Use of carboxylic acids as chiral solvating agents for the determination of optical purity of chiral amines by NMR spectroscopy

1988 ◽  
Vol 53 (22) ◽  
pp. 5335-5341 ◽  
Author(s):  
Scott C. Benson ◽  
Ping Cai ◽  
Marcelo Colon ◽  
Mohammed A. Haiza ◽  
Maritherese Tokles ◽  
...  
ChemInform ◽  
1989 ◽  
Vol 20 (18) ◽  
Author(s):  
S. C. BENSON ◽  
P. CAI ◽  
M. COLON ◽  
M. A. HAIZA ◽  
M. TOKLES ◽  
...  

2006 ◽  
Vol 71 (3) ◽  
pp. 1119-1130 ◽  
Author(s):  
Rosa García ◽  
José M. Seco ◽  
Saulo A. Vázquez ◽  
Emilio Quiñoá ◽  
Ricardo Riguera

1986 ◽  
Vol 40 (3) ◽  
pp. 348-351 ◽  
Author(s):  
David E. Schiff ◽  
John G. Verkade ◽  
Robert M. Metzler ◽  
Thomas G. Squires ◽  
Clifford G. Venier

Derivatization of compounds containing -OH groups can be accomplished quantitatively with 1,3,2-dioxaphospholanyl chloride. The chemical shifts of phosphorus in the derivatives clearly differentiate alcohols from phenols and carboxylic acids. Quantitation is obtained by use of 31P FT-NMR spectroscopy in the presence of 2,2,6,6-tetrameth-ylpiperidinyloxy free radical to shorten relaxation times. Compounds with phosphorus chemical shifts differing by as little as 0.1 ppm can be separately determined.


2019 ◽  
Vol 17 (6) ◽  
pp. 1466-1470 ◽  
Author(s):  
Liwen Bai ◽  
Pian Chen ◽  
Jiangxia Xiang ◽  
Jiarui Sun ◽  
Xinxiang Lei

We extended actinomycin D as a practical CSA for rapid enantiomeric determination of chiral carboxylic acids by1H NMR spectroscopy.


1973 ◽  
Vol 5 (9) ◽  
pp. 413-417 ◽  
Author(s):  
Günther Snatzke ◽  
John E. Fox ◽  
Mustafa M. El-Abadelah

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