作者:Kazuhiko Nakamura、Shigeru Nishiyama、Shosuke Yamamura
DOI:10.1016/0040-4039(95)01857-e
日期:1995.11
Preparation of the vancomycin analogs (SAV-1 and SAV-2) is described. The key step is construction of a bicyclic diaryl ether residue by means of thallium (III) oxidation of the corresponding halogenated phenols.