Results 131 to 140 of about 298 (164)
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Journal of Heterocyclic Chemistry, 2016
New series of substituted thiazole and thiadiazoles were prepared starting from N′‐(3,4‐dihydronaphthalen‐1(2H)‐ylidene)hydrazinecarbothiohydrazide by reacting with different types of hydrazonoyl chlorides. In addition, 7‐(4‐chlorophenyl)‐5,6,6a,7‐tetrahydrobenzo [b]naphtha‐[1,2‐e][1,4]thiazepine reacted with hydrazonoyl halides to afford a new ...
Fatma A. A. El‐Hag +2 more
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New series of substituted thiazole and thiadiazoles were prepared starting from N′‐(3,4‐dihydronaphthalen‐1(2H)‐ylidene)hydrazinecarbothiohydrazide by reacting with different types of hydrazonoyl chlorides. In addition, 7‐(4‐chlorophenyl)‐5,6,6a,7‐tetrahydrobenzo [b]naphtha‐[1,2‐e][1,4]thiazepine reacted with hydrazonoyl halides to afford a new ...
Fatma A. A. El‐Hag +2 more
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A new efficient synthesis of pyrazoles from hydrazonoyl halides and β-oxophosphonates
Tetrahedron Letters, 2014Abstract A new practical and efficient synthesis of 1,3,5-trisubstituted pyrazoles has been developed by reacting of hydrazonoyl halides with β-oxophosphonates under mild conditions in good yields with excellent regioselectivity. This process employs an addition–elimination sequence. Wide scope, functional group compatibility has been established.
Aixue Sun +4 more
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ChemInform Abstract: REACTION OF HYDRAZONOYL HALIDES WITH N‐ARYL‐SUBSTITUTED BENZAMIDINES
Chemischer Informationsdienst, 1980AbstractHydrazonoylchloride (I) reagieren mit den N‐Arylbenzamidinen (II) zu Mischungen aus den Reaktionsprodukten (III)‐(VII).
F. ANZANI, P. DALLA CROCE, R. STRADI
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Hydrazonoyl Halides as Key Precursors for the Synthesis of Arylazo and Arylhydrazo Thiazoles
Mini-Reviews in Organic ChemistryAbstract: Hydrazonoyl halides are versatile precursors in organic synthesis and are widely employed for constructing heterocyclic frameworks, including arylazo and hydrazo thiazoles. These compounds exhibit significant biological activities, including antimicrobial, antitumor, antiinflammatory, and antioxidant properties, as well as have applications ...
Sobhi M. Gomha +5 more
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Tautomerism and Reactions of 1H-1,2,4-Triazole-5-thiones with Hydrazonoyl Halides
Journal f�r Praktische Chemie/Chemiker-Zeitung, 1998The acid dissociation constants (Ka) of a series of 3,4-diaryl-1H-1,2,4-triazole-5-thiones (1) were determined and were found to correlated linearly with Hammett substituent constants; log Ka = 1.06 σx − 11.01. Such a result indicates that 1 exists essentially in one tautomeric form namely the thione form.
Mosselhi A. N. Mosselhi +4 more
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Reactions with Hydrazonoyl Halides. Part 15.1 A Synthetic Approach to 2,3-Dihydrothiadiazoles
Journal of Chemical Research, 1998Hydrazonoyl halides 1 and 6a–f reacted with methyl hydrazinecarbodithioate (2) and methyl 3-[1-(aryl)alkylmethylidene]hydrazinecarbodithioates (9a–d or 10a,b), in ethanolic triethylamine solution, to afford the corresponding 2-hydrazono-3,5-diphenyl-2,3-dihydro-1,3,4-thiadiazoles (3), 5-methyl-2-methylsulfanyl-6-phenylhydrazono-1,3,4-thiadiazine (8 ...
Hussein A. Emam +2 more
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Reaction of hydrazonoyl halides with N‐aryl substituted benzamidines
Journal of Heterocyclic Chemistry, 1980AbstractThe reaction between hydrazonoyl halides and N‐arylbenzamidines leads to the simultaneous formation of products derived from a substitution and a cycloaddition reaction via two independent paths.
Fulvio Anzani +2 more
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ChemInform Abstract: Reactions of C‐(Dialkoxyphosphoryl)hydrazonoyl Halides with Acid Salts.
ChemInform, 1991AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
B. I. BUZYKIN, M. P. SOKOLOV
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Anti-Cancer Agents in Medicinal Chemistry, 2019
Background:The hydrazonoyl halides are presently an important target in the field of medicinal chemistry. The interest in the chemistry of hydrazonoyl halides is a consequence of the fact that they undergo a wide variety of reactions which provide routes to a myriad of both heterocyclic and acyclic compounds.
Magda F, Mohamed +11 more
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Background:The hydrazonoyl halides are presently an important target in the field of medicinal chemistry. The interest in the chemistry of hydrazonoyl halides is a consequence of the fact that they undergo a wide variety of reactions which provide routes to a myriad of both heterocyclic and acyclic compounds.
Magda F, Mohamed +11 more
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The Journal of Organic Chemistry
An efficient [3 + 2] cycloaddition reaction between in situ generated nitrile imines from hydrazonoyl halides and vinylsulfonium salts is developed. The nitrile imines are demonstrated to be a new class of reaction partner for vinylsulfonium salts to conduct the [3 + 2] cycloaddition reaction. The process provides a concise and efficient method for the
Wen-Jing Luo +7 more
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An efficient [3 + 2] cycloaddition reaction between in situ generated nitrile imines from hydrazonoyl halides and vinylsulfonium salts is developed. The nitrile imines are demonstrated to be a new class of reaction partner for vinylsulfonium salts to conduct the [3 + 2] cycloaddition reaction. The process provides a concise and efficient method for the
Wen-Jing Luo +7 more
openaire +2 more sources

