作者:Donald W. Cameron、Pauline J. de Bruyn
DOI:10.1016/s0040-4039(00)61155-3
日期:1992.9
Tetracenomycins D, A2, B1 and B2 (2)-(5) have been synthesised for the first time, by an efficient, regioselective sequence based on cycloaddition methodology; the ambiguity that existed for tetracenomycins B1 and B2 has thereby been resolved in favour of structures (4a) and (5b) respectively.