Zobrazeno 1 - 10
of 13
pro vyhledávání: '"T. I. Chudakova"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 52:267-274
N-(Chlorosulfonyl)imidoyl chlorides react regioselectively with anilines, 2-aminomethylnaphthaline, or 1,2,3,4-tetrahydroquinoline leading to derivatives of 1,2,4-benzothiadiazine 1,1-dioxide. Heterocyclization occurs at the sterically less hindered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fc402af964ac8e578e0dfcb389f2c85
https://doi.org/10.1007/s10593-016-1873-z
https://doi.org/10.1007/s10593-016-1873-z
Publikováno v:
ChemInform. 47
N-(Chlorosulfonyl)imidoyl chlorides react regioselectively with anilines, 2-aminomethylnaphthaline, or 1,2,3,4-tetrahydroquinoline leading to derivatives of 1,2,4-benzothiadiazine 1,1-dioxide. Heterocyclization occurs at the sterically less hindered
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c302359651b6a57d9d1c030fc8c0c9a
https://doi.org/10.1002/chin.201646188
https://doi.org/10.1002/chin.201646188
Publikováno v:
Russian Journal of General Chemistry. 79:195-199
N-Hydroxyfluorobenzimidoylphosphonates and their O-acyl derivatives are synthesized. Reaction of phosphorylated oximes with sulfinyl chloride proceeds with rearrangement and leads to synthetically prospective N-sulfonylimidoylphosphonates. By the met
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f46d951331a7bc987d57eaa55ef2091f
https://doi.org/10.1134/s1070363209020054
https://doi.org/10.1134/s1070363209020054
Autor:
Petro P. Onys’ko, T. I. Chudakova, Yuliya V. Rassukana, Olena A. Suvalova, Anatolii D. Sinitsa
Publikováno v:
Tetrahedron Letters. 44:1855-1857
The reaction of alkyl trifluoro(organylsulfonylimino)propionates with phosphites occurs with NC transfer of the RSO2 group and leads to sulfonyl-substituted trifluoroalanine derivatives. The novel rearrangement is interpreted as cheletropic 1,4-cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e3719bf85757c97140eb7baf66b15b7
https://doi.org/10.1016/s0040-4039(03)00097-2
https://doi.org/10.1016/s0040-4039(03)00097-2
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d4975c2e0ce4e21995a62009b473a8a
https://doi.org/10.1002/chin.199118216
https://doi.org/10.1002/chin.199118216
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdd1b3683068d846320378e8c1023eb8
https://doi.org/10.1002/chin.199522231
https://doi.org/10.1002/chin.199522231
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfce9e0f17648cb0285a5a94f851c065
https://doi.org/10.1002/chin.199251232
https://doi.org/10.1002/chin.199251232
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbaa61aa84561d502416873c27a962db
https://doi.org/10.1002/chin.199051222
https://doi.org/10.1002/chin.199051222
Autor:
E. I. Kiseleva, Anatoly D. Sinitsa, Petro P. Onys’ko, T. V. Kim, E. A. Suvalova, T. I. Chudakova
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bcf601265622c305ea32d71d6eec199
https://doi.org/10.1002/chin.199016233
https://doi.org/10.1002/chin.199016233
Publikováno v:
Gigiena i sanitariia. (4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::29afd8467137a442355f98378f87ec39
https://pubmed.ncbi.nlm.nih.gov/2373402
https://pubmed.ncbi.nlm.nih.gov/2373402