Synthesis and Antimicrobial/Cytotoxic Assessment of Ferrocenyl Oxazinanes, Oxazinan-2-ones, and Tetrahydropyrimidin-2-ones
Author(s) -
Rastko D. Vukićević,
Matthias D’hooghe,
Anka Pejović,
Barbara Danneels,
Tom Desmet,
Ba Thi Cham,
Tuyen Van Nguyen,
Niko S. Radulović
Publication year - 2015
Publication title -
synlett
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.712
H-Index - 133
eISSN - 1437-2096
pISSN - 0936-5214
DOI - 10.1055/s-0034-1380348
Subject(s) - chemistry , antimicrobial , ferrocene , combinatorial chemistry , organic chemistry , cytotoxic t cell , biochemistry , in vitro , electrochemistry , electrode
3-Arylamino-1-ferrocenylpropan-1-ones, prepared through aza-Michael addition of aromatic amines to 1-ferrocenylpropenone, were transformed into the corresponding 1,3-amino alcohols upon NaBH4-mediated carbonyl reduction. The latter amino alcohols were deployed as eligible substrates for the synthesis of a variety of ferrocene-containing heterocycles including 1,3-oxazinanes, 1,3-oxazinan-2-ones, and tetrahydropyrimidin-2-ones, which were subsequently evaluated for their antimicrobial and cytotoxic activities
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