✦ LIBER ✦

The use of 2,2′-dithiobis-(5-nitropyridine) as a selective reagent for the detection of thiols

✍ Scribed by D.R. Grassetti; J.F. Murray Jr.

Publisher: Elsevier Science
Year: 1969
Tongue: English
Weight: 232 KB
Volume: 41
Category: Article
ISSN: 1873-3778
DOI: 10.1016/0021-9673(64)80109-6

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Use of 2,2′-dithiobis(5-nitropyridine) f

Use of 2,2′-dithiobis(5-nitropyridine) for the heterodimerization of cysteine containing peptides. Introduction of the 5-nitro-2-pyridinesulfenyl group

✍ Francesc Rabanal; William F. DeGrado; P.Leslie Dutton 📂 Article 📅 1996 🏛 Elsevier Science 🌐 French ⚖ 308 KB

ChemInform Abstract: The Use of Diazabic

ChemInform Abstract: The Use of Diazabicyclo[2.2.2]octane as a Novel Highly Selective Dechloroacetylation Reagent.

✍ Dirk J. Lefeber; Johannis P. Kamerling; Johannes F. G. Vliegenthart 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 26 KB 👁 1 views

Vanadium 8-hydroxyquinolate as a reagent

Vanadium 8-hydroxyquinolate as a reagent for the detection of alcohols, thiols and amines

✍ A.J. Blair; D.A. Pantony 📂 Article 📅 1955 🏛 Elsevier Science 🌐 English ⚖ 679 KB

2-Trichloromethylbenzimidazole as a sele

2-Trichloromethylbenzimidazole as a selective chromogenic reagent for the detection of some azoles on thin-layer plates

✍ Leszek Konopski; Elibieta Pawłowska 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 181 KB

5-Nitrosothio-2-nitrobenzoate: A Reagent

5-Nitrosothio-2-nitrobenzoate: A Reagent for the Nitrosation of Thiol Groups in Proteins

✍ Matthew S. Studebaker; Hao Zhang; Gary E. Means 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 111 KB

Use of 2-ethoxy-1-(ethoxycarbonyl)-1, 2-

Use of 2-ethoxy-1-(ethoxycarbonyl)-1, 2-dihydroquinoline as a convenient reagent for the selective protection or derivatization of 2-hydroxycar☐ylic acids

✍ Myung Ho Hyun; Moon Hee Kang; Sang Cheol Han 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 223 KB

EEDQ has been utilized as a convenient reagent for the selective protection of the hydroxy group of 2hydroxycarboxylic acids. In the presence of an appropriate amine nucleophile, EEDQ has also been utilized as a reagent for the derivatization of both of the hydroxy and carboxylic acid group of 2-hyd