Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Ahmed M. Abo-Bakr"'
Autor:
Dalal Nasser Binjawhar, Ola A. Abu Ali, Arwa Sultan Alqahtani, Eman Fayad, Ahmed M. Abo-Bakr, Antonous. M. Mekhael, Fayza M. Sadek
Publikováno v:
ACS Omega, Vol 9, Iss 16, Pp 18566-18575 (2024)
Externí odkaz:
https://doaj.org/article/438a54aef4a6402cb5c7dfaf2da4a9e8
Autor:
Heba E. Hashem, Ahmed M. Abo-Bakr
Publikováno v:
Heteroatom Chemistry, Vol 2019 (2019)
1,2,4-Triazine and 1,2,5-oxadiazine derivatives 2–12 were obtained from treated 1,3-oxazolone (1) with phenyl hydrazine or hydroxylamine hydrochloride. Chlorotriazine derivative 3 undergoing condensation reactions with different reagents produced n
Externí odkaz:
https://doaj.org/article/6d74cf072d594c85897cf51afd1ebdeb
Autor:
Mohamed Abd-Elsabour, Hytham F. Assaf, Ahmed M. Abo-Bakr, Abdulrahman G. Alhamzani, Mortaga M. Abou-Krisha, Aamal A. Al-Mutairi, Hesham M. Alsoghier
Publikováno v:
New Journal of Chemistry. 47:131-139
In this work, a green-electrochemical synthesis was applied to catechol oxidation (1) to o-benzoquinone (2) using cyclic voltammetry and potential controlled coulometry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a81f5613874b9f46d84cf5b68f17310
https://doi.org/10.1039/d2nj04530c
https://doi.org/10.1039/d2nj04530c
Publikováno v:
Fibers and Polymers. 23:2373-2383
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc57ceec0b90ac1981dd83a3d05fab71
https://doi.org/10.1007/s12221-022-4973-7
https://doi.org/10.1007/s12221-022-4973-7
Publikováno v:
Current Organic Synthesis. 19:558-568
Background: A series of new pyrimidines and thiazoles containing camphor moiety were synthesized under both conventional and microwave irradiation techniques. Methods: The condensation of camphor either with aminoguanidine or thiosemicarbazide gives
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a1de066ec838350058da505676e8047
https://doi.org/10.2174/1570179419666220104125340
https://doi.org/10.2174/1570179419666220104125340
Publikováno v:
Electroanalysis. 33:2476-2489
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab4a3df331be8a720c20bcf8089c69a6
https://doi.org/10.1002/elan.202100151
https://doi.org/10.1002/elan.202100151
Publikováno v:
Journal of the Iranian Chemical Society. 18:2757-2769
Camphor thiosemicarbazone 1 was utilized in the synthesis of new thiazolidinones. Thus, the reaction of 1 with ethyl bromoacetate, dimethyl acetylenedicarboxylate and maleic anhydride afforded the corresponding thiazolidinone 2, thiazolidinylidene ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::272425713b3a2a9512868249ae4998f1
https://doi.org/10.1007/s13738-021-02228-6
https://doi.org/10.1007/s13738-021-02228-6
Autor:
Ahmed M. Abo-Bakr, Heba E. Hashem
Publikováno v:
Heteroatom Chemistry, Vol 2019 (2019)
1,2,4-Triazine and 1,2,5-oxadiazine derivatives 2–12 were obtained from treated 1,3-oxazolone (1) with phenyl hydrazine or hydroxylamine hydrochloride. Chlorotriazine derivative 3 undergoing condensation reactions with different reagents produced n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de72a7c604d8791cabf4091fbcade3c6
https://doi.org/10.1155/2019/2326514
https://doi.org/10.1155/2019/2326514
Publikováno v:
RSC Advances. 9:13145-13152
In this paper, we present promising results in the green electrochemical oxidation of catechol in the presence of three different thiol nucleophiles at the surface of a glassy carbon electrode in an aqueous solution using cyclic voltammetry (CV). The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1933de69de0a190a5e139969a2ff064
https://doi.org/10.1039/c9ra01206k
https://doi.org/10.1039/c9ra01206k
Publikováno v:
Tetrahedron. 121:132913
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22282ae8f4423aff007d6595357a7cab
https://doi.org/10.1016/j.tet.2022.132913
https://doi.org/10.1016/j.tet.2022.132913