Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Alexander Purtsas"'
Publikováno v:
Molecules, Vol 25, Iss 7, p 1608 (2020)
We describe the synthesis and photophysical properties of tetraarylnaphthidines. Our synthetic approach is based on an iron-catalyzed oxidative C–C coupling reaction as the key step using a hexadecafluorinated iron–phthalocyanine complex as a cat
Externí odkaz:
https://doaj.org/article/e6582865f2c543abbb50ec62ab7aa5fe
Publikováno v:
Chemistry – A European Journal. 28
We describe the oxygenation of tertiary arylamines, and the amination of tertiary arylamines and phenols. The key step of these coupling reactions is an iron-catalyzed oxidative C-O or C-N bond formation which generally provides the corresponding pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7850d4bbbba6e4a8475258236ef206d
https://doi.org/10.1002/chem.202104292
https://doi.org/10.1002/chem.202104292
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
A mild procedure for the oxidative C−C cross‐coupling of tertiary anilines with phenols is described which provides the products generally in high yields and with excellent selectivity. The reaction is catalyzed by the hexadecafluorinated iron–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::808f704bebf46ddc0508683f26a6f828
https://doi.org/10.1002/chem.201905595
https://doi.org/10.1002/chem.201905595
Publikováno v:
Molecules
Volume 25
Issue 7
Molecules, Vol 25, Iss 1608, p 1608 (2020)
Volume 25
Issue 7
Molecules, Vol 25, Iss 1608, p 1608 (2020)
We describe the synthesis and photophysical properties of tetraarylnaphthidines. Our synthetic approach is based on an iron-catalyzed oxidative C&ndash
C coupling reaction as the key step using a hexadecafluorinated iron&ndash
phthalocyanin
C coupling reaction as the key step using a hexadecafluorinated iron&ndash
phthalocyanin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68351273ebb27fe9d9faf5efccad7572