## Abstract Based on readily available chloralamides, a preparative method for the synthesis of hitherto unknown 2,5βdiarylβ3a,6aβdihydro[1,3]thiazolo[4,5β__d__][1,3]thiazoles with the Lawesson reagent has been elaborated. Β© 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:677β681, 2008; Published o
Removal of sulfhydryl groups with 1,3,4,6-tetrachloro-3a, 6a-diphenylglycoluril: Application to the assay of protein in the presence of thiol reagents
β Scribed by Ronald W. McClard
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- English
- Weight
- 280 KB
- Volume
- 112
- Category
- Article
- ISSN
- 0003-2697
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β¦ Synopsis
The chloroamide compound 1,3,4,6-tetrachloro-3a, 6a-diphenylglycoluril is a useful solid-phase reagent for the oxidative removal of sulfhydryl groups from solution. The reaction with dithiothreitol is rapid and first order (/robs = 0.3 min-I). Titration of dithiothreitol with chloroglycoluril shows that one suIfhydry1 group reacts per chloroamide group. Chloroglycoluril can be conveniently employed as a solid-phase reagent to remove suhhydryl groups prior to assay for protein using the standard method of 0. H. Lowry,
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## Abstract The synthesis of Ξ·^6^β(4aβmethylβ1,2,3,4βtetrahydroβ4a__H__βcarbazole)tricarbonylchromium (**3**) is described, and its reactivity with organolithium reagents have been analysed. The addition of RLi (R= H, Me, __n__βBu, __tert__βBu) to **3** affords the corresponding __endo/exo__ tricar
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