Zobrazeno 1 - 10
of 54
pro vyhledávání: '"E. K. Starostin"'
Autor:
M. A. Lapitskaya, Kasimir K. Pivnitsky, Gennady I. Nikishin, A. V. Ignatenko, E. K. Starostin
Publikováno v:
Russian Chemical Bulletin. 50:833-837
A convenient method for the synthesis of ω- and (ω – 1)-acetylenic acids involves free-radical oxidative scission of cycloalkanones containing five-, six, or seven-membered cycles to give the corresponding ω-olefinic acids followed by brominatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::732a67ae2ca39b0c6788a6d38b7d4db2
https://doi.org/10.1023/a:1011303024847
https://doi.org/10.1023/a:1011303024847
Publikováno v:
Mendeleev Communications. 19:334-336
Reactions of cycloalkanone enamines with H2O2 gave bis(1-morpholinocyclopent-1-yl)- and bis(1-morpholinocyclohex-1-yl)-peroxides, which were studied by NMR spectroscopy and X-ray diffraction. Thermolysis of bis(1-morpholinocyclohex-1-yl)-peroxide in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e6b4e17ed60b898f2ba1aad4104de6a
https://doi.org/10.1016/j.mencom.2009.11.014
https://doi.org/10.1016/j.mencom.2009.11.014
Publikováno v:
Mendeleev Communications. 18:123-125
The cocrystallization of di( cis -2-carboxycyclohexylcarbonyl) peroxide and cyclohexane-1,2-dicarboxylic acid from aqueous solution affords stable 1-carboxycyclohexyl radicals, which were identified by EPR spectroscopy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b0dbc2a075a7999aa060555524f3dd4
https://doi.org/10.1016/j.mencom.2008.05.003
https://doi.org/10.1016/j.mencom.2008.05.003
Publikováno v:
Russian Chemical Bulletin. 45:133-136
The decomposition of 2-chloro-, 2,2-dichloro-, and 2,6-dichloro-substituted cyclohexanone hydroperoxides on treatment with ferrous chloride and sulfate to give chloro-substituted aliphatic acids was investigated. A method for the synthesis of 2,6,6-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07a45a3be13c2b24894f484b939cd9ab
https://doi.org/10.1007/bf01433747
https://doi.org/10.1007/bf01433747
Autor:
Sergey Lindeman, E. K. Starostin, A. V. Ignatenko, Yu. T. Struchkov, Victor N. Khrustalev, Gennady I. Nikishin
Publikováno v:
Russian Chemical Bulletin. 44:907-912
The reaction ofmeso- andD,L-forms of bis(cyclohexyl)-2,2′-dione with a methanol solution of hydrogen peroxide in a neutral medium has been studied. It has been established that in the case of theD,L-formrac-(1R,4R,9S,10S)-1,4-dihydroxy-2,3-dioxatri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c9e5d77bde3e46a47b9aef9210fb72d
https://doi.org/10.1007/bf00696925
https://doi.org/10.1007/bf00696925
Autor:
L. N. Kalgorodova, G. I. Nikishin, Maxim G. Vinogradov, A. V. Ignatenko, E. K. Starostin, G. V. Chel'tsova-Bebutova, L. S. Gorshkova, E. A. Shapiro
Publikováno v:
Russian Chemical Bulletin. 44:167-171
A convenient preparative synthesis of cilastatin, an inhibitor of renal dipeptidase used in drugs with the antibiotic imipenem, has been elaborated. The key intermediate in this synthesis is 2-amino-7-chloroheptanoic acid prepared by oxidative cleava
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::757003c8c9d2970bc739c682a13a3db1
https://doi.org/10.1007/bf00696982
https://doi.org/10.1007/bf00696982
Publikováno v:
Russian Chemical Bulletin. 42:1174-1178
The decomposition of 1,4-dihydroxy-1,4-dihydroperoxycyclohexane under the action of FeSO4 and the decomposition of 1,4-cyclohexanedione monoethyleneketal hydroperoxide under the action of FeII salts in the presence of various ligands or under the act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7df5ac5a6dbdb5505c8d0dded44ab295
https://doi.org/10.1007/bf00702000
https://doi.org/10.1007/bf00702000
Publikováno v:
ChemInform. 24
A preparative method for the synthesis of α-haloadipic acids 4a-c by oxidative cleavage of 1,2-cyclohexanedione (1) in copper(II) halide/hydrogen peroxide or copper(II) halide (catalyst)/alkali metal halide/hydrogen peroxide system is reported
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40776b6a90e3cb685a30fb2b95bdc7d8
https://doi.org/10.1002/chin.199307164
https://doi.org/10.1002/chin.199307164
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df458cd7ea5126ebf27a1af98e7f2db2
https://doi.org/10.1002/chin.199431097
https://doi.org/10.1002/chin.199431097
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b3b3e19976dcd6a6156919878f23a38
https://doi.org/10.1002/chin.199504125
https://doi.org/10.1002/chin.199504125