Zobrazeno 1 - 10
of 205
pro vyhledávání: '"Zohreh Mirjafary"'
Publikováno v:
Frontiers in Chemistry, Vol 12 (2024)
Deep eutectic solvent (DES) has been considered as a useful catalyst and reaction medium for various organic transformations. Herein, we report the catalytic application of novel deep eutectic solvent- based surfactant (DES surfactant) for the select
Externí odkaz:
https://doaj.org/article/185132bfcaa14fce98ed3c65910ef43c
Publikováno v:
Journal of Saudi Chemical Society, Vol 28, Iss 5, Pp 101915- (2024)
The development of novel and environmentally friendly solvents for chemical reactions is a vital in the pursuit of sustainable chemistry. This study presents a sustainable and efficient protocol for the rapid oxidation of benzaldehyde derivatives in
Externí odkaz:
https://doaj.org/article/3ea42f7652c242b3bd7d0f59f669d5a3
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract The aim of this research is to synthesize a new sulfonic acid catalyst based on halloysite nanotubes (Hal-Py-SO3H) and characterize it as a solid acid nanocatalyst by various analytical techniques such as Fourier-Transformed Infrared spectro
Externí odkaz:
https://doaj.org/article/c1561fc6e22c44159829327d0ba0291e
Autor:
Parsa Hesamzadeh, Abdolvahab Seif, Kazem Mahmoudzadeh, Mokhtar Ganjali Koli, Amrollah Mostafazadeh, Kosar Nayeri, Zohreh Mirjafary, Hamid Saeidian
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-18 (2024)
Abstract Antioxidant peptides (AOPs) are highly valued in food and pharmaceutical industries due to their significant role in human function. This study introduces a novel approach to identifying robust AOPs using a deep generative model based on seq
Externí odkaz:
https://doaj.org/article/546bdcb34f0743a2ae2c1ee1f0c7c2ec
Publikováno v:
Journal of Ionic Liquids, Vol 4, Iss 2, Pp 100111- (2024)
Acidic ionic liquids are a subset of ionic liquids where the cation or anion possess acidic properties with huge applications in various fields. Here we describe environmentally safe and highly efficient conjugate addition of aromatic and aliphatic a
Externí odkaz:
https://doaj.org/article/a8c35eb8551c4dbbbd818a1bedaa6967
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Ionogels are gaining popularity as a potential replacement for volatile organic solvents in various processes, such as catalysts, electrochemistry, spectroscopy, and medicinal chemistry, due to their low toxicity, high thermal stability, and
Externí odkaz:
https://doaj.org/article/817618c3f20e433785f1b1a24e1b772e
Autor:
Zohreh Mirjafary, Mahdieh Mohammad Karbasi, Parsa Hesamzadeh, Hamid Reza Shaker, Asghar Amiri, Hamid Saeidian
Publikováno v:
Molecules, Vol 27, Iss 23, p 8555 (2022)
A new series of 1,2,3-triazole derivatives 5a–f based on benzothiazole were synthesized by the 1,3-dipolar cycloaddition reaction of S-propargyl mercaptobenzothiazole and α-halo ester/amide in moderate to good yields (47–75%). The structure of a
Externí odkaz:
https://doaj.org/article/e988b612dc064ebda46caa161ae98c19
Autor:
Rasoul Shahbazi, Davoud Jafari-Gharabaghlou, Zohreh Mirjafary, Hamid Saeidian, Nosratollah Zarghami
Publikováno v:
Pharmacological Reports. 75:442-455
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::effa5a1d54a09072e09af94493056dbf
https://doi.org/10.1007/s43440-023-00462-8
https://doi.org/10.1007/s43440-023-00462-8
Publikováno v:
New Journal of Chemistry. 47:5863-5874
The cyclopentadiene (Cp) hyperconjugative aromaticity on anomeric carbon of piperidines was studied using DFT method. The aromaticity indices showed that Cp has considerably enhanced cyclic conjugation in comparison with unsubstituted Cp.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adeeb5907b43d580125d25d809f4e36e
https://doi.org/10.1039/d3nj00337j
https://doi.org/10.1039/d3nj00337j
Publikováno v:
Research on Chemical Intermediates. 48:3685-3699
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9e56906c04097a5075ce75c6fe24404
https://doi.org/10.1007/s11164-022-04781-y
https://doi.org/10.1007/s11164-022-04781-y