Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Carme Cantos Llopart"'
Autor:
Carme Cantos Llopart, John A. Joule
Publikováno v:
ARKIVOC, Vol 2004, Iss 10, Pp 20-38 (2004)
Externí odkaz:
https://doaj.org/article/7f1ce1739a2b445995c90aa8ed7d8e95
Publikováno v:
Canadian Journal of Chemistry. 82:1649-1661
1-Arylimidazol-2(1H)-ones are shown to be readily lithiated, using 2 mol equiv. of n-butyllithium, on the benzene ring, ortho to the heterocycle. 1-Aryl-4,5-dihydroimidazol-2(1H)-ones also undergo metalation on the aromatic substitutuent ortho to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1141deac5a856a8a1064427d82f06a6
https://doi.org/10.1139/v04-137
https://doi.org/10.1139/v04-137
Autor:
Juan-C. del Castillo, Rosa Griera, Joan Bosch, Carme Cantos-Llopart, Mercedes Amat, Joan Huguet
Publikováno v:
ChemInform. 37
A synthetic route to a new structural type of potential antibacterials, with a hybrid 3-aryltetrahydroisoquinoline-6,7-diol/N-aryloxazolidinone structure, is reported. The synthesis involves the successive construction of the 3-aryltetrahydroisoquino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b4252d705b44d76a9e8b299c3672d67
https://doi.org/10.1002/chin.200618138
https://doi.org/10.1002/chin.200618138
Publikováno v:
ChemInform. 36
1-Arylimidazol-2(1H)-ones are shown to be readily lithiated, using 2 mol equiv. of n-butyllithium, on the benzene ring, ortho to the heterocycle. 1-Aryl-4,5-dihydroimidazol-2(1H)-ones also undergo ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::251c53d5cc7ed46ec7623aab8206445e
https://doi.org/10.1002/chin.200529068
https://doi.org/10.1002/chin.200529068
Autor:
Rosa Griera, Mercedes Amat, Joan Bosch, Joan Huguet, Juan-C. del Castillo, Carme Cantos-Llopart
Publikováno v:
Bioorganicmedicinal chemistry letters. 15(10)
The synthesis of N-aryloxazolidinone 1, a conformationally constrained analog of linezolid embodying a tricyclic pyrrolo[1,2-a][4,1]benzoxazepine moiety as the N-aryl substituent, is reported. The synthetic route involves the successive construction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25312ad085dd0dc607cef46b0a5ec7d2
https://pubmed.ncbi.nlm.nih.gov/15863307
https://pubmed.ncbi.nlm.nih.gov/15863307