano-N-(6-methoxy-2-benzothiazolyl)-2-propenamides 4a-4g. Derivatives 4a-4f were cyclized with malonodinitrile in the presence of piperidine to give the corresponding 2-pyridones 5a-5f. The IR, UV, 1H NMR and mass spectra of the substances synthesized are discussed.
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6

BouzBouz, Samir. "ChemInform Abstract: Synthesis and Reactivity of New Chiral 1-[(Trialkylsilyl)methyl]propenamides." ChemInform 42, no. 52 (2011): no. http://dx.doi.org/10.1002/chin.201152189.

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7

Kharas, Gregory B., Benjamin L. Hill, Monica V. Garcia, et al. "Novel Copolymers of Styrene. 8. Ring-Trisubstituted 2-Cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 52, no. 5 (2015): 331–35. http://dx.doi.org/10.1080/10601325.2015.1018802.

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Kharas, Gregory B., Najib J. Ayman, Rocelyn Calso, et al. "Novel Copolymers of Styrene. 11. Ring-Substituted 2-Cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 52, no. 6 (2015): 412–16. http://dx.doi.org/10.1080/10601325.2015.1029365.

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9

BouzBouz, Samir. "Studies in the Synthesis and Reactivity of New Chiral 1-[(Trialkylsilyl)-methyl]propenamides." Synlett 2011, no. 13 (2011): 1888–94. http://dx.doi.org/10.1055/s-0030-1260960.

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10

Kharas, Gregory B., Benjamin L. Hill, Vida M. Gaizutis, et al. "Novel Copolymers of Styrene. 3. Oxy Ring-disubstituted 2-cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 50, no. 6 (2013): 575–80. http://dx.doi.org/10.1080/10601325.2013.784166.

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Dissertations / Theses on the topic "Propenamides"

1

Ridge, Katerina. "The effects of structure and conformation on the reactivity of N-mono and N,N-disubstituted propenamides." Thesis, University of Surrey, 2015. http://epubs.surrey.ac.uk/807201/.

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This work describes the synthesis of twenty N-mono- and N,N-di-substituted propenamides and rationalises reactivity based on conformation. The N substituents are the 5,6,7,8-tetrahydro-1-naphthalenyl or 2,6-dimethylphenyl, and the benzoyl groups. The compounds also have substituents to the C=C group with a range of inductive and mesomeric effects. Synthesis was achieved mostly by acylation of amines/amides using acyl chlorides in the presence of a base. Fourteen novel compounds were synthesised (and six more, previously noted in the literature, were fully characterised for the first time); mel
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Book chapters on the topic "Propenamides"

1

Demaison, J. "305 C3H5NO 2-Propenamide." In Asymmetric Top Molecules. Part 2. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-10400-8_53.

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You might also be interested in the extended bibliographies on the topic 'Propenamides' for particular source types:
Journal articles
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