Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Z. F. Pavlova"'
Publikováno v:
Russian Journal of Organic Chemistry. 39:82-86
2-Arylthio- and 2-arylsulfonyl-1-nitro-1-phenylethenes react with amines to give the corresponding nitroenamines whose configuration (E or Z) depends on the amine structure. Primary amines gives rise to Z-nitroenamines, secondary cyclic amines with 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc7434ea3358624546946508a92c6cd2
https://doi.org/10.1023/a:1023494629499
https://doi.org/10.1023/a:1023494629499
Publikováno v:
Russian Journal of Organic Chemistry. 37:1259-1265
Reactions of 1-nitro-2-sulfonylalkenes with arenethiolates result in replacement of the sulfonyl group; the reactions with alkanethiolates are accompanied by subsequent addition of the reagent at the double bond to afford thioacetals. Less reactive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80031cea91e5913cdbd4569bf9aa2d91
https://doi.org/10.1023/a:1013119318658
https://doi.org/10.1023/a:1013119318658
Publikováno v:
Sulfur reports. 16:149-170
The synthesis and reactions of four groups of conjugated sulfur-containing compounds; i.e. 1-nitro-2(4)-thioethenes (and -dienes) and 1-nitro-2(4)-sulfonylethenes (and -dienes), which have become known in recent years, are discussed. Nitrothioethenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e8cab117a30240cae4d1e0cefba2790
https://doi.org/10.1080/01961779508048737
https://doi.org/10.1080/01961779508048737
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::471bc8391da38951eaf559d6b37a9b1f
https://doi.org/10.1002/chin.199118125
https://doi.org/10.1002/chin.199118125
Autor:
G. A. Berkova, Z. F. Pavlova, Ya. A. Kasem, E. S. Lipina, E. S. Mukhina, L. V. Mostyaeva, V. V. Perekalin
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dffc67d3bbfc7089e18851dd527dc376
https://doi.org/10.1002/chin.199152151
https://doi.org/10.1002/chin.199152151
Publikováno v:
ChemInform. 28
The synthesis and reactions of four groups of conjugated sulfur-containing compounds; i.e. 1-nitro-2(4)-thioethenes (and -dienes) and 1-nitro-2(4)-sulfonylethenes (and -dienes), which have become known in recent years, are discussed. Nitrothioethenes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3795fdab2604348902f9afd0471a39f
https://doi.org/10.1002/chin.199706281
https://doi.org/10.1002/chin.199706281
Publikováno v:
ChemInform. 33
Reactions of 1-nitro-2-sulfonylalkenes with arenethiolates result in replacement of the sulfonyl group; the reactions with alkanethiolates are accompanied by subsequent addition of the reagent at the double bond to afford thioacetals. Less reactive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40be22eaa4da1ba97f389fe1ce0839d8
https://doi.org/10.1002/chin.200221036
https://doi.org/10.1002/chin.200221036
Publikováno v:
ChemInform. 34
2-Arylthio- and 2-arylsulfonyl-1-nitro-1-phenylethenes react with amines to give the corresponding nitroenamines whose configuration (E or Z) depends on the amine structure. Primary amines gives rise to Z-nitroenamines, secondary cyclic amines with 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5a8c483764c3f3c0abaf4a922a89e11
https://doi.org/10.1002/chin.200328057
https://doi.org/10.1002/chin.200328057
Publikováno v:
ChemInform. 31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab4d0e3b6203fc205ce9073c2b4b9803
https://doi.org/10.1002/chin.200038034
https://doi.org/10.1002/chin.200038034
Publikováno v:
Chemischer Informationsdienst. 17
Conjugated 1,4-dinitrodienes react actively with arenethiols to form the products from substitution of the nitro group, i.e., nitroarylthiodienes. The characteristics of the IR and UV spectra of the obtained nitroarylthiodienes are explained by effec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7012cb9c93fff8ebda8e210e428e5dd4
https://doi.org/10.1002/chin.198611088
https://doi.org/10.1002/chin.198611088