This article reports a detailed reinvestigation of the reaction of bis(dialkyldithiocarbamato)zinc(II) (ZDAC) with amines. The reaction of primary amines with bis(dimethyldithiocarbamato)zinc(II) (ZDMC) results in the formation of a 1,1,3-trisubstituted thiourea, a 1,3-disubstituted thiourea, dimeth
On the Mechanism of the Reaction of o-Benzenesulfonamido-p-benzoquinone with Ammonia and Amines
✍ Scribed by Daniela Gündisch; Karl-Artur Kovar
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 452 KB
- Volume
- 327
- Category
- Article
- ISSN
- 0365-6233
No coin nor oath required. For personal study only.
✦ Synopsis
In the determination of ammonia in sera using o-benzenesulfonamido-pbenzoquinone proteins cause false positive results. These findings contradict the reaction mechanism postulated in lit., according to which a dimer is formed through an NH-bridge. As deduced by 'H-NMR-, IR-, UV-, and mass spectroscopic investigations of the reaction product and by semiempirical MO-calculations, charge transfer (CT')-complexes 3a are formed with ammonia as well as with proteins, amino acids, and amines. These CT-complexes are in a solvent dependent equilibrium with their salts 3b. Depending on the electron density of the m i n e compound, different subsequent products may be formed.
📜 SIMILAR VOLUMES
The kinetics of reaction of substituted O-benzoylbenzamidoximes with sodium methoxide in methanol were studied at 25 °C. The only reaction products are substituted benzamidoximes and methyl benzoates. The slope of the dependence of rate constant on sodium methoxide concentration gradually increases,
Crosslinked copoly(styrene-p-nitrophenylacrylates), containing 2% ( 1) or 4% DVB ( 2) were converted with various diaminoalkanes (1,2-diaminoethane 3a, 1,4diaminobutane 3b, 1,8-diaminooctane 3c) to amides. The degree of additional crosslinking depended on the chain length of the diaminoalkane, the m
The reaction of PhCH 2 C(O)NR 2 /P(O)Cl 3 (R ס alkyl) with diethyl or triethyl phosphite afforded E-vinylphosphonates 3 with high geometrical stereoselectivity and acceptable yields. The reaction with hydridophosphorane 8 gave 10, a novel trisphosphoranylphosphine oxide that can be reduced to the