✦ LIBER ✦

Biological potency of organic selenium compounds IV. Straight-chain dialkylmono- and diselenides

✍ Scribed by Klaus Schwarz; Lee A. Porter; Arne Fredga

Publisher: Elsevier Science
Year: 1974
Weight: 429 KB
Volume: 3
Category: Article
ISSN: 0006-3061
DOI: 10.1016/s0006-3061(00)80037-x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Biological potency of organic selenium c

Biological potency of organic selenium compounds V. diselenides of alcohols and amines, and some selenium–containing ketones

✍ Klaus Schwarz; Arne Fredga 📂 Article 📅 1974 🏛 Elsevier Science ⚖ 347 KB

The diselenides of straight-chain aliphatie alcohols with 2 to 4 carbon atoms, and the acetic acid ester of the CJ hcmolog were similar in powney to the corresponding carboxylic acids in protecting against dietary liver necrosis in the rat. As in carboxylic acids, substitution of a methyl group at t

Biological potency of organic selenium c

Biological potency of organic selenium compounds: VI. Aliphatic seleninic acids and carboxyseleninic acids

✍ Klaus Schwarz; Arne Fredga 📂 Article 📅 1975 🏛 Elsevier Science ⚖ 493 KB

Straight-chain aliphatic seleninic acids, CH3-(CH2)n-SeOOH, with chain lengths from C4 to C17, a few dibasic acids of moderate chain length having seleninic acid groups on both ends of the molecule, HOOSe-(CH2)n-SeOOH, and a series of carbosyseleninic acids, HOOC-R-SeOOH, comprising chain lengths fr

Biological potency of organic selenium c

Biological potency of organic selenium compounds. III. Phenyl-, benzyl-, and phenylethylseleno-car☐ylic acids, and related compounds

✍ Klaus Schwarz; Arne Fredga 📂 Article 📅 1973 🏛 Elsevier Science ⚖ 703 KB

Several 2,4-dinitrophenylseleno-carboxylic acids, a number of unsubstituted and 4-substituted benzylselenocarboxylic acids, and some phenyletbylseleno-carboxylic acids have been investigated with regard to their potency in the prevention of dietary liver necrosis. The potency was strongly influenced