A Facile Synthesis of Stentorin, the Photoreceptor of Stentor coeruleus
摘要:
Stentorin, a protozoan photoreceptor, was effectively synthesized via the Ullmann coupling reaction of 5-bromo-2-isopropyl-1,3,6,8-tetramethoxyanthraquinone which was prepared from 3-iso-propyl-2,4-dimethoxy-6-(3,5-dimethoxybenzyl)benzoic acid via intramolecular Friedel-Crafts reaction and regioselective bromination.
Syntheses, constitutions and properties of stentorin and isostentorin
摘要:
Stentorin and Isostentorin were synthesized from 2-isopropyl-1,3,6,8-tetrahydroxyanthrone by dimerization and chromatographic separation of the resulting regioisomers. The anthrone was prepared in four steps starting from easily available properly substituted benzene derivatives; the overall yield of the stentorins was 11%. The constitutions of stentorin and isostentorin could be unequivocally assigned from the H-1 NMR spectra of their potassium salts and were found to be in agreement with those derived recently by means of a rational synthesis. The spectroscopic, dissociation, and acid-base properties in ground and excited states as well as the chiroptical properties of the human serum albumin complexes were investigated and discussed comparing them with respective data of hypericin, fringelite D, and the natural Stenter pigment.
A Facile Synthesis of Stentorin, the Photoreceptor of Stentor coeruleus
作者:H Iio
DOI:10.1016/00404-0399(50)11425-
日期:1995.8.14
Stentorin, a protozoan photoreceptor, was effectively synthesized via the Ullmann coupling reaction of 5-bromo-2-isopropyl-1,3,6,8-tetramethoxyanthraquinone which was prepared from 3-iso-propyl-2,4-dimethoxy-6-(3,5-dimethoxybenzyl)benzoic acid via intramolecular Friedel-Crafts reaction and regioselective bromination.
Syntheses, constitutions and properties of stentorin and isostentorin
作者:H. Falk、E. Mayr
DOI:10.1007/bf00807060
日期:1995.12
Stentorin and Isostentorin were synthesized from 2-isopropyl-1,3,6,8-tetrahydroxyanthrone by dimerization and chromatographic separation of the resulting regioisomers. The anthrone was prepared in four steps starting from easily available properly substituted benzene derivatives; the overall yield of the stentorins was 11%. The constitutions of stentorin and isostentorin could be unequivocally assigned from the H-1 NMR spectra of their potassium salts and were found to be in agreement with those derived recently by means of a rational synthesis. The spectroscopic, dissociation, and acid-base properties in ground and excited states as well as the chiroptical properties of the human serum albumin complexes were investigated and discussed comparing them with respective data of hypericin, fringelite D, and the natural Stenter pigment.