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pro vyhledávání: '"L. Chuiko"'
The article is devoted to the questions of raising productivity of a scoop inclined elevator. The actual direction is to develop more advanced bucket structures, which would lead to an increase in the productivity of the inclined bucket elevator by i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3eaf2e910559ffdac284a44d6ad908ff
Publikováno v:
Chemistry of Heterocyclic Compounds. 47:1137-1140
A method for the synthesis of [(thiazol-2-ylamino)methylene]bisphosphonic acids from (aminomethylene)-bisphosphonic acid through 3-N-unsubstituted (thioureidomethylene)bisphosphonic acid was proposed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f2e170f6e410458fa66450a0c1c898e
https://doi.org/10.1007/s10593-011-0884-z
https://doi.org/10.1007/s10593-011-0884-z
Akademický článek
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Autor:
L. Chuiko
Publikováno v:
Experiment. 15:51-54
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::399630cbcbfb4d3281cb69fb70ea3df2
https://doi.org/10.1163/2211730x-01501010
https://doi.org/10.1163/2211730x-01501010
Publikováno v:
Russian Journal of General Chemistry. 79:57-66
Substituted thioureidomethylenebisphosphonic acids react with haloketones to form thiazoles. The cyclization direction is predictably controlled by the size of the substituent. The NMR spectra of the resulting isomeric tetrazoles have well-defined di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::573abbe1eb0d6ef9781c4b08e4ab54c5
https://doi.org/10.1134/s1070363209010095
https://doi.org/10.1134/s1070363209010095
Publikováno v:
Russian Journal of General Chemistry. 79:67-71
The rate and pathway depends in a complicated manner of the cyclization reaction of phenylthioureidomethylenebisphosphonic acid with bromoacetone on the pH of the reaction medium. The dependence is explained in terms of formation of an intramolecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2887fc6c1a12857874bbd8960482cc38
https://doi.org/10.1134/s1070363209010101
https://doi.org/10.1134/s1070363209010101
Publikováno v:
Журнал органічної та фармацевтичної хімії; Том 13, № 2(50) (2015): Журнал органічної та фармацевтичної хімії; 57-63
Žurnal organìčnoï ta farmacevtičnoï hìmìï; Том 13, № 2(50) (2015): Žurnal organìčnoï ta farmacevtičnoï hìmìï; 57-63
Журнал органической и фармацевтической химии; Том 13, № 2(50) (2015): Журнал органической и фармацевтической химии; 57-63
Žurnal organìčnoï ta farmacevtičnoï hìmìï; Том 13, № 2(50) (2015): Žurnal organìčnoï ta farmacevtičnoï hìmìï; 57-63
Журнал органической и фармацевтической химии; Том 13, № 2(50) (2015): Журнал органической и фармацевтической химии; 57-63
Отримано ряд раніше невідомих похідних динітроанілінів, у структуру яких введені алкіламінні фрагенти та амінометилфосфонові групи у
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5218cb02ed08ee261d7b6932789dbb32
http://ophcj.nuph.edu.ua/article/view/ophcj.15.839
http://ophcj.nuph.edu.ua/article/view/ophcj.15.839
Publikováno v:
Journal of Plant Growth Regulation. 18:171-174
Derivatives of aminomethylenebisphosphonic acids constitute a class of promising herbicides. Replacement of the amino group by hydroxyl, ureido, thioureido, or imino moieties leads to compounds of significant herbicidal properties. This indicates tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba02eadf24f93caa594bfdb054cb4afd
https://doi.org/10.1007/pl00007066
https://doi.org/10.1007/pl00007066
Publikováno v:
ChemInform. 43
A method for the synthesis of N-3 unsubstituted (thioureidomethylene)bisphosphonic acid (IV) and the subsequent Hantzsch condensation to thiazoles (VI) are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6a72472afaa0c09363034cd3990faf4
https://doi.org/10.1002/chin.201221196
https://doi.org/10.1002/chin.201221196
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a873475939e5ba60ea304eedeb7f9744
https://doi.org/10.1002/chin.199407228
https://doi.org/10.1002/chin.199407228