Zobrazeno 1 - 8
of 8
pro vyhledávání: '"B. A. Rekhter"'
Autor:
M. A. Rekhter, B. A. Rekhter
Publikováno v:
Chemistry of Heterocyclic Compounds. 48:386-389
The experimental discovery of a significant modification of a chemical reaction has always been considered a noteworthy achievement. As shown below, four modifications of the indolinedione-indole rearrangement and three modifications of the synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ea6a26e214bd05677d781aa1f93c860
https://doi.org/10.1007/s10593-012-1005-3
https://doi.org/10.1007/s10593-012-1005-3
Autor:
M. A. Rekhter, B. A. Rekhter
Publikováno v:
Chemistry of Heterocyclic Compounds. 46:1161-1164
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a6fe5fbbcf7059400a1090fa8a83e72
https://doi.org/10.1007/s10593-010-0649-0
https://doi.org/10.1007/s10593-010-0649-0
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a64205d578a2a6dd25a7276a1f4eb84
https://doi.org/10.1002/chin.199832150
https://doi.org/10.1002/chin.199832150
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2fc83e66ed661ebb37b41b903cb3df9
https://doi.org/10.1002/chin.199838118
https://doi.org/10.1002/chin.199838118
Autor:
M. A. Rekhter, B. A. Rekhter
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f54f959b3a0bd35da12ba52e53775a13
https://doi.org/10.1002/chin.199841116
https://doi.org/10.1002/chin.199841116
Autor:
M. A. Rekhter, B. A. Rekhter
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:499-501
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ff16708ab02a9a40681435bc706e914
https://doi.org/10.1007/bf02290895
https://doi.org/10.1007/bf02290895
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:275-277
Only the bromine atom at the primary carbon atom participates in nucleophilic replacement by a trifluoroacetate ion and elimination of HBr in 1-(2,3-dibromopropyl)isatin.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f38d748fc145e4cda3f9e4ca7bddd51c
https://doi.org/10.1007/bf02290716
https://doi.org/10.1007/bf02290716
Publikováno v:
Chemistry of Heterocyclic Compounds. 34:250-251
l-(2-Oxoalkyl)indole-2,3-diones (la-f) undergo the indoledione-indole rearrangement in 0.4-1% aq. NaOH to give the sodium salt of the corresponding 2-(l-oxoalkyl)indole-3-carboxylic (Ila-f) [1-4]. Under the same conditions, only opening of the hetero
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd159d3cdb6bc97e23e2b8e0a8e0cee4
https://doi.org/10.1007/bf02315194
https://doi.org/10.1007/bf02315194