Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Judith J. Bischoff"'
Publikováno v:
Journal of the American Institute for Conservation. 40:268
Publikováno v:
Studies in Conservation. 40:207
Publikováno v:
Studies in Conservation. 39:284
Autor:
Judith J. Bischoff, David Erhardt
Publikováno v:
Studies in Conservation. 39:3
Mixtures that contain one or more of some common components of aqueous resin soap cleaning mixtures—organic resin or bile acids, an amine that is used to form the acid salt (soap), and a gelling agent—were prepared in order to determine the contr
Publikováno v:
Journal of the American Chemical Society. 108:7773-7778
On determine la reactivite de la dimethyl-2',6' phenyl-10 ethyl-5 hydroperoxy-4a methyl-3 isoalloxazine vis-a-vis des thioanisoles p-substitues, des alkyl phenyl sulfures, des dialkyl sulfures et des benzyl butyl amines
Autor:
Judith J. Bischoff, Audrey Miller
Publikováno v:
Synthesis. 1986:777-779
Conversion par reaction avec des amides d'acides sulfoformimidiques. Obtention des acides guanidino-2 alcanoiques
Publikováno v:
ChemInform. 18
On determine la reactivite de la dimethyl-2',6' phenyl-10 ethyl-5 hydroperoxy-4a methyl-3 isoalloxazine vis-a-vis des thioanisoles p-substitues, des alkyl phenyl sulfures, des dialkyl sulfures et des benzyl butyl amines
Publikováno v:
Chemical research in toxicology. 1(3)
The reactions of aminoiminomethanesulfonic acid, phenylaminoiminomethanesulfonic acid, and N,N'-diphenylaminoiminomethanesulfonic acid in aqueous media at pH 7.4, 10, and 13-14 were investigated. At neutral pH hydrolysis to the corresponding urea was
Autor:
Audrey Miller, Judith J. Bischoff
Publikováno v:
ChemInform. 18
Conversion par reaction avec des amides d'acides sulfoformimidiques. Obtention des acides guanidino-2 alcanoiques
Autor:
Audrey Miller, Judith J. Bischoff
Publikováno v:
Biological Reactive Intermediates III ISBN: 9781468451368
Thiourea and some monosubstituted thioureas are toxic and tumorogenic while 1,3-diarylthioureas are not. There are strong indications that the biological activity of these compounds is due to oxidation at sulfur followed by reactions in which the sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::888cbb5a31ea4a35add81465b263abb4
https://doi.org/10.1007/978-1-4684-5134-4_89
https://doi.org/10.1007/978-1-4684-5134-4_89