Zobrazeno 1 - 10
of 122
pro vyhledávání: '"V. I. Staninets"'
Publikováno v:
Russian Journal of Organic Chemistry. 49:1168-1174
Anilides of 5-hexenoic acid react with arylsulfenyl chlorides in nitromethane in the presence of lithium perchlorate affording products of electrophilic cyclization, N-{6-[(arylsulfanyl)methyl]tetrahydro-2H-pyran-2-ylidene}anilinium perchlorates. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af753ed3890f90fd05432df5383af116
https://doi.org/10.1134/s1070428013080125
https://doi.org/10.1134/s1070428013080125
Publikováno v:
Russian Journal of Organic Chemistry. 49:123-129
Intramolecular electrophilic cyclization of 6-allylsulfanylpurine by the action of iodine and arenesulfenyl chlorides gave 7-iodomethyl-7,8-dihydro[1,3]thiazolo[2,3-i]purin-6-ium pentaiodide and 7-arylsulfanylmethyl-7,8-dihydro[1,3]thiazolo[2,3-i]pur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bcc916568057b94016a6df6c5d5a22c
https://doi.org/10.1134/s1070428013010211
https://doi.org/10.1134/s1070428013010211
Publikováno v:
Russian Journal of Organic Chemistry. 48:1536-1543
N-Aryl-4-phenylbut-3-enamides reacted with arenesulfenyl chlorides in chloroform to give N,4-diaryl-3-arylsulfanyl-4-chlorobutanamides, whereas in acetic acid in the presence of lithium perchlorate N-[4-arylsulfanyl-5-phenyltetrahydrofuran-2-ylidene]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02f515a01a56e37d8a60976b3f21afed
https://doi.org/10.1134/s107042801212007x
https://doi.org/10.1134/s107042801212007x
Autor:
V. I. Staninets, V. V. Orysyk, O.O. Obolentseva, V.M. Vovk, Volodymyr Bon, V.I. Pekhnyo, S.I. Orysyk, Yu. L. Zborovskii
Publikováno v:
Inorganica Chimica Acta. 382:127-138
Novel mono- and binuclear complexes of Zn(II) with thiourea derivatives (H2L) (N-2-propenyl-N′-2-pyridinylthiourea) and thiosemicarbazide, H3L (2-[(2-hydroxyphenyl)methylene]hydrazine-N-(2-propenyl)carbothioamide, (2-[(2-hydroxyphenyl)methylene]hyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c816cac9592cacb686a2dfea96030876
https://doi.org/10.1016/j.ica.2011.10.027
https://doi.org/10.1016/j.ica.2011.10.027
Publikováno v:
Russian Journal of Organic Chemistry. 48:193-201
N-Alkyl(aryl)amides of allylacetic acid when reacting with arylsulfenyl chlorides in acetic acid in the presence of lithium perchlorate undergo a selective cyclization to form N-{(2Z)-5-[(arylsulfanyl)methyl] dihydrofuran-2(3H)-ylidene}-N-alkyl-(aryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a05400905f75674ed4ae6f9bcba3cfb7
https://doi.org/10.1134/s1070428012020078
https://doi.org/10.1134/s1070428012020078
Publikováno v:
Chemistry of Heterocyclic Compounds. 47:1037-1042
The interaction of 3-allylsulfanyl-5H-[1,2,4]triazino[5,6-b]indole with iodine led to 1-iodomethyl-1,2-dihydro[1,3]thiazolo[2',3':3,4][1,2,4]triazino[5,6-b]indol-11-ium pentaiodide with an angular structure, on the basis of which 1-iodomethyl-1,2-dih
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4c3ad35f821b3b927dd37a7a5bc7212
https://doi.org/10.1007/s10593-011-0871-4
https://doi.org/10.1007/s10593-011-0871-4
Publikováno v:
Russian Journal of Organic Chemistry. 47:1066-1073
6-Allyl(diallyl, prop-2-yn-1-yl)amino-1-R-pyrazolo[3,4-d]pyrimidin-4(5H)-ones reacted with iodine to give angularly fused 8-iodomethyl-7,8-dihydro-1-R-imidazo[1,2-a]pyrazolo[4,3-e]pyrimidin-4(6H)-ones which were treated with sodium acetate to obtain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c48d12946a2db702a8ad873de6e7d193
https://doi.org/10.1134/s1070428011070165
https://doi.org/10.1134/s1070428011070165
Publikováno v:
Russian Journal of Organic Chemistry. 47:881-885
Cyclization of 2-(2-{4-[allylamino(thioxo)methyl]piperazin-1-yl}ethyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione by the action of iodine, bromine, or sulfuryl chloride gave 2-(2-{4-[4,5-dihydro-5-(halomethyl)-thiazol-2-yl]piperazin-1-yl}ethyl)-1H-benzo[
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af3c1680529229bb7733a9ab63135eff
https://doi.org/10.1134/s107042801106008x
https://doi.org/10.1134/s107042801106008x
Publikováno v:
Russian Journal of Organic Chemistry. 46:286-290
The reaction of 1-(4-oxo-1-R-5H-pyrazolo[3,4-d]pyrimidin-6-yl)-4-arylthiosemicarbazides with methyl iodide gave rise to 1,2,4-triazolo-pyrazolopyrimidinones of linear structure, and with dicyclohexylcarbodiimide the products had angular and linear st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::463cdf2446a3152cdea81586263bb737
https://doi.org/10.1134/s1070428010020235
https://doi.org/10.1134/s1070428010020235
Publikováno v:
Russian Journal of Organic Chemistry. 45:1847-1852
Reactions of 6-allylsulfanylpyrazolo[3,4-d]pyrimidin-4(5H)-one with arenesulfenyl chlorides in chloroform gave products of addition of the latter at the exocyclic double bond, while analogous reactions in acetic acid in the presence of LiClO4 were ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bf8d3a5ee332b0c162c0d14d40c0248
https://doi.org/10.1134/s1070428009120161
https://doi.org/10.1134/s1070428009120161