One-pot synthesis of new alkyl 1-naphthoates bearing quinoline, pyranone and cyclohexenone moieties


Journal

RSC advances
ISSN: 2046-2069
Titre abrégé: RSC Adv
Pays: England
ID NLM: 101581657

Informations de publication

Date de publication:
10 Nov 2021
Historique:
received: 22 09 2021
accepted: 09 11 2021
entrez: 2 5 2022
pubmed: 3 5 2022
medline: 3 5 2022
Statut: epublish

Résumé

A mild and one-pot synthetic pathway was successfully developed for the synthesis of new naphthoate-based scaffolds containing quinoline, pyranone and cyclohexenone moieties

Identifiants

pubmed: 35494386
doi: 10.1039/d1ra07092d
pii: d1ra07092d
pmc: PMC9043593
doi:

Types de publication

Journal Article

Langues

eng

Pagination

36748-36752

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

All authors declare that they have no conflict of interest associated with this publication.

Références

RSC Adv. 2020 Nov 26;10(70):42998-43009
pubmed: 35514936
ACS Infect Dis. 2020 Aug 14;6(8):2099-2109
pubmed: 32428392
Chem Commun (Camb). 2020 Jun 25;56(51):7025-7028
pubmed: 32452476
Bioorg Chem. 2021 Aug;113:105017
pubmed: 34091288
ACS Omega. 2020 Jul 19;5(29):18273-18288
pubmed: 32743203
Bioorg Chem. 2021 Sep;114:105076
pubmed: 34157555
Comput Biol Chem. 2020 Dec;89:107376
pubmed: 32979815
Chem Commun (Camb). 2015 Mar 25;51(24):5024-7
pubmed: 25703016
Curr Med Chem. 2002 Jun;9(12):1209-28
pubmed: 12052173
Mol Divers. 2022 Feb;26(1):309-329
pubmed: 33825097
Heliyon. 2020 Nov;6(11):e05558
pubmed: 33251371
Chemosphere. 2020 Apr;245:125602
pubmed: 31864042
Eur J Med Chem. 2019 Jan 1;161:252-276
pubmed: 30366253
Bioorg Chem. 2018 Feb;76:249-257
pubmed: 29197743
Phytochemistry. 2013 Apr;88:67-73
pubmed: 23351982
Spectrochim Acta A Mol Biomol Spectrosc. 2017 Mar 15;175:269-275
pubmed: 28064068
J Med Chem. 2007 Aug 23;50(17):3973-5
pubmed: 17658779
Front Chem. 2020 Dec 08;8:623971
pubmed: 33364229
ChemMedChem. 2020 Jun 4;15(11):907-932
pubmed: 32324951
RSC Adv. 2020 May 29;10(35):20552-20557
pubmed: 35517728
J Med Chem. 2022 Feb 24;65(4):2940-2955
pubmed: 34665619
J Med Chem. 2015 Dec 24;58(24):9639-52
pubmed: 26599611
Eur J Med Chem. 2021 Mar 5;213:113039
pubmed: 33261898

Auteurs

Seyedeh Hekmat Mousavi (SH)

Department of Chemistry, Faculty of Nano and Bioscience and Technology, Persian Gulf University Bushehr 75169 Islamic Republic of Iran f.mohammadsaleh@gmail.com +98 7731 223348.

Mohammad Reza Mohammadizadeh (MR)

Department of Chemistry, Faculty of Nano and Bioscience and Technology, Persian Gulf University Bushehr 75169 Islamic Republic of Iran f.mohammadsaleh@gmail.com +98 7731 223348.

Samira Poorsadeghi (S)

Department of Chemistry, Biology and Marine Science, Faculty of Science, University of the Ryukyus 1-Senbaru, Nakagami Nishihara Okinawa 903-0213 Japan.

Satoru Arimitsu (S)

Department of Chemistry, Biology and Marine Science, Faculty of Science, University of the Ryukyus 1-Senbaru, Nakagami Nishihara Okinawa 903-0213 Japan.

Fatemeh Mohammadsaleh (F)

Department of Chemistry, Faculty of Nano and Bioscience and Technology, Persian Gulf University Bushehr 75169 Islamic Republic of Iran f.mohammadsaleh@gmail.com +98 7731 223348.

Genta Kojya (G)

Center for Research Advancement and Collaboration, University of the Ryukyus Senbaru 1 Nishihara Okinawa 903-0213 Japan.

Shinichi Gima (S)

Center for Research Advancement and Collaboration, University of the Ryukyus Senbaru 1 Nishihara Okinawa 903-0213 Japan.

Classifications MeSH