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International Journal of Organic Chemistry (IJOC) is an international, specialized, English-language journal devoted to publication of original contributions concerning all field of organic chemistry. It is an open-access, peer-reviewed journal describing the synthetic approached and the design of new molecules for ap…
Shohei Sanada, Michinori Sumimoto, Kenji Hori
Acylation of allylic esters with acylsilanes and acylstannanes in the presence of a palladium complex was investigated theoretically using the DFT (B3PW91) method. We examined along the reaction that was reported by Tsuji’s. In this mechanism for generating a…
Sarkar M. A. Kawsar, Hamida A. Ara, Sheikh Aftab Uddin, Mohammed K. Hossain, Shagir A. Chowdhury, Abul F. M. Sanaullah, Mohammad A. Manchur, Imtiaj Hasan, Yukiko Ogawa, Yuki Fujii, Yasuhiro Koide, Yasuhiro Ozeki
A new N -acetylsulfanilylation series of uridine have been synthesized in good yield using direct acylation method and afforded the 5’- O-N -acetylsulfanilyluridine. In order to obtain newer products, the 5’- O-N -acetylsulfanilyluridine derivative was furthe…
William Kofie, Stephen Caddick, 1 1
The use of intramolecular reactions involving palladium/imidazolium salts to synthesize hetero-cyclic compounds is described. Reactivity of phenyl, ethyl and methyl substituents leading to isolation of various isomeric products is also illustrated. Rearrangem…
Hamdi M. Hassaneen, Zakaria Ahmed Gomaa
Refluxing of ( E )-5-amino-1-phenyl-3-styryl-1H-pyrazole-4-carbonitrile 2 with triethylor-thoformate in acetic anhydride afforded the corresponding formimidate 3. Treatment of 3 with hydrazine hydrate in ethanol afforded amino imino compound 4. Reaction of 4…
Mohammed Saleh Tawfik Makki, Reda Mohammdy Abdel-Rahman, Faisal Mohammed Aqlan
New fluorine substituted heterobicyclic nitrogen system as imidozolopyrimidines (2,3), pyrimido- 1,2,4-triazinones (4-7), 1,2,4-triazinyl-1,2,4-triazine (12-16), 1,2,4-triazinyl-1,2,4-triazinones (14-17) and substituted thiobarbituric acids (19-20), have been…
Samy B. Said, Mohammad M. A. Mashaly, Ahmed M. Sheta, Saad S. Elmorsy
An efficient and direct procedure for the synthesis of amidoalkylnaphthol derivatives employing a multi-component and one-pot condensation reaction of 2-naphthol, aromatic aldehyde and ace-tonitrile in the presence of tetrachlorosilane (TCS). A binary reagent…
Mahmoud Sayed Bashandy
This article describes the synthesis of some novel sulfonamides having the biologically active, thi-azole 4-6, 8, 10-12a,b, 20, 22, 34, 35, imidazo[1,2-a]pyridine 14, imidazo[2,1-c][1,2,4]triazole 15, imidazo[2,1-b]thiazole 23, 24, 33, nicotinonitrile 25, 1,3…
Mohammed Saleh Tawfek Makki, Reda Mohammady Abdel Rahman, Ola Ahmad Abu Ali
Some new fluorinated 3-N-acyl/3-N-alkylaminophenyl-1,2,4-triazino[3,4-b][1,3,4]thiadiazolones (2-12) have been obtained from treatment of 2-(4'-fluorophenyl)-6-(2'-amino-5'-fluorophenyl)-1,2,4-triazino[3,4-b][1,3,4]thiadiazol-4-one(1) with active functional o…
Hidetoshi Yamamoto, Masahiro Komeda, Ayana Ozaki, Michinori Sumimoto, Kenji Hori, Tsunemi Sugimoto
Beckmann rearrangements of oximes to lactams often require harsh conditions and/or the use of large amounts of acid catalyst. To reduce the amount of Bronsted acid required, and to avoid the formation of a large amount of undesirable byproducts under mild rea…
Marco A. Obregón-Mendoza, María Miriam Estévez-Carmona, Carolina Escobedo-Martínez, Manuel Soriano-García, Raúl G. Enríquez
Structures of 2-(naphthalen-2-ylmethyl)-2,3-dihydro-1H-indene-1,2-diol (C 20 H 18 O 2 ), compound 1 and 1-(3,4-dimethoxyphenyl)-3-methoxy-3-(4-nitrophenyl)propane-1,2-diol chloroform (C 18 H 21 NO 7 ·CHCl 3 ) compound 2 were established by spectral and X-ray…
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International Journal of Organic Chemistry (IJOC) is an international, specialized, English-language journal devoted to publication of original contributions concerning all field of organic chemistry. It is an open-access, peer-reviewed journal describing the synthetic approached and the design of new molecules for ap… All articles are open access under a CC BY 4.0 licence, with authors retaining copyright.
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