215385-40-3Relevant academic research and scientific papers
First Friedel-Crafts diacylation of a phenanthrene as the basis for an efficient synthesis of nonracemic [7]helicenes
Paruch,Katz,Incarvito,Lam,Rhatigan,Rheingold
, p. 7602 - 7608 (2007/10/03)
Reported are the first examples of Friedel-Crafts reactions used to prepare 3,6-diacylphenanthrenes. 9,10-Dimethoxyphenanthrene gives its 3,6-diacetyl derivative in good yield and in large amounts. The ketone's triisopropylsilyl enol ether when combined with 1,4-benzoquinone forms a [7]helicenebisquinone. This bisquinone's reduction product, a bishydroquinone, when combined with methanolic HCl gives the [7]helicene whose peripheral side chains are all methoxyls but whose interior hydroxyls remain. The diastereomeric (1S)-(-)-camphanates can be separated by crystallization. Their structures, analyzed by X-ray diffraction, demonstrate that the camphanates' lactone functions point away from the ring system when the helicene has the (P) configuration and toward it when the helicene has the (M) configuration. This is because the camphanates' O=C-C-O dihedral angles are, as expected, close to 0°in the former and close to 180°in the latter. Other derivatives of 3,6-diacetylphenanthrene and of [7]helicenebisquinone are prepared, and the crystal structure of one of the latter is analyzed.
Efficient synthesis of functionalized [7]helicenes
Fox, Joseph M.,Goldberg, Naomi R.,Katz, Thomas J.
, p. 7456 - 7462 (2007/10/03)
[7]Helicenebisquinones can be made easily and in quantity by reacting the silyl enol ethers of a 9,10-dialkoxy-, or better a 9,10-disiloxy-, 3,6-diacetylphenanthrene, with p-benzoquinone. If an ethyl enol ether is used in place of the silyl enol ether, the transformation proceeds in much lower yield. The [7]helicenes are efficiently resolved into their enantiomers, and absolute configurations are assigned.
