Eco-friendly and regiospecific intramolecular cyclization reactions of cyano and carbonyl groups in N,N-disubstituted cyanamide.

Moustafa, Amr H; Ahmed, Walaa W; Awad, Mohamed F; Aboelez, Moustafa O; Khodairy, Ahmed; Amer, Amer A

Moustafa, Amr H; Ahmed, Walaa W; Awad, Mohamed F; Aboelez, Moustafa O; Khodairy, Ahmed; Amer, Amer A.

Afiliación

Moustafa AH; Department of Chemistry, Faculty of Science, Sohag University, Sohag, 82524, Egypt. amr_hassanegypt@ymail.com.
Ahmed WW; Department of Chemistry, Faculty of Science, Sohag University, Sohag, 82524, Egypt.
Awad MF; Department of Biology, College of Science, Taif University, P.O. Box 11099, Taif, 21944, Saudi Arabia.
Aboelez MO; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Sohag University, Sohag, 82524, Egypt.
Khodairy A; Department of Chemistry, Faculty of Science, Sohag University, Sohag, 82524, Egypt.
Amer AA; Department of Chemistry, Faculty of Science, Sohag University, Sohag, 82524, Egypt.

Mol Divers ; 26(5): 2813-2823, 2022 Oct.

Article en En | MEDLINE | ID: mdl-35220547

Asunto(s)

Cianamida; Imidazoles; Aminas; Ciclización; Oxazoles; Propanoles; Solventes; Agua

Palabras clave

Eco-friendly reaction; Imidazole; Intramolecular cyclization; N-(4,6-Dimethylpyrimidin-2-yl)cyanamide; Oxazole; Regiospecificity

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cianamida / Imidazoles Idioma: En Revista: Mol Divers Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Egipto Pais de publicación: Países Bajos

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