共查询到20条相似文献,搜索用时 15 毫秒
1.
Olga V. Vinogradova 《Tetrahedron letters》2009,50(46):6358-6941
Cleavage of ortho-(dodeca-1,3-diynyl)triazenes in HCl or HBr medium and subsequent cyclization of the resulting diazonium salts is investigated. In the absence of a strong electron-withdrawing substituent, the reaction affords 3-alkynyl-4-bromo(chloro)cinnolines as the only product. A methoxycarbonyl group promotes hydrolysis of 4-halocinnolines which results in the formation of by-products: furo[3,2-c]cinnoline and cinnolinone. Substitution of bromine in 3-(alk-1-ynyl)-4-bromocinnolines is achieved with methylamine, Na2S and ethynylbenzene affording pyrrolo[3,2-c]cinnoline, thieno[3,2-c]cinnoline and 3,4-diethynylcinnoline, respectively. 相似文献
2.
O. V. Vinogradova V. N. Sorokoumov S. F. Vasilevskii I. A. Balova 《Russian Chemical Bulletin》2008,57(8):1725-1733
The Richter reaction of o-(alka-1,3-diynyl)arenediazonium salts, obtained by diazotization of diacetylenic derivatives of anilines, leads to 3-alkynyl-4-chloro-
or 3-alkynyl-4-bromocinnolines and/or 3-alkynyl-4-hydroxycinnolines (the latter cyclize into furo[3,2-c]-cinnolines under the reaction conditions). 3-Alkynyl-4-chlorocinnolines undergo solvolysis in methanol giving rise to 3-alkynyl-4-methoxycinnolines,
the subsequent hydrolysis of which also gives furo[3,2-c]cinnolines. Effects of the nature of substituents in the aromatic ring and of the reaction conditions on the product composition
and yields have been established. The reaction course has been studied by spectrophotometry.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1693–1700, August, 2008. 相似文献
3.
4.
5.
Data on the synthesis, reactions, crystal structure, and spectral characteristics of benzo[b]tellurophene, dibenzo[b,d]tellurophene, and their derivatives are reviewed and analyzed. 相似文献
6.
T. A. Stroganova A. V. Butin V. G. Kul'nevich 《Chemistry of Heterocyclic Compounds》2001,37(8):939-943
New derivatives of benzo[b]furan were obtained during successive bromination and dehydrobromination of alkanones containing a gem-difurylmethyl fragment. A mechanism is proposed for the transformations that occur. 相似文献
7.
8.
S. L. Bogza S. Yu. Suikov N. M. Bogdan Yu. A. Nikolyukin V. I. Dulenko 《Chemistry of Heterocyclic Compounds》2004,40(11):1421-1426
The recyclization reactions of 4-cyanobenzo[c]pyrylium salts with ammonia, primary amines, and hydrazines have been studied. New derivatives of isoquinoline, benzo-2,3-diazepine, and pyrazolo-[ 5,4-c]isoquinoline have been obtained.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1645–1651, November, 2004. 相似文献
9.
10.
11.
Two novel schemes have been developed for the synthesis of pyrrolocoumarin derivatives. A series of previously unknown 4,9-dimethylpyrano[3,2-e]indol-7(3H)-ones have been prepared.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No 10, pp. 1524–1532, October, 2004. 相似文献
12.
13.
S. V. Tolkunov A. I. Khyzhan S. Yu. Suikov V. I. Dulenko 《Chemistry of Heterocyclic Compounds》2005,41(3):379-386
Condensation of hetarene carboxaldehydes with phthalide gave 2-(3-hydroxy-1-oxoinden-2-yl)benzo[b]furan and 2-(3-hydroxy-1-oxoinden-2-yl)-5-ethylthieno[2,3-b]thiophene. Starting from hetaryl acetic acids gave 3-(3-hydroxy-1-oxoinden-2-yl)benzo[b]furan and 3-(3-hydroxy-1-oxoinden-2-yl)benzo[b]thiophene. Acylation of 3-hydroxy-1-oxoinden-2-yl-substituted heterocycles using acetic anhydride in the presence of 70% HClO4 leads to the formation of pentacyclic pyrilium salts. Pentacyclic indenopyridines are prepared by treating the pyrilium salts with ammonia. The reaction of the carbonyl group in the indenopyridines with hydroxylamine, hydrazine hydrate, and in reduction using NaBH4 has been studied.__________Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 435–443, March, 2005. 相似文献
14.
