Zobrazeno 1 - 10
of 48
pro vyhledávání: '"MAKOTO KIRISAWA"'
Publikováno v:
ChemInform. 23
Negatively-charged cyclophanes ( 2a,2b ) having eight carboxylate groups on the aromatic rings were designed and synthesized. It is shown that they work as hosts that form inclusion complexes selectively with positively-charged aromatic compounds as
Publikováno v:
ChemInform. 24
A water-soluble cyclophane (9) having eight carboxyl groups that are attached to the aromatic rings via a spacer (-CH2SCH2-) was designed and synthesized. By 1H NMR spectral analysis, it is shown that 9 forms inclusion complexes in particular geometr
Publikováno v:
ChemInform. 25
Publikováno v:
ChemInform. 26
Publikováno v:
Tetrahedron Letters. 32:7295-7298
Negatively-charged cyclophanes ( 2a,2b ) having eight carboxylate groups on the aromatic rings were designed and synthesized. It is shown that they work as hosts that form inclusion complexes selectively with positively-charged aromatic compounds as
Autor:
Kazuo Uchikura, Makoto Kirisawa
Publikováno v:
Chemistry Letters. 20:1373-1376
A system for electrogenerated chemiluminescence based on the reaction of electrogenerated Ru(bpy)33+ with tryptophan (Trp) is described. The orange chemiluminescence was generated by reaction of Ru(bpy)33+ with Trp in acidic solution. The lowest dete
Publikováno v:
Chemical and Pharmaceutical Bulletin. 38:1447-1450
Panaxacol (1) and dihydropanaxacol (2), cytotoxic polyacetylenes isolated from the callus of Panax ginseng, were synthesized starting from D-(-)-diethyl tartrate. The absolute configuration of 1 was determined to be 9R, 10R and the absolute configura
Publikováno v:
Analytical Sciences. 9:121-123
Publikováno v:
Chemical and Pharmaceutical Bulletin. 41:1211-1213
Novel cyclophanes (9a, b) having eight carboxyl groups on the aromatic rings were designed and synthesized. Macrocyclization of 7a and 7b with 6 was carried out under a high dilution condition to give the corresponding 8a and 8b in 23% and 28% yields
Publikováno v:
Phytochemistry. 31:3499-3501
Two new C 17 -polyacetylenes and a C 14 -polyacetylene were isolated from dried roots of Panax quinquefolium . Their structures were determined by their 1 H NMR, 13 C NMR and mass spectral data. The cytotoxic activity of C 17 -polyacetylenes against