Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Manijeh Nematpour"'
Autor:
Nafiseh Karimi, Mohammad Mahboubi-Rabbani, Hossein Fasihi Dastjerdi, Manijeh Nematpour, Elham Rezaee, Sayyed Abbas Tabatabai
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 153:267-275
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f811d969244979708d067e17f8bf81d
https://doi.org/10.1007/s00706-022-02895-y
https://doi.org/10.1007/s00706-022-02895-y
Publikováno v:
Letters in Organic Chemistry. 19:34-40
A novel series of diimino dihydroquinazoline derivatives were synthesized from isocyanides and guanidine analogs in quantitative yields by applying an efficient, inexpensive, one-pot copper-catalyzed intramolecular C-H activation reaction under mild
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::131a23e210ca0900441462e426ebbee8
https://doi.org/10.2174/1570178618666210920112141
https://doi.org/10.2174/1570178618666210920112141
Publikováno v:
Letters in Organic Chemistry. 19:2-8
An unprecedented copper-catalyzed reaction of acetylene analogs with dialkyl azo dicarboxylate and benzazole analogs via a cross-coupling sequence was reported. A library of triazolobenzazole fused ring systems including [1,2,3] triazolo [3,4-b] [1,3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6034801aa4a58e964b135177c8607bbb
https://doi.org/10.2174/1570178618666211001120336
https://doi.org/10.2174/1570178618666211001120336
Autor:
Maryam Nili Ahmadabadi, Elham Rezaee, Manijeh Nematpour, Leila Karami, Shaya Mokhtari, Farzad Kobarfard, Sayyed Abbas Tabatabai
Publikováno v:
Iranian Journal of Pharmaceutical Research. 21
Background: Developing a potent and safe scaffold is challenging in anti-cancer drug discovery. Objectives: The study focused on developing novel series of compounds based on the inhibition of epidermal growth factor receptor tyrosine kinase (EGFR-TK
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::685a5acfe1fe477a3c511feabbee7843
https://doi.org/10.5812/ijpr-133840
https://doi.org/10.5812/ijpr-133840
Publikováno v:
Letters in Organic Chemistry. 17:832-836
A simple and appropriate procedure for the synthesis of quinazoline-2,4(1H,3H)-dione derivatives from isocyanides, aniline and isocyanate via the Cu-catalyzed intramolecular C-H activation reaction is reported. The advantages of this method are one-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cea85fde64e7fc1c1b7d31eea18ada9
https://doi.org/10.2174/1570178616666190905142545
https://doi.org/10.2174/1570178616666190905142545
Autor:
Maryam Bayanati, Sayyed Abbas Tabatabaia, Niloofar Parizadeh, Anna Sedaghat, Manijeh Nematpour
Publikováno v:
Journal of Sulfur Chemistry. 42:121-130
A novel class of substituted benzo[d]imidazo[5,1-b]thiazol-1-amine derivatives was synthesized utilizing a one-pot Cu-catalyzed cycloaddition of benzothiazole, trichloroacetonitrile, various amines and terminal alkynes in acetonitrile at room tempera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::804fd6901d2ad7236ea03e57b939848f
https://doi.org/10.1080/17415993.2020.1820010
https://doi.org/10.1080/17415993.2020.1820010
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 151:1591-1596
A novel class of substituted quinolines was synthesized through a one-pot, four-component sequential reaction by intramolecular C–H activation of isocyanides with N-sulfonylamidines, catalyzed by copper(I) iodide and l-proline as a ligand in aceton
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ca35878750863b92cea8d809a7e817a
https://doi.org/10.1007/s00706-020-02684-5
https://doi.org/10.1007/s00706-020-02684-5
Autor:
Elham Rezaee, Hossein Fasihi Dastjerdi, Manijeh Nematpour, Mehdi Jahani, Sayyed Abbas Tabatabai
Publikováno v:
Letters in Organic Chemistry. 17:704-708
A one-pot Cu-catalyzed synthesis of functionalized alkynyl imidamide by terminal alkynes, trichloroacetonitrile and aniline or benzyl amine is reported. The compounds were produced via coupling reaction of terminal alkynes with trichloroacetamidine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a2c00c3aa1de67d97d9b6557aeb72ec
https://doi.org/10.2174/1570178616666191023142821
https://doi.org/10.2174/1570178616666191023142821
Publikováno v:
Iranian journal of pharmaceutical research : IJPR. 21(1)
Impaired cell cycle regulation and disturbance in signal transduction pathway are two major causes of a condition defined as cancer, one of the significant reasons for mortality worldwide. Epidermal growth factor receptor tyrosine kinase inhibitors (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e367043891a1d4309131fe033279b980
https://pubmed.ncbi.nlm.nih.gov/35765503
https://pubmed.ncbi.nlm.nih.gov/35765503
Publikováno v:
Journal of Sulfur Chemistry. 41:146-153
An efficient synthesis of highly substituted thiophenes was developed by means of sulfonylketenimines in a multi-step reaction including heterocumulene system containing sulfur and nitro-alkanes with acidic α-hydrogen. The speed and ease of conducti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa5780ad17e444c58c216adfd3621dc9
https://doi.org/10.1080/17415993.2019.1699927
https://doi.org/10.1080/17415993.2019.1699927