Zobrazeno 1 - 9
of 9
pro vyhledávání: '"T. S. Toth"'
Publikováno v:
Tetrahedron: Asymmetry. 4:339-344
Who hath his life from rumours freed, Whose conscience is his strong retreat; Whose state can neither flatterers feed, Nor ruin make accusers great; Who God doth late and early pray More of His grace than gifts to lend; And entertains the harmless da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2bfe3316ed4b4aa5f8d82dce61f8454
https://doi.org/10.1016/s0957-4166(00)86078-4
https://doi.org/10.1016/s0957-4166(00)86078-4
Autor:
T. S. Toth, Sándor Antus, Agnes Gottsegen, József Szunyog, T. Kovacs, Hildebert Wagner, Eszter Baitz-Gács
Publikováno v:
Liebigs Annalen der Chemie. 1993:105-109
The first synthesis of racemic silandrin (rac-1), which shows significant antihepatotoxic activity, has been accomplished via the key intermediate 9 prepared from the readily available starting materials caffeic acid ethyl ester (4) and coniferyl alc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::666690e71309906434d58a8f94ab4f82
https://doi.org/10.1002/jlac.199319930119
https://doi.org/10.1002/jlac.199319930119
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ac710c15ab9beadf5e72da168cd021b
https://doi.org/10.1002/chin.199139217
https://doi.org/10.1002/chin.199139217
Autor:
Eszter Baitz-Gács, Hildebert Wagner, T. S. Toth, József Szunyog, Sándor Antus, T. Kovacs, Agnes Gottsegen
Publikováno v:
ChemInform. 24
The first synthesis of racemic silandrin (rac-1), which shows significant antihepatotoxic activity, has been accomplished via the key intermediate 9 prepared from the readily available starting materials caffeic acid ethyl ester (4) and coniferyl alc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6e208846db2a5980d9081bd8cf2332d
https://doi.org/10.1002/chin.199324299
https://doi.org/10.1002/chin.199324299
ChemInform Abstract: Lipase-Catalyzed Kinetic Resolution of (.+-.)-2-Hydroxymethyl-1,4- benzodioxane
Publikováno v:
ChemInform. 24
Who hath his life from rumours freed, Whose conscience is his strong retreat; Whose state can neither flatterers feed, Nor ruin make accusers great; Who God doth late and early pray More of His grace than gifts to lend; And entertains the harmless da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adbce18cd6db16d55550f36dccfe3621
https://doi.org/10.1002/chin.199328084
https://doi.org/10.1002/chin.199328084
Publikováno v:
Liebigs Annalen der Chemie. 1991:633-641
Starting from cholesterol the three possible stereoisomeric 1,4-benzodioxanes 24, 31, 32 and a series of analogues with 2βH,3βH configuration (25–27, 29, 30) have been synthesized. The α band of the 1,4-benzodioxane chrompohore has been unequivo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e956d267251325185cb6598063d5705e
https://doi.org/10.1002/jlac.1991199101115
https://doi.org/10.1002/jlac.1991199101115
Publikováno v:
Die Naturwissenschaften. 91(10)
Tail autotomy in lizards is an adaptive strategy that has evolved to reduce the risk of predation. Since tail loss reduces body mass and moving ability-which in turn are expected to influence thermal balance-there is potential for a trade-off between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06ead677a230412fd5ab5973d7bf9818
https://pubmed.ncbi.nlm.nih.gov/15729762
https://pubmed.ncbi.nlm.nih.gov/15729762
Publikováno v:
Chemische Berichte. 122:1017-1019
The cis- and trans-tetrahydrodibenzo-1,4-dioxanes 2 and 3 were synthesized from 2-bromocyclohexanone in five steps.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1516e12a4f3f2a7306679017fac7b9bb
https://doi.org/10.1002/cber.19891220536
https://doi.org/10.1002/cber.19891220536
Publikováno v:
ChemInform. 20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cac0de0f23d8f9b17011109ce4385da8
https://doi.org/10.1002/chin.198933181
https://doi.org/10.1002/chin.198933181