Laser-based optical activity detection of amino acids and proteins

1987 ◽  
Author(s):  
Barbara Hollenbeck Reitsma
1987 ◽  
Vol 52 (10) ◽  
pp. 2457-2459
Author(s):  
František Jursík

Optical activity of the achiral cation [Co(NH3)6]3+ is induced both by (S)-AsnONa and (S)-GlnONa, as shown by a negative Cotton effect in the 1A1g → 1T1g transition region. An outer-sphere interaction by three-point attachment of the amides can explain the fact that substitution reaction of [Co(NH3)6]3+ with the mentioned amides in an alkaline medium is unusually slow as compared with other amino acids.


1976 ◽  
Vol 7 (8) ◽  
pp. no-no
Author(s):  
L. GIL ◽  
E. MORAGA ◽  
H. BOBADILLA ◽  
S. BUNEL ◽  
C. A. BUNTON

Fuel ◽  
1985 ◽  
Vol 64 (1) ◽  
pp. 114-118 ◽  
Author(s):  
Donald R. Bobbitt ◽  
Barbara H. Reitsma ◽  
Ann Rougvie ◽  
Edward S. Yeung ◽  
Tetsuo Aida ◽  
...  

Nature ◽  
1983 ◽  
Vol 301 (5900) ◽  
pp. 494-496 ◽  
Author(s):  
Jeffrey L. Bada ◽  
John R. Cronin ◽  
Ming-Shan Ho ◽  
Keith A. Kvenvolden ◽  
James G. Lawless ◽  
...  

1973 ◽  
Vol 51 (2) ◽  
pp. 208-214 ◽  
Author(s):  
Bernard Marinier ◽  
Yoon C. Kim ◽  
Jean-Marie Navarre

The 2,2,2-trichloroethyl esters of several N-carbobenzoxy-amino acids were prepared by reacting the corresponding acid chlorides with trichloroethanol and the carbobenzoxy groups were selectively removed by HBr–AcOH. The resulting esters were then coupled with various N-carbobenzoxy-amino acids or peptides using dicyclohexylcarbodiimide in acetonitrile to give N-carbobenzoxy-peptide trichloroethyl esters. The selective removal of the trichloroethyl protecting group was effected by reduction using zinc in acetic acid. The optical activity of the N-carbobenzoxy-peptides so obtained agreed well with the values reported in the literature. The overall results suggest that the 2,2,2-trichloroethyl group could be useful for carboxyl protection during peptide synthesis.


1962 ◽  
Vol 36 (3) ◽  
pp. 237-239
Author(s):  
Masao TANAKA ◽  
Yo KATO ◽  
Shukuo KINOSHITA
Keyword(s):  

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