Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mmakwena M. Mmonwa"'
Autor:
Mmakwena M. Mmonwa, Malose J. Mphahlele, Morad M. El-Hendawy, Ahmed M. El-Nahas, Nobuaki Koga
Publikováno v:
Molecules, Vol 19, Iss 7, Pp 9712-9735 (2014)
Iodine-catalyzed condensation of 2-amino-3,5-dibromobenzamide with cyclohexane-1,3-dione derivatives in refluxing toluene afforded the corresponding bisquinazolinones. Suzuki-Miyaura cross-coupling of the latter with arylboronic acids afforded tetraa
Externí odkaz:
https://doaj.org/article/b1ccc75b19264adabb72d29eaf4fafda
Publikováno v:
Molecules, Vol 22, Iss 7, p 1099 (2017)
A series of novel N-((2,5-diaryl-3-trifluoroacetyl)-1H-indol-7-yl)acetamides has been prepared via a successive and one-pot reaction sequence involving initial trifluoroacetic acid-mediated Beckmann rearrangement of the oximes derived from the 1-(2,5
Externí odkaz:
https://doaj.org/article/4b33b6e8d9cb4dd78634efd8406739ec
Publikováno v:
Organicbiomolecular chemistry. 17(8)
A simple and efficient method for the one-pot synthesis of novel 6-oxo-6H-pyrrolo[3,2,1-ij]quinoline-1,5-dicarbaldehydes via the Vilsmeier–Haack reaction of the corresponding 7-acetyl-2-arylindoles has been developed. The mechanism of this reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e58fa285eb24fc26cb0f161433ad1be
https://pubmed.ncbi.nlm.nih.gov/30720831
https://pubmed.ncbi.nlm.nih.gov/30720831
Publikováno v:
Emerging Trends in Chemical Sciences ISBN: 9783319604077
2-Amino-5-bromo-3-iodoacetophenone and 2-amino-5-bromo-3-iodobenzamide represent important synthons for the design and synthesis of various nitrogen-containing heterocyclic compounds and their annulated derivatives. We have demonstrated that these ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::775dfb84bbf91fe7d92e4f214228c581
https://doi.org/10.1007/978-3-319-60408-4_23
https://doi.org/10.1007/978-3-319-60408-4_23
Autor:
Morad M. El-Hendawy, Ahmed M. El-Nahas, Malose J. Mphahlele, Mmakwena M. Mmonwa, Nobuaki Koga
Publikováno v:
Molecules, Vol 19, Iss 7, Pp 9712-9735 (2014)
Molecules
Volume 19
Issue 7
Pages 9712-9735
Molecules
Volume 19
Issue 7
Pages 9712-9735
Iodine-catalyzed condensation of 2-amino-3,5-dibromobenzamide with cyclohexane-1,3-dione derivatives in refluxing toluene afforded the corresponding bisquinazolinones. Suzuki-Miyaura cross-coupling of the latter with arylboronic acids afforded tetraa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::810907b559a87ad5141ba09cb50f6503
https://doi.org/10.3390/molecules19079712
https://doi.org/10.3390/molecules19079712
Publikováno v:
Bioorganicmedicinal chemistry. 24(19)
A series of novel 2,5,7-tricarbo-substituted indoles were prepared via sequential Sonogashira and Suzuki-Miyaura cross-coupling of 2-amino-5-bromo-3-iodoacetophenone with terminal acetylenes and aryl/styrylboronic acids followed by palladium chloride
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e61d4fdceb325b3463b94da6c4181f10
https://pubmed.ncbi.nlm.nih.gov/27499368
https://pubmed.ncbi.nlm.nih.gov/27499368
Publikováno v:
International Journal of Molecular Sciences, Vol 19, Iss 8, p 2232 (2018)
International Journal of Molecular Sciences
Volume 19
Issue 8
International Journal of Molecular Sciences
Volume 19
Issue 8
A series of indole-aminoquinazolines was prepared via amination of the 2-aryl-4-chloroquinazolines with the 7-amino-2-aryl-5-bromoindoles. It was then evaluated for cytotoxicity in vitro against human lung cancer (A549), epithelial colorectal adenoca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::932cc640ade8d1872875390fec6fa4cd
https://doi.org/10.3390/ijms19082232
https://doi.org/10.3390/ijms19082232