155500-22-4Relevant academic research and scientific papers
Successive Michael reaction-sigmatropic rearrangement of naphthodiquinone with O-silylated ketene acetals leading to synthesis of cycloshikonin and structure-reactivity relationship for side chain of naphthazarins
Aso,Kanematsu
, p. 1549 - 1556 (1993)
Synthesis of cycloshikonin via successive Michael reaction-sigmatropic rearrangement of naphthodiquinone with O-silylated ketene acetals is described. The structure dependence of the reactivity of the side chain of intermediary naphthazarin derivatives ha
