51850-49-8Relevant articles and documents
NMR study of naphthoflavones
Joseph-Nathan, P.,Santillan, R. L.
, p. 1077 - 1080 (1984)
The NMR spectra of α-, β- and γ-naphthoflavones were assigned at 25.2 MHz resorting to models such as the unsubstituted flavone and appropriate substituted acetylmethoxynaphthalenes.Supporting evidence for the assignments was provided by gated decoupled spectra and all the chemical shifts in the 11 compounds studied gave a self-consistent data set.
Divergent approach to the bisanthraquinone natural products: Total synthesis of (S)-bisoranjidiol and derivatives from binaphtho- para -quinones
Podlesny, Erin E.,Kozlowski, Marisa C.
, p. 466 - 476 (2013/03/13)
The development of the first asymmetric synthesis of a chiral anthraquinone dimer is outlined, resulting in the first total synthesis of (S)-bisoranjidiol. Rather than a biomimetic dimerization retrosynthetic disconnection, the anthracenyl ring systems ar
Regioselective hydrolysis of diacetoxynaphthalenes catalyzed by Pseudomonas sp. lipase in an organic solvent
Ciuffreda, Pierangela,Casati, Silvana,Santaniello, Enzo
, p. 317 - 321 (2007/10/03)
Depending on the relative positions of the acetyl groups in the aromatic rings, the Pseudomonas sp. lipase-catalyzed hydrolysis of diacetoxynaphthalenes in tert-butylmethyl ether proceeds regioselectively to afford the corresponding monoacetates.