V. P. Rybalkin Ya. Yu. Vorobeva G. S. Borodkin A. D. Dubonosov A. V. Tsukanov V. V. Tkachev S. M. Aldoshin V. A. Bren V. I. Minkin 《Russian Chemical Bulletin》2005,54(12):2783-2789
New photochromic (2Z)-2-(N-acyl-N-arylaminomethylidene)benzo[b]thiophen-3(2H)-ones containing L-amino acid derivatives as migrating groups were synthesized. Light irradiation of their solutions at 436 nm leads to the
photoinduced acylotropic rearrangement N → O accompanied by migration of the chiral fragment. The bulky N-acyl group causes steric strain thus destabilizing the amide form of compounds and facilitating the photorearrangement.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2690–2696, December, 2005. 相似文献
15.
A. I. Markosyan R. A. Kuroyan S. V. Dilanyan M. S. Aleksanyan A. A. Karapetyan Yu. T. Struchkov 《Chemistry of Heterocyclic Compounds》2000,36(5):574-578
The reaction of 4-amino-3-ethoxycarbonyl-1,2-dihydrospiro(naphthalene-2,1-cyclopentane) with benzoyl isothiocyanate led to the corresponding 4-(N-benzoylthioureido) derivative, the cyclization of which gave 4-oxo-2-thioxo-1,2,3,4,5,6-hexahydrospiro(benzo[h]qquinazoline-5,1-cyclopentane). Condensation of the latter with hydrazine hydrate gave 2-hydrazino-3,4,5,6-tetrahydrospiro(benzo[h] quinazoline-5,1-cyclopentane), which formed 6-oxo-1H-7,8-dihydrospiro(benzo[h] triazolo[3,4-b] quinazoline7,1-cyclopentane) in reaction with orthoformice ester. Methylation of the product with methyl iodide led to its 2-methyl derivative.Communication 1, see ref. [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 658–662, May, 2000. 相似文献
16.
A. I. Markosyan R. A. Kuroyan S. V. Dilanyan 《Chemistry of Heterocyclic Compounds》2000,36(5):579-583
3-Substituted 4-oxo-2-thioxo-1,2,3,4,5,6-hexahydrospiro(benzo[h]quinazoline-5,1-cyclopentanes) were obtained by the reaction of 4-amino-3-ethoxycarbonyl-1,2-dihydrospiro(naphthalene-2,1-cyclopentane) with methyl, phenyl, and benzyl isothiocyanates and cyclization of the obtained thioureas. Condensation of the products with various halides gave 2,3-substituted 4-oxo-3,4,5,6-tetrahydrospiro(benzo[h]quinazoline-5,1-cyclopentanes). The reaction of 4-oxo-2-thioxo-1,2,3,4,5,6-hexahydrospiro(benzo[h]quinazoline-5,1-cyclopentane) with 1,2-dibromoethane and 1,3-dibromopropane led to 6-oxo-7,8-dihydrospiro(benzo[h]thiazolidino[2,3-b]quinazoline-7,1-cyclopentane) and 7-oxo-8,9-dihydrospiro(benzo[h]-perhydrothiazino[2,3-b]quinazoline-8,1-cyclopentane) respectively.A. L. Mndzhoyan Institute of Fine Organic Chemistry, National Academy of Sciences of the Republic of Armenia, Erevan. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 663–667, May, 2000. 相似文献
17.
A simple route to trans-2-hydroxymethyl-3-methylcyclopentanone was proposed. The compound is a key intermediate in the synthesis of natural spirocyclic sesquiterpene of the acorane series. 相似文献
18.
M. V. Vovk N. V. Mel'nichenko V. A. Chornous M. K. Bratenko 《Chemistry of Heterocyclic Compounds》2002,38(9):1096-1097
4-Isocyanato-3-(2-naphthyl)-1-phenylpyrazole cyclized under the influence of AlCl3 to give 2H-benzo[h]pyrazolo[4,3-c]isoquinoline. 相似文献
19.
M. V. Budnikova D. B. Rubinov P. V. Kurman A. L. Mikhal'chuk 《Chemistry of Heterocyclic Compounds》2003,39(1):101-109
Ionic hydrogenation of 8-aza-16-thiagona-1,3,5(10),13-tetraene-12,17-diones has been carried out by regioselective reduction of the carbonyl part of the aminovinylketothiolactone group to give 8-aza-16-thiagona-1,3,5(10),13-tetraen-17-ones. 相似文献