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Efficient syntheses of streptocarpone and (±)-a-dunnione
An efficient divergent synthesis of both streptocarpone and racemic α-dunnione from lawsone are described. A one-pot, formal [3+2] cyclization to form a furanonaphthoquinone directly provided a common intermediate.
Synthesis of Iodinated Naphthoquinones Using Morpholine-Iodine Complex
(Synthetic Communications Vol. 34, No. 18, pp. 3389–3397, 2004, 2004)
The efficient synthesis of 2‐hydroxy‐3‐iodo‐1,4‐naphthoquinone (3), 2‐amino‐3‐iodo‐1,4‐naphthoquinone (4), and 2‐iodo‐1,4‐naphthoquinone (5) have been developed using the parent naphthoquinone in combination with the ...
Neutral organic redox pairs based on sterically hindered hydroquinone/benzoquinone derivatives for dye-sensitized solar cells
Substituted derivatives of hydroquinone/benzoquinone were studied as organic redox mediators in the electrolyte for dye-sensitized solar cells (DSSCs). Thus, di-tert-butylhydroquinone (DTHQ), thymohydroquinone (ThymHQ) and ...
Crystal structure of (E)-2-(tert-butylamino)-4-(tertbutylimino)naphthalen-1(4H)-one
The title compound, C18H24N2O, is the first example of a naphthoquinone imine derivative isolated in the 4-imine/2-amine tautomeric form having bulky alkyl substituents at the N atoms. The molecular conformation is stabilized ...
Crystal structure of 4-[(adamantan-1-yl)amino]naphthalene-1,2-dione
The title compound, C20H21NO2, an example of a stable 1,2-naphthoquinone, was determined by single-crystal X-ray diffraction analysis at 100 K. This structure illustrates steric buttressing of the adamantanyl group, forcing ...