Efficient Synthesis of Various Substituted (Thio)Ureas, Semicarbazides, Thiosemicarbazides, Thiazolidones, and Oxadiazole Derived from [2.2]Paracyclophane.


Journal

ACS omega
ISSN: 2470-1343
Titre abrégé: ACS Omega
Pays: United States
ID NLM: 101691658

Informations de publication

Date de publication:
19 Apr 2022
Historique:
received: 07 01 2022
accepted: 23 02 2022
entrez: 27 4 2022
pubmed: 28 4 2022
medline: 28 4 2022
Statut: epublish

Résumé

The strategies of the syntheses of various (thio)ureas, semicarbazides, thiosemicarbazides, thiazolidones, and oxadiazole derived from the [2.2]paracyclophane molecule are achieved starting with 4-(2.2]paracyclophanyl)isocyanate. The structures of the obtained products were elucidated by NMR, mass spectrometry, and infrared (IR) spectroscopy in addition to high-resolution mass spectrometry (HRMS). X-ray structure analysis was also used to prove the assigned structure.

Identifiants

pubmed: 35474844
doi: 10.1021/acsomega.2c00141
pmc: PMC9026011
doi:

Types de publication

Journal Article

Langues

eng

Pagination

12879-12890

Informations de copyright

© 2022 The Authors. Published by American Chemical Society.

Déclaration de conflit d'intérêts

The authors declare no competing financial interest.

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Auteurs

Mohammed B Alshammari (MB)

Chemistry Department, College of Sciences and Humanities, Prince Sattam bin Abdulaziz University, P.O. 10, Box 83, Al-Kharij 11942, Saudi Arabia.

Ashraf A Aly (AA)

Chemistry Department, Faculty of Science, Minia University, 61519 El-Minia, Egypt.

Stefan Bräse (S)

Institute of Organic Chemistry, Karlsruhe Institute of Technology, 76131 Karlsruhe, Germany.
Institute of Biological and Chemical Systems (IBCS-FMS), Karlsruhe Institute of Technology, 76344 Eggenstein-Leopoldshafen, Germany.

Martin Nieger (M)

Department of Chemistry, University of Helsinki, P.O. Box 55 (A. I. Virtasen Aukio I), 00014 Helsinki, Finland.

Lamiaa E Abd El-Haleem (LE)

Chemistry Department, Faculty of Science, Minia University, 61519 El-Minia, Egypt.

Classifications MeSH