Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Eugen Eichenberger"'
Publikováno v:
CHIMIA, Vol 45, Iss 1-2 (1991)
The synthesis of the binuclear 'RuII-CoII' complex (5a) is described. Its two subunits consist of derivatives of RuII(bpy)3++ and cob(II)yrinate. 5a undergoes 7 one-electron redox processes in the potential range + 1.5 to–1.8 V (vs. SCE). Luminesc
Externí odkaz:
https://doaj.org/article/2688d75cc29640c0a899af7b9abdc9d8
Publikováno v:
Tetrahedron Letters. 35:6623-6626
Intramolecular hydrogen transfer reactions of 3-O-acyl-α-methyl- d -mannopyranosides occur in a 1,6-fashion to give inverted β-mannopyranosides. The yields are limited by competing 1,5-hydrogen transfer reactions that give isomeric α-glucopyranosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bc18db6c7ae5c04a7c63ea2a9a03604
https://doi.org/10.1016/s0040-4039(00)73451-4
https://doi.org/10.1016/s0040-4039(00)73451-4
Publikováno v:
Journal of the American Chemical Society. 116:4279-4288
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88b62ac19762a259900e45d2d816090a
https://doi.org/10.1021/ja00089a017
https://doi.org/10.1021/ja00089a017
Publikováno v:
ChemInform. 24
The elimination of thiocyanic acid from the stereoisomers of the hex-3-ene-2,5-diyl dithiocyanates, 4a, 4b, 6a and 6b, in the presence of a strong neutral base in an organic solvent, yields mixtures of the hex-2,4-dien-2-yl thiocyanates 9, 10 and 11v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a4e0ff5c8cec22d630f5a81b7b493b8
https://doi.org/10.1002/chin.199324079
https://doi.org/10.1002/chin.199324079
Publikováno v:
ChemInform. 26
Intramolecular hydrogen transfer reactions of 3-O-acyl-α-methyl- d -mannopyranosides occur in a 1,6-fashion to give inverted β-mannopyranosides. The yields are limited by competing 1,5-hydrogen transfer reactions that give isomeric α-glucopyranosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3fab34b6fa74f7b9a05d6c5658f1076
https://doi.org/10.1002/chin.199505255
https://doi.org/10.1002/chin.199505255
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d49e2395881099c6511085a5c7ae4666
https://doi.org/10.1002/chin.199440060
https://doi.org/10.1002/chin.199440060
Publikováno v:
Photochemistry and Photobiology. 52:283-292
— Dihydropyridinones (DHP) react photochemically with olefins to form cycloaddition products. The reactions proceed through the lowest excited state T1 of the DHPs, with rate constants which depend on the olefin and can approach the diffusional lim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71d61cbbc52eaf15fe9865d79a9b1962
https://doi.org/10.1111/j.1751-1097.1990.tb04183.x
https://doi.org/10.1111/j.1751-1097.1990.tb04183.x
The stereochemistry of the 1,4-elimination of thiocyanic acid from hex-3-ene-2,5-diyl dithiocyanates
Publikováno v:
Journal of the Chemical Society, Chemical Communications. :246
The elimination of thiocyanic acid from the stereoisomers of the hex-3-ene-2,5-diyl dithiocyanates, 4a, 4b, 6a and 6b, in the presence of a strong neutral base in an organic solvent, yields mixtures of the hex-2,4-dien-2-yl thiocyanates 9, 10 and 11v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a17e522c76fdf2e466f87e7219d3fa4
https://doi.org/10.1039/c39930000246
https://doi.org/10.1039/c39930000246