Academic literature on the topic 'N-acylcyanamides'

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Journal articles on the topic "N-acylcyanamides"

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Phakhodee, Wong, Dolnapa Yamano, and Mookda Pattarawarapan. "Ultrasound-Assisted Synthesis of N-Acylcyanamides and N-Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine." Synlett 31, no. 07 (January 28, 2020): 703–7. http://dx.doi.org/10.1055/s-0039-1691583.

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A convenient ultrasound-assisted one-pot synthesis of N-acylcyanamides starting from readily available carboxylic acids and sodium cyanamide has been developed. Upon activation in the presence of trichloroisocyanuric acid (TCCA) and triphenylphosphine, a range of carboxylic acids was converted into N-acylcyanamides in good to excellent yields within 10 minutes at room temperature without base. Remarkably, N-acyl-substituted imidazolones were readily accessible through guanylation-cyclization of the in situ generated N-acylcyanamides.
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Kwon, Chul Hoon, and Herbert T. Nagasawa. "Intermolecular decomposition of N-acylcyanamides." Journal of Organic Chemistry 55, no. 10 (May 1990): 3403–6. http://dx.doi.org/10.1021/jo00297a082.

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Courillon, C., M. Malacria, A. Servais, M. Azzouz, and D. Lopes. "Radical Cyclization of N-Acylcyanamides to Pyrroloquinazolines." Synfacts 2007, no. 4 (April 2007): 0364. http://dx.doi.org/10.1055/s-2007-968380.

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Looper, Ryan E., Travis J. Haussener, and James B. C. Mack. "Chlorotrimethylsilane Activation of Acylcyanamides for the Synthesis of Mono-N-acylguanidines." Journal of Organic Chemistry 76, no. 16 (August 19, 2011): 6967–71. http://dx.doi.org/10.1021/jo201264j.

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Looper, Ryan E., Travis J. Haussener, and James B. C. Mack. "ChemInform Abstract: Chlorotrimethylsilane Activation of Acylcyanamides for the Synthesis of Mono-N-acylguanidines." ChemInform 42, no. 50 (November 17, 2011): no. http://dx.doi.org/10.1002/chin.201150068.

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Larraufie, Marie-Hélène, Max Malacria, Christine Courillon, Cyril Ollivier, Louis Fensterbank, and Emmanuel Lacôte. "Synthesis of natural quinazolinones and some of their analogues through radical cascade reactions involving N-acylcyanamides." Tetrahedron 69, no. 36 (September 2013): 7699–705. http://dx.doi.org/10.1016/j.tet.2013.05.058.

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Atarod, Monireh, and Javad Safari. "Synergistic Effect between Ultrasound Irradiation and Na 2 CO 3 in N ‐Acylation Reaction: Applied for the Synthesis of Novel N ‐Acylcyanamide Derivatives." ChemistrySelect 5, no. 7 (February 17, 2020): 2219–24. http://dx.doi.org/10.1002/slct.201904793.

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Servais, Aurore, Meriam Azzouz, David Lopes, Christine Courillon, and Max Malacria. "Radical Cyclization of N-Acylcyanamides: Total Synthesis of Luotonin A." ChemInform 38, no. 20 (May 15, 2007). http://dx.doi.org/10.1002/chin.200720150.

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Dissertations / Theses on the topic "N-acylcyanamides"

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Beaume, Aurore. "Nouveaux accès à des polycycles azotés et carbonés par cascades radicalaires et réactions multi-composants." Paris 6, 2007. http://www.theses.fr/2007PA066285.

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Les cyclisations radicalaires en cascade de précurseurs insaturés conduisent à des polycycles complexes. La cyclisation radicalaire d’ynamides a été utilisée comme étape clé dans la synthèse totale de la mappicine, un alcaloïde polycyclique naturel. Les N-acylcyanamides, analogues azotés des ynamides, ont aussi été engagés dans des cascades radicalaires. La portée et le mécanisme de cette cascade ont été étudiés, notamment grâce à une modélisation faisant appel aux calculs DFT, et une chimiothèque a été synthétisée. La première synthèse totale par voie radicalaire sans étain de la luotonine A a été effectuée. D’autre part, le système palladium/norbornène a été utilisé dans l’élaboration d’une réaction multi-composants donnant accès à des dihydrophénanthrènes dissymétriques.
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Book chapters on the topic "N-acylcyanamides"

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Larraufie, Marie-Hélène. "Results: Developments of New Radical Cascades with N-Acylcyanamides." In Development of New Radical Cascades and Multi-Component Reactions, 39–78. Cham: Springer International Publishing, 2013. http://dx.doi.org/10.1007/978-3-319-01324-4_2.

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