Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Methyl thiocyanate"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Russian Journal of Organic Chemistry. 57:186-194
1-Mono- and 1,4-difunctional diamantane derivatives were synthesized by the reaction of diamantane with nitric acid or a HNO3–AcOH mixture followed by the addition of nitrogen-containing nucleophiles. Methyl N-(diamantan-1-yl)carbamothioate was syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de782fc68797a989fbc31c4894375a88
https://doi.org/10.1134/s1070428021020081
https://doi.org/10.1134/s1070428021020081
Autor:
Anastasiya Yu. Kharintseva, Kseniya А. Stepanova, Dmitry N. Babentsev, Anastasiya E. Simakhina, Maksim V. Dmitriev, Vladimir А. Glushkov
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:63-68
4-Aryl-2-methylbutan-2-ols with methoxy or methylenedioxy substituents participate in the Graf–Ritter reaction with methyl thiocyanate in the presence of an acid (H2SO4, MeSO3H) forming 1-methylsulfanyl-2-benzazepines in low yields (11–35%), whic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b42e564cee878133dc13010178fc46eb
https://doi.org/10.1007/s10593-021-02868-9
https://doi.org/10.1007/s10593-021-02868-9
Publikováno v:
Russian Chemical Bulletin. 65:1004-1007
Methyl (5-oxopyrazol-3-yl)acetate is added to methylthiocyanate C≡N bond in the presence of Ni(OAc)2 giving a corresponding heterocyclic N,S-ketene acetal. The latter compound was used as a convenient synthon in the synthesis of new pyrazolo[4,3-c]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f4085b5df71c08f9ef809f338abdf4c
https://doi.org/10.1007/s11172-016-1403-2
https://doi.org/10.1007/s11172-016-1403-2
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Tatyana S. Vshivkova, Yu. V. Shklyaev
Publikováno v:
Russian Journal of Organic Chemistry. 50:376-380
Podands containing 3,4-dihydroisoquinoline fragments were synthesized by reactions of 1,1′-{ethane-1,2-diylbis[oxy(3-methoxybenzene-4,1-diyl)]}bis(2-methylpropan-1-ol) and 1-(2-ethoxyethoxy)-2-methoxy-4-(2-methylprop-1-en-1-yl)benzene with ethyl cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::791884dabd89536d81c83aa219cb45e4
https://doi.org/10.1134/s1070428014030130
https://doi.org/10.1134/s1070428014030130
Publikováno v:
Theoretical Chemistry Accounts. 135
Here we report the results of a theoretical study devoted to the family of methyl thiocyanate (CH3–SCN) isomers. From among 14 species sharing the C2H3NS stoichiometry, the most thermodynamically stable of these are methyl isothiocyanate (CH3–NCS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de63ec831f1c2194fac407a8ee1a2e42
https://doi.org/10.1007/s00214-016-1978-6
https://doi.org/10.1007/s00214-016-1978-6
Publikováno v:
Russian Chemical Bulletin. 61:1627-1630
A number of dihydroisoquinolines were synthesized by the reaction of apiol, a natural allylbenzene, with nitriles. When methyl thiocyanate was used as the nitrile component, the formation of 2-azaspiro[4.5]deca-1,6,9-trien-8-one derivatives, the spir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dccdfffc24ed41c5a6f5cf07a74b0e1
https://doi.org/10.1007/s11172-012-0217-0
https://doi.org/10.1007/s11172-012-0217-0
Publikováno v:
Russian Journal of Organic Chemistry. 47:1428-1431
In the recent years 2-azaspiro[4.5]deca-1,6,9-trien8-one derivatives have attracted researchers’ attention due to their biological activity [1, 2]. These compounds may be synthesized in different ways; for example, 7-methoxy-2-methyl-2-azaspiro[4.5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49ff5fe3f67b91e7b5098a8688ad3531
https://doi.org/10.1134/s1070428011090284
https://doi.org/10.1134/s1070428011090284