Zobrazeno 1 - 10
of 74
pro vyhledávání: '"I. I. Kandror"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e20a8332240263cf27c6db4e7e1fc90
https://doi.org/10.1002/chin.199128272
https://doi.org/10.1002/chin.199128272
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f31d377c9fef2ec6cb8ae06a3db8a1d6
https://doi.org/10.1002/chin.199133228
https://doi.org/10.1002/chin.199133228
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::153cf33698228e807d581567d56a1d25
https://doi.org/10.1002/chin.199229112
https://doi.org/10.1002/chin.199229112
Autor:
M. A. Galkina, I. I. Kandror, B. D. Lavrukhin, I. O. Bragina, Yu. N. Belokon, Yu. G. Gololobov
Publikováno v:
ChemInform. 25
Ethyl α-cyanocarylate undergoes the Michael reaction with strong CH-acids (pKa < 13) in the presence of strong basic amines such as butylamine, piperidine, and triethylamine. Only polymerization of ethyl α-cyanoacrylate occurs under the same condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e48053f1715738610b2f496fd0869e83
https://doi.org/10.1002/chin.199426097
https://doi.org/10.1002/chin.199426097
Publikováno v:
ChemInform. 25
Functionally substituted thiols, i.e., thioglycolic acid and cysteamine and cysteine hydrochlorides, facilely undergo addition at the double bond of α-cyanoacrylates, forming the corresponding adducts in quantitative yields: R′SCH2CH(CN)COOR [R′
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ed7214e8194bc01d4b4f5dac749e62d
https://doi.org/10.1002/chin.199402134
https://doi.org/10.1002/chin.199402134
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 40:2456-2459
Functionally substituted thiols, i.e., thioglycolic acid and cysteamine and cysteine hydrochlorides, facilely undergo addition at the double bond of α-cyanoacrylates, forming the corresponding adducts in quantitative yields: R′SCH2CH(CN)COOR [R′
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::435203b557c24b44f59c65dee5d83c0d
https://doi.org/10.1007/bf00959721
https://doi.org/10.1007/bf00959721
Publikováno v:
Journal of Structural Chemistry. 32:269-272
An x-ray structural investigation of α-cyanoacrylic acid has been carried out (R=0.058 on the basis of 767 reflections). The molecules in the crystal are joined by strong O−H...N hydrogen bonds in zigzag chains along the [101] direction. The relat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86be8794deee399a8ae75b10fe9489b3
https://doi.org/10.1007/bf00777200
https://doi.org/10.1007/bf00777200
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 39:2538-2541
Various sulfhydryl compounds RSH (R=alkyl, aryl, acetyl, diethoxyphosphoryl and diethoxythiophosphoryl), unlike their oxygen analogs, easilyattack ethyl-α-cyanoacrylate forming adducts RSCH2CH(CN)COOC2H5 with high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a21a664039b7f7c29410f1471e17a20
https://doi.org/10.1007/bf01184534
https://doi.org/10.1007/bf01184534
Autor:
B. D. Lavrukhin, Yu. N. Belokon, I. I. Kandror, M. A. Galkina, Yu. G. Gololobov, I. O. Bragina
Publikováno v:
Bulletin of the Russian Academy of Sciences Division of Chemical Science. 41:1928-1930
Ethyl α-cyanocarylate undergoes the Michael reaction with strong CH-acids (pKa < 13) in the presence of strong basic amines such as butylamine, piperidine, and triethylamine. Only polymerization of ethyl α-cyanoacrylate occurs under the same condit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a37619cf5e67977d51193dd1e284c73e
https://doi.org/10.1007/bf00863836
https://doi.org/10.1007/bf00863836
Publikováno v:
Bulletin of the Russian Academy of Sciences Division of Chemical Science. 41:176-178
Syntheses are reported for representatives of a new class of derivatives of α-cyanoacrylic acid, namely, its salts with brucine, tert-butyldimethylamine, and diisopropylmethylamine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dfafe92a4910847a6159cf14977b0a9
https://doi.org/10.1007/bf00863941
https://doi.org/10.1007/bf00863941