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72.
P. V. Pasternak V. I. Dyachenko Z. A. Starikova A. S. Peregudov M. Yu. Antipin N. D. Chkanikov 《Russian Chemical Bulletin》2006,55(7):1307-1308
Heating of 2-amino-1-aryl-1,4-dihydropyridines in acidic aqueous media gives 2-arylamino-1,4-dihydropyridines. The reaction
formally involves the migration of the aryl substituent from the endo-to exocyclic N atom.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1259–1260, July, 2006. 相似文献
73.
D. D. Nekrasov S. V. Kol'tsova M. A. Radishevskaya 《Chemistry of Heterocyclic Compounds》2004,40(3):301-307
The reaction of 5-aryl-2,3-dihydrofuran-2,3-diones with cyanoacetylhydrazide, o-(hydrazinocarbonyl)phenylthiourea, and the diphenylhydrazone of diaminoglyoxal leads to the synthesis of the corresponding N-cyanoacetylhydrazides of aroylpyruvic acids, 2-(N-aroylpyruvoylhydrazinocarbonyl)-phenylthioureas, and 5,6-bis(phenylhydrazono)-3-aroylmethylenepiperazin-2-ones. The results of the primary investigation of the biological activity of N-cyanoacetylhydrazides of aroylpyruvic acids are given. 相似文献
74.
I. B. Dzvinchuk 《Chemistry of Heterocyclic Compounds》2005,41(3):323-328
Cyanoethyl-, ethyl-, and methylhydrazones of 2-phenacyl-1H-benzimidazole undergo recyclization on condensation with aroyl chlorides or dimethylformamide with the formation of 5-(o-aroyl-aminoanilino)pyrazoles or 1-(5-pyrazolyl)-1H-benzimidazoles. The reaction with aroyl chlorides occurs selectively only with the corresponding cyanoethylhydrazone.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 372–378, March, 2005. 相似文献
75.
G. M. Abakarov M.-Z. V. Vagabov V. A. Pantin I. D. Sadekov V. I. Minkin 《Chemistry of Heterocyclic Compounds》2007,43(8):1076-1080
N-methyl-2-phenylbenzotellurazolinium iodide, like other N-methylbenzochalcogenazolium salts, readily undergoes reduction,
hydrolysis, and recyclization with hydrazine hydrate and o-phenylene diamine. 1-Methyl-2-phenylbenzotelluronioazole perchlorate
is an effective methylating agent in reactions with nucleophiles.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, 1268–1272, August, 2007. 相似文献
76.
77.
S. M. Ramsh A. V. Smirnova S. Yu. Solovyova Song Minyan 《Chemistry of Heterocyclic Compounds》2008,44(1):92-95
Mechanisms are given for reactions taking place upon heating 2-amino-5-benzylidene-1,3-thiazol-4(5H)-one in a medium consisting
of a secondary amine.
__________
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 111–114, January, 2008. 相似文献
78.
79.
The Use of Microwave Activation in the Chemistry of Heterocyclic Compounds. (Review) 总被引:1,自引:0,他引:1
N. N. Romanova P. V. Kudan A. G. Gravis Yu. G. Bundel' 《Chemistry of Heterocyclic Compounds》2000,36(10):1130-1140
Published data on the successful application of microwave activation in the chemistry of various heterocycles over the last two years are discussed. 相似文献
80.
Farid Naghiyev Ibrahim Mamedov Victor Khrustalev Namiq Shixaliyev Abel Maharramov 《中国化学会会志》2019,66(3):253-256
In this paper, we report a new synthesis route to 4H‐pyran derivatives and a plausible reaction mechanism. The interaction of 5‐acetyl‐2‐amino‐6‐methyl‐4‐phenyl‐4H‐pyran‐3‐carbonitrile with different active methylene reagents gives rise to the cleavage and subsequent recyclization of the pyran ring to afford the corresponding 4H‐pyran derivatives. 相似文献