论文信息 - Tautomerism and stereochemistry of hypericin: Force field, NMR, and X-ray crystallographic investigations - 字舞流文

Tautomerism and stereochemistry of hypericin: Force field, NMR, and X-ray crystallographic investigations

H. Falk | U. Wagner | Christoph Etzlstorfer | N. Müller | W. Schmitzberger | C. Etzlstorfer | Wolfgang Schmitzberger

[1] H. Falk,et al. Tautomerism and stereochemistry of dihydroxyperylenequinones: Force field investigations , 1993 .

[2] H. Falk,et al. On the nature of “soluble” hypericin inHypericum species , 1992 .

[3] R. Riccio,et al. The gymnochromes: novel marine brominated phenanthroperylenequinone pigments from the stalked crinoid Gymnocrinus richeri , 1991 .

[4] H. Falk,et al. A synthesis of emodin anthrone , 1991 .

[5] Felix T. Hong,et al. Molecular Electronics: Biosensors and Biocomputers , 1989 .

[6] D. Meruelo,et al. Therapeutic agents with dramatic antiretroviral activity and little toxicity at effective doses: aromatic polycyclic diones hypericin and pseudohypericin. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[7] Norman L. Allinger,et al. The MMP2 calculational method , 1987 .

[8] M. Randic,et al. Graph theoretical approach to local and overall aromaticity of benzenenoid hydrocarbons , 1975 .

[9] H. Brockmann,et al. Die konstitution des Pseudohypericins , 1975 .

[10] A. Camerman,et al. The crystal and molecular structure of perylene , 1964, Proceedings of the Royal Society of London. Series A. Mathematical and Physical Sciences.

[11] R. H. Thomson. Naturally occurring quinones , 1957 .