Titanium tetrachloride promoted conversion of carboxylic acids to carboxamides

1970 ◽  
Vol 48 (6) ◽  
pp. 983-986 ◽  
Author(s):  
James D. Wilson ◽  
Harold Weingarten

In the presence of approximately stoichiometric amounts of TiCl4, carboxylic acids and amines react at room temperature and atmospheric pressure to form carboxamides in good yields. The mono- and diformyl derivatives of 1,2-dimethylhydrazine exhibit unusual nuclear magnetic resonance spectra which are briefly discussed.

1973 ◽  
Vol 26 (7) ◽  
pp. 1487 ◽  
Author(s):  
R Colton ◽  
CJ Commons

Triphenylphosphine and triphenylarsine derivatives of W(CO)4(NO)X (X = Cl, Br, I) have been prepared. These compounds have the form mer- W(CO)3(NO)LX, cis-W(CO)2(NO)L2X, and trans-W(CO)2(NO)(PPh3)2X. A trans complex with triphenylarsine could not be prepared. Further substitution with either ligand was not achieved. In addition, the tri(ortho-, meta-, and para-)tolylphosphine and arsine complexes of W(CO)4(NO)I have been isolated. Their nuclear magnetic resonance spectra indicate interaction between neighbouring ligands in some cases, and suggest that possible rotation about the metal-phosphorus and arsenic bonds may occur in these compounds.


1976 ◽  
Vol 29 (6) ◽  
pp. 1383 ◽  
Author(s):  
AJ Canty ◽  
A Marker

Methylmercuric nitrate reacts with pyridine-2(lH)-thione (C5H5NS) in acetone to give methyl-(pyridine-2(1H)-thione)mercury(11) nitrate, [MeHg(C5H5NS)] NO3. This complex reacts with sodium bicarbonate in acetone to give methyl(pyridine-2-thiolato)mercury(11), MeHg(C5H4NS).Infrared, Raman, and nuclear magnetic resonance spectra indicate that MeHgH is bonded to sulphur in both complexes, and that protonation of nitrogen occurs on reaction of MeHg(CsH,NS) with nitric acid to give [MeHg(C5H5NS)] NO3.


1973 ◽  
Vol 51 (22) ◽  
pp. 3812-3819 ◽  
Author(s):  
D. R. Bundle ◽  
H. J. Jennings ◽  
Ian C. P. Smith

The 13C n.m.r. spectra of the 2-acetamido-2-deoxy-D-hexoses and some 3-O-acetyl and 1-phosphate derivatives are assigned and discussed. To facilitate the interpretation of the spectra, an initial assignment of the resonances in the spectrum of 2-acetamido-2-deoxy-D-glucose was required. For this purpose, both the 3-2H and 4-2H derivatives of this acetamido-hexose were synthesized. These syntheses are reported together with those of 2-acetamido-3-O-acetyl-2-deoxy-D-glucose and 2-acetamido-2-deoxy α- and β-D-glucose-1-phosphate. These model compounds were used to study substituent effects related to the 2-acetamido-2-deoxy-D-hexose-containing polysaccharide antigens of N. meningitides.


1975 ◽  
Vol 53 (18) ◽  
pp. 2748-2754 ◽  
Author(s):  
Dolatrai M. Vyas ◽  
Harold C. Jarrell ◽  
Walter A. Szarek

The carbon-13 n.m.r. spectra of derivatives of the branched-chain sugars apiose and dendroketose, and of other furanose sugars, are reported. The study has permitted assignment of the configuration at the branching carbon atom and at the anomeric center in the dendroketose derivatives.


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