Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ya. V. Zachinyaev"'
Publikováno v:
Chemistry of Heterocyclic Compounds. 46:1471-1475
The reaction of 2,2-dimethyl-1,2-dihydrobenzo[f]isoquinoline with malonic acid gave (2,2-dimethyl-1,2,3,4-tetrahydrobenzo[f]isoquinolin-4-yl)acetic acid, the acid chloride of which readily forms esters with alcohols and phenols. Reaction of the same
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a8d87e7159aa168db694ac19ccb9951
https://doi.org/10.1007/s10593-011-0694-3
https://doi.org/10.1007/s10593-011-0694-3
Publikováno v:
Russian Journal of Applied Chemistry. 82:1321-1323
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6adcdd8ab6c337125339508b9247cc3d
https://doi.org/10.1134/s1070427209070313
https://doi.org/10.1134/s1070427209070313
Publikováno v:
ChemInform. 42
The reaction of 2,2-dimethyl-1,2-dihydrobenzo[f]isoquinoline with malonic acid gave (2,2-dimethyl-1,2,3,4-tetrahydrobenzo[f]isoquinolin-4-yl)acetic acid, the acid chloride of which readily forms esters with alcohols and phenols. Reaction of the same
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d195fb9544d7bbe280b7f136b988e56
https://doi.org/10.1002/chin.201139143
https://doi.org/10.1002/chin.201139143
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87e26c7982aebf9f1ef33229983be220
https://doi.org/10.1002/chin.199145165
https://doi.org/10.1002/chin.199145165
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e682b0200af8b08898c48170224858ae
https://doi.org/10.1002/chin.199337203
https://doi.org/10.1002/chin.199337203
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a55ebe28be68c91ea6f66717fabb205
https://doi.org/10.1002/chin.199420111
https://doi.org/10.1002/chin.199420111
Autor:
A. I. Bobrov, Ya. V. Zachinyaev
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92bc724fc325e1ceab7112e5b752ddc7
https://doi.org/10.1002/chin.199439178
https://doi.org/10.1002/chin.199439178
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6217b619e44104bf8a7ac8587a69618
https://doi.org/10.1002/chin.199603100
https://doi.org/10.1002/chin.199603100
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef6449c1f8f10c5cf889b11b101ec0e0
https://doi.org/10.1002/chin.199647071
https://doi.org/10.1002/chin.199647071
Publikováno v:
Chemistry of Heterocyclic Compounds. 28:104-107
The reaction of 2-mercaptobenzimida(thia)zole with 1,4-naphthoquinone proceeds as nucleophilic 1,4-addition to give the corresponding thioethers. The reaction of 1,4-naphthoquinone oxide with 2-mercaptobenzimidazole leads to benzimidazonaphthothiazol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::133a43a4b01904d8ed05a70fbbf6fb69
https://doi.org/10.1007/bf00529492
https://doi.org/10.1007/bf00529492