Results 21 to 30 of about 562 (194)

Synthetic Routes to Imidates and Their Applications in Organic Transformation: Recent Progress

European Journal of Organic Chemistry, Volume 26, Issue 39, October 16, 2023., 2023
Imidates are important organic intermediates used in several synthetic transformations towards N‐heterocycles, natural products and metal complexes with a potential catalytic effect. Herein, the recent synthetic approaches and diverse applications of imidates were categorized and summarized.
Andriani G. Chaidali, Ioannis N. Lykakis
wiley   +1 more source

Different Synthetic Methods for the Preparation of Triazolopyrimidines and their Biological Profile

ChemistrySelect, Volume 8, Issue 23, June 20, 2023., 2023
This review aims to give a broad overview of the synthetic methods, starting from aminotriazoles and pyrimidines, leading to heterocyclic systems containing the triazolopyrimidine ring and presenting the reactivity of these derivatives. Additionally, we have summarized the most important biological activities.
Achraf Hibot, Asmaa Oumessaoud, Abderrafia Hafid, Mostafa Khouili, Maria Dolors Pujol   +4 more
wiley   +1 more source

Reactions with Hydrazonoyl Halides. Part 21. Reinvestigation of the Reactions of Hydrazonoyl Bromides with 1,1-Dicyanothioacetanilide [PDF]

Journal of Chemical Research, 1999
The reaction of C-(benzoyl) -N- (phenyl) formohydrazonoyl bromide with 1,1-dicyanothioacetanilide was reinvestigated. The product was elucidated on the basis of elemental analysis, spectral data and alternative synthesis. Also, reaction of hydrazonoyl halides with different thioanilides were investigated.
Abdou O. Abdelhamid, Hussein F. Zohdi, Nora M. Rateb   +2 more
openaire   +1 more source

Recent developments in chemical reactivity of N,N-dimethylenamino ketones as synthons for various heterocycles [PDF]

, 2017
The current review presents recent progress in the utility of N,N-dimethyl enaminones as building blocks for a diverse range of acyclic, carbocyclic, five- and six-membered heterocyclic a broad range of heterocyclic and fused heterocyclic derivatives ...
Abbas, Abdallah, Abdallah, Abdallah, Abdel-Khalik, Abdel-Khalik, Abdel-Khalik, Abdel-Megid, Abdel-Motaleb, Abdel-Motaleb, Abdelhamid, Abdelhamid, AbdelKhalik, Abu-Shanab, Abu-Shanab, Adams, Agamy, Agamy, Al-Awadi, Al-Awadi, Al-Awadi, Al-Enezi, Al-Etaibi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Mousawi, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Omran, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Saleh, Al-Shiekh, Al-Shiekh, Al-Shiekh, Al-Zaydi, Al-Zaydi, Al-Zaydi, Al-Zaydi, Al-Zaydi, Al-Zaydi, Al-Zaydi, Alinezhad, Alinezhad, Almazroa, Anwer, Behbehani, Cao, Dawood, Domínguez, El-Desoky, El-Dusouqui, El-Taweel, Eldebss, Elghamry, Farghaly, Figueiredo, Gaber, Gaber, Gaber, Gaber, Gaber, Gaber, Gad-Elkareem, Gad-Elkareem, Ghozlan, Ghozlan, Ghozlan, Gomha, Gomha, Gomha, Gomha, Gomha, Greenhill, Hassanien, Hassanien, Hassanien, Hernández, Ho, Ho, Ho, Hughes, Ibrahim, Igarashi, Ingham, Jiang, Kandeel, Kantevari, Kascheres, Katritzky, Katritzky, Kenawi, Kepe, Kepe, Kim, Kirschbaum, Liu, Lue, Macba, Macba, Makhseed, Manley, Martins, Michael, Mokhtar, Mousawi, Moustafa, Mukhanova, Murphy, Negri, Nishimura, Nishiyama, Pichon, Pigge, Pleier, Raghunadh, Rasmussen, Reidlinger, Sabnis, Saleh, Salomone, Schenone, Shaaban, Shankaraiah, Sherif, Toche, Tois, Trautwein, Verma, Wan, Wan, Wan, Wan, Wan, Wang, Witherington, Xiang, Zhao, Zhou, Šimůnek   +153 more
core   +1 more source

