Zobrazeno 1 - 10
of 10
pro vyhledávání: '"O. I. Osina"'
Publikováno v:
ChemInform. 32
The reaction of 2,3,5,6-tetrafluoropyridine-4-sulfonyl chloride with butadiene in a flow system at 510--520 °C afforded 1,3,4-trifluoroisoquinoline. A scheme of this process is proposed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69039857873697142aa2665a1cb3da7f
https://doi.org/10.1002/chin.200149109
https://doi.org/10.1002/chin.200149109
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac58b94e566d75ea403dd9e1adcbae83
https://doi.org/10.1002/chin.200147060
https://doi.org/10.1002/chin.200147060
Publikováno v:
Russian Chemical Bulletin. 50:322-323
The reaction of 2,3,5,6-tetrafluoropyridine-4-sulfonyl chloride with butadiene in a flow system at 510--520 °C afforded 1,3,4-trifluoroisoquinoline. A scheme of this process is proposed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6255135fb236428563aaac321ea856c6
https://doi.org/10.1023/a:1009559124641
https://doi.org/10.1023/a:1009559124641
Autor:
O. I. Osina, V. D. Shteingarts
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c611c6dbb3ee64ce36ee6e973e03f6be
https://doi.org/10.1002/chin.197421247
https://doi.org/10.1002/chin.197421247
Publikováno v:
Chemischer Informationsdienst. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::475cde3ad3cd07eb4992d79275d3222c
https://doi.org/10.1002/chin.198030162
https://doi.org/10.1002/chin.198030162
Autor:
V. D. Shteingarts, O. I. Osina
Publikováno v:
Chemischer Informationsdienst. 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a27505bc7d7e4af6e453b6e2ad18e139
https://doi.org/10.1002/chin.197421246
https://doi.org/10.1002/chin.197421246
Autor:
V. D. Shteingarts, O. I. Osina
Publikováno v:
Chemischer Informationsdienst. 14
Die Titelverbindung (1) wird mit den Nitrierungsreagenzien HNO3, HNO3/HF bzw. mit NO2BF4 umgesetzt.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ffc94ae8d01502666a42f7c05fd90f4
https://doi.org/10.1002/chin.198340119
https://doi.org/10.1002/chin.198340119
Publikováno v:
Chemischer Informationsdienst. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::929ca1d03193fcaa116c84cdb53f31d3
https://doi.org/10.1002/chin.198104192
https://doi.org/10.1002/chin.198104192
Publikováno v:
Chemischer Informationsdienst. Organische Chemie. 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc3ffcbfcbd950142804f9bf9f0284e5
https://doi.org/10.1002/chin.197031315
https://doi.org/10.1002/chin.197031315
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 35:2197-2197
The reaction of tertiary amines with alkyl halides give quarternary ammonium salts [i]. In contrast, heating 2-(pentafluorophenoxy)ethyl-N,N-diethylamine (I) with decyl bromide (II), 2-(pentafluorophenoxy)ethyl bromide (III) or 2-(pentafluorophenoxy)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef8934037f14ebde62bbef7733fd5994
https://doi.org/10.1007/bf00957571
https://doi.org/10.1007/bf00957571