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Departamento de Química Orgánica e Inorgánica, Facultad de Química, Universidad de Oviedo, Julián Clavería 8, E-33006 Oviedo, Spain
Author to whom correspondence should be addressed.
Academic Editor: Panayiotis A. Koutentis
Molbank 2021, 2021(2), M1198;
Received: 17 March 2021 / Revised: 24 March 2021 / Accepted: 25 March 2021 / Published: 26 March 2021
(This article belongs to the Section Organic Synthesis)
The title compound was synthesized by electrophilic cyanation of commercially available (R)-4-chloro-α-methylbenzylamine with cyanogen bromide in diethyl ether, and isolated as a yellow oil in 84% yield. It was characterized by 1H and 13C{1H] NMR, IR, HRMS, and specific rotation measurements. View Full-Text
Keywords: cyanamides; electrophilic cyanation; cyanogen bromide; amines; chiral molecules cyanamides; electrophilic cyanation; cyanogen bromide; amines; chiral molecules
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MDPI and ACS Style

González-Fernández, R.; Crochet, P.; Cadierno, V. N-[(1R)-1-(4-Chlorophenyl)ethyl]-Cyanamide. Molbank 2021, 2021, M1198.

AMA Style

González-Fernández R, Crochet P, Cadierno V. N-[(1R)-1-(4-Chlorophenyl)ethyl]-Cyanamide. Molbank. 2021; 2021(2):M1198.

Chicago/Turabian Style

González-Fernández, Rebeca; Crochet, Pascale; Cadierno, Victorio. 2021. "N-[(1R)-1-(4-Chlorophenyl)ethyl]-Cyanamide" Molbank 2021, no. 2: M1198.

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