Synthesis, Characterization and Molecular Docking of Novel Bioactive Thiazolyl-Thiazole Derivatives as Promising Cytotoxic Antitumor Drug

Molecules, 2015
Reactions of ethylidenethiocarbohydrazide with hydrazonoyl halides gave 1,3-thiazole or 1,3,4-thiadiazole derivatives according to the type of hydrazonoyl halides.
Sobhi M. Gomha, Taher A. Salaheldin, Huwaida M. E. Hassaneen, Hassan M. Abdel-Aziz, Mohammed A. Khedr   +4 more
doaj   +1 more source

Synthesis, in-silico studies, and biological evaluation of some novel 3-thiazolyl-indoles as CDK2–inhibitors

Results in Chemistry, 2023
The essential enzyme cyclin-dependent kinase 2 (CDK2) is a promising target for anticancer drug development due to its pivotal role in regulating the cell cycle. This study aimed to synthesize novel 3-thiazolyl-indole derivatives and assess their ability
Sobhi M. Gomha, Magdi E.A. Zaki, Deepika Maliwal, Raghuvir R.S. Pissurlenkar, Mohamed S. Ibrahim, Maher Fathalla, Ahmed M. Hussein   +6 more
doaj   +1 more source

Synthesis of Some New 1,3,4-Thiadiazole, Thiazole and Pyridine Derivatives Containing 1,2,3-Triazole Moiety

Molecules, 2017
In this study, 1-(5-Methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)ethan-1-one, was reacted with Thiosemicarbazide, alkyl carbodithioate and benzaldehyde to give thiosemicarbazone, alkylidenehydrazinecarbodithioate and 3-phenylprop-2-en-1-one-1,2,3-triazole ...
Nadia A. Abdelriheem, Ali M. M. Mohamed, Abdou O. Abdelhamid   +2 more
doaj   +1 more source

Hydrazonoyl Halides: Their Versatile Biological Activities

The Open Bioactive Compounds Journal, 2009
The various biological activities namely anthelmintic, antiarthropodal, antiviral, antimicrobial, herbicidal, antisarcoptic, acaricidal, insecticidal and miticidal activities exhibited by the hydrazonoyl halides are surveyed. Also, the uses of such halides as pesticides, weed controlling and antihypertensive agents as well as lipoxygenase and cyclo ...
Ahmad S.Shawali, Nevien A.Samy
openaire   +1 more source

A Novel Synthesis of 1,2,4-Triazolopteridines

Molecules, 2002
Reaction of 1,2-dihydro-2-thioxopteridin-4(3H)-one, 6,7-dimethyl-1,2-dihydro-2-thioxopteridin-4(3H)-one and 6,7-diphenyl-1,2-dihydro-2-thioxopteridin-4(3H)-one with hydrazonoyl halides affords the title compounds in good yields.
Hamdi M. Hassaneen, Manal A. Darwish, Tayseer A. Abdallah   +2 more
doaj   +1 more source

Synthesis and Biological Evaluation of Thiazolyl-Ethylidene Hydrazino-Thiazole Derivatives: A Novel Heterocyclic System

Applied Sciences, 2021
The reaction of 2-(1-(2-(2-(4-methoxybenzylidene)hydrazinyl)-4-methylthiazol-5-yl)ethylidene)hydrazinecarbothioamide with a range of hydrazonoyl chlorides and α-halo-compounds yielded three new series of thiazole derivatives.
Laila A. Al-Mutabagani, Fathy M. Abdelrazek, Sobhi M. Gomha, Ali S. Hebishy, Mohamed S. Abdelfattah, Safaa M. Hassan, Abdelwahed R. Sayed, Mahmoud M. Elaasser   +7 more
doaj   +1 more source