1.
Biosci Biotechnol Biochem
; 81(8): 1466-1469, 2017 Aug.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28508733
RESUMO
The synthesis of aurachin B, an antibiotic that features a C3-oxygen-substituted quinoline N-oxide nucleus bearing a farnesyl side chain at C4, was accomplished in 60% overall yield from o-nitrotoluene by a concise five-step sequence. An enantioselective synthesis of aurachin H was also achieved for the first time in only two steps from an optically active epoxy iodide.