Zobrazeno 1 - 10
of 13
pro vyhledávání: '"V. P. Nazaretian"'
Publikováno v:
Journal of Fluorine Chemistry. 84:135-139
New substituted cyano-and isocyanatodifluoromethanesulfonylfluorides were synthesized and their properties compared with halogenodifluoromethanesulfonylfluorides. NMR parameters are related to the electronegativity and covalent radii of substitutents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70196048e2c0ff36fadf268cf1c24408
https://doi.org/10.1016/s0022-1139(97)00055-9
https://doi.org/10.1016/s0022-1139(97)00055-9
Publikováno v:
Journal of Fluorine Chemistry. 69:237-240
Fluorination of cyclobutane- and cyclopentane-polycarboxylic acids having carboxylic groups in cis positions with SF4 yields mainly cyclization products, i.e. cyclic α,α,α',α'-tetrafluoroethers. 1,3-Cyclization was observed during fluorination of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b1ed29d9f4ced128b5b1109b79b9e87
https://doi.org/10.1016/0022-1139(93)02994-p
https://doi.org/10.1016/0022-1139(93)02994-p
Publikováno v:
Journal of Fluorine Chemistry. 69:225-229
Cyclopropanecarboxylic acids possessing more than one carboxylic group readily undergo fluorination when treated with SF 4 to yield the corresponding poly(trifluoromethyl)cyclopropanes and bicyclic ethers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2fff30a6f671a8715c64e97d75cf93e4
https://doi.org/10.1016/0022-1139(93)02996-r
https://doi.org/10.1016/0022-1139(93)02996-r
Publikováno v:
Journal of Fluorine Chemistry. 69:231-236
Treatment of gem -dichlorocyclopropanecarboxylic acids with SF 4 yields many rearranged products, i.e. 1,1-difluoro-substituted olefins. The mechanism of the rearrangement is discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4e118368fdf4a4e76331bfa88b249a4
https://doi.org/10.1016/0022-1139(93)02995-q
https://doi.org/10.1016/0022-1139(93)02995-q
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::433aa345e5390d482a678fc285b36672
https://doi.org/10.1002/chin.199520057
https://doi.org/10.1002/chin.199520057
Autor:
A. N. ALEXEENKO, V. P. NAZARETIAN
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fbc54b99d6e658c7572e21d42cda539
https://doi.org/10.1002/chin.199520058
https://doi.org/10.1002/chin.199520058
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51dfd9109b58c9c4c73f21accd484d7b
https://doi.org/10.1002/chin.199520056
https://doi.org/10.1002/chin.199520056
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97d46b173732752b015f14dcb96a3995
https://doi.org/10.1002/chin.199520055
https://doi.org/10.1002/chin.199520055
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17fc1830c71ac03924c2af39117a0271
https://doi.org/10.1002/chin.199806104
https://doi.org/10.1002/chin.199806104
Autor:
Yu. M. Pustovit, V. P. Nazaretian
Publikováno v:
Journal of Fluorine Chemistry. 55:29-36
New data on the fluorination of some carbonyl compounds with SF 4 contradict present views on the mechanism of this reaction. Results of the present and earlier studies have been used to discuss the accepted reaction mechanism and to suggest a modifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6b70083fd7463a4d987af596946a46c
https://doi.org/10.1016/s0022-1139(00)81250-6
https://doi.org/10.1016/s0022-1139(00)81250-6