Zobrazeno 1 - 10
of 33
pro vyhledávání: '"G. Loloiu"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 38:242-248
The Krohnke reaction of 2ω-bromoacetylphenoxathiin and 2-ω-bromophenoxathiin 10,10-dioxide, through N-ylide and S-ylide intermediates, leading to the corresponding glyoxals, was described. The condensation reaction of 2-ω-bromoacetylphenoxathiin w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec6e365e48f28e6471b5cd5d1a96e25d
https://doi.org/10.1023/a:1015307813291
https://doi.org/10.1023/a:1015307813291
Publikováno v:
Chemistry of Heterocyclic Compounds. 37:353-359
Reactions of α-bromoacetylphenoxathiin, α-bromoacetylphenoxathiin 10,10-dioxide, or α-bromoacetylthianthrene with certain p-(arylsulfonyl)thiobenzamides lead to the formation of the corresponding 2,4-disubstituted thiazoles. The new compounds were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c45bdc660a627fb9c5c456c2b569c3f3
https://doi.org/10.1023/a:1017567302267
https://doi.org/10.1023/a:1017567302267
Publikováno v:
Chemistry of Heterocyclic Compounds. 35:1474-1479
The reactions of phenoxathiin-2-carbonyl-or thianthrene-2-carbonyl-isothiocyanates with certain primary amines lead to the formation of corresponding N′-substituted-N-hetaroylthiocarbamides. The aforementioned isothiocyanates were obtained in situ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3be8c0293830fa96c435389121797db8
https://doi.org/10.1007/bf02251824
https://doi.org/10.1007/bf02251824
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:866-869
Benzoylation of phenoxathiin leads to a mixture of 2- and 3-benzoylphenoxathiins. Starting from 3-phenoxathiincarbonyl chloride and benzene in the presence of anhydrous aluminum chloride, 2-benzoylphenoxathiin was obtained instead of the 3-substitute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f39ec652d26e15f980b5d6e71e73c7d
https://doi.org/10.1007/bf02251698
https://doi.org/10.1007/bf02251698
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:363-366
The title compound was obtained using the Sandmeyer reaction starting from 2-aminophenoxathiine. A new synthesis of N-methylpyrrolo[2,3-b]phenoxathiin-2,3-dione was also presented. Chemical and spectral data supporting the structure of the newly synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69da6d15f2a5daf7f68f353969b45c63
https://doi.org/10.1007/bf02290733
https://doi.org/10.1007/bf02290733
Publikováno v:
ChemInform. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fbe7daed576aeb9a77604e900d07278
https://doi.org/10.1002/chin.199745166
https://doi.org/10.1002/chin.199745166
Publikováno v:
ChemInform. 29
The title compound was obtained using the Sandmeyer reaction starting from 2-aminophenoxathiine. A new synthesis of N-methylpyrrolo[2,3-b]phenoxathiin-2,3-dione was also presented. Chemical and spectral data supporting the structure of the newly synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a91bb0bda3dbabd27507a3cdeb50379
https://doi.org/10.1002/chin.199838169
https://doi.org/10.1002/chin.199838169
Publikováno v:
ChemInform. 31
The reactions of phenoxathiin-2-carbonyl-or thianthrene-2-carbonyl-isothiocyanates with certain primary amines lead to the formation of corresponding N′-substituted-N-hetaroylthiocarbamides. The aforementioned isothiocyanates were obtained in situ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::568071e804eaad54062cb8166614f5d3
https://doi.org/10.1002/chin.200036160
https://doi.org/10.1002/chin.200036160
Publikováno v:
ChemInform. 33
Reactions of α-bromoacetylphenoxathiin, α-bromoacetylphenoxathiin 10,10-dioxide, or α-bromoacetylthianthrene with certain p-(arylsulfonyl)thiobenzamides lead to the formation of the corresponding 2,4-disubstituted thiazoles. The new compounds were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d31cd62b9b771a00c8b20e8ee175d8c
https://doi.org/10.1002/chin.200201125
https://doi.org/10.1002/chin.200201125
Publikováno v:
ChemInform. 33
The Krohnke reaction of 2ω-bromoacetylphenoxathiin and 2-ω-bromophenoxathiin 10,10-dioxide, through N-ylide and S-ylide intermediates, leading to the corresponding glyoxals, was described. The condensation reaction of 2-ω-bromoacetylphenoxathiin w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f52099172fce269f8fd0a12ff644694
https://doi.org/10.1002/chin.200242167
https://doi.org/10.1002/chin.200242167