Conformational Properties of the Unnatural Amino Acid .beta.-Methylphenylalanine in a Linear Octapeptide System; Correlations of 13C-NMR Chemical Shifts with the Side-Chain Stereochemistry of These Amino Acid Residues

1994 ◽  
Vol 59 (5) ◽  
pp. 991-998 ◽  
Author(s):  
Katalin E. Kover ◽  
Ding Jiao ◽  
Sunan Fang ◽  
Victor J. Hruby
1980 ◽  
Vol 35 (7) ◽  
pp. 934-936 ◽  
Author(s):  
R. Radeglia ◽  
S. L. Spassov ◽  
R. Stefanova ◽  
S. D. Sofia

Carbon-13 chemical shifts have been measured of para-substituted 3-phenyl propanoic acid methyl esters. The substituent-induced 13C shifts of the side chain were related to Hammett substituent effects by the dual substituent parameter method. The transmission of substituent effects and the factors that influence 13C shifts are discussed


2013 ◽  
Vol 11 (1) ◽  
pp. 101-107
Author(s):  
Vidoslav Dekic ◽  
Biljana Dekic ◽  
Niko Radulovic

Synthesis and detailed spectral analysis of a new 4-substituted coumarin-amino acid derivate are presented in this paper. A new glycine derivate of (3-nitro-2-oxo-2H-chromen-4-yl)amino]acetate was prepared by condensation of 4-chloro-3-nitrocoumarin and ethyl glycinate hydrochloride. The complete assignment of 1H and 13C NMR chemical shifts of the synthesized compound was carried out by the aid of a combination of 1D (1H and 13C NMR) and 2D (1H-1H-COSY, NOESY, HSQC and HMBC) NMR experiments.


ChemInform ◽  
2010 ◽  
Vol 24 (23) ◽  
pp. no-no
Author(s):  
V. BALIAH ◽  
V. PREMASAGAR ◽  
M. UMA ◽  
A. MANGALAMUDAIYAR

Sign in / Sign up

Export Citation Format

Share Document