Chiral metal complexes. 14. High resolution 1H NMR studies of β-[Co(2,5-diaza-3-methyl-1,6-di(2-pyridyl)hexane)(alaninate)]2+ and related 1,2-diaminoethane complexes

1984 ◽  
Vol 88 (2) ◽  
pp. 193-199 ◽  
Author(s):  
Jill A. Chambers ◽  
Terence J. Goodwin ◽  
Moh'D W. Mulqi ◽  
Peter A. Williams ◽  
Robert S. Vagg
Biochemistry ◽  
1983 ◽  
Vol 22 (20) ◽  
pp. 4842-4845 ◽  
Author(s):  
Takashi Iwashita ◽  
Yoshiki Mino ◽  
Hideo Naoki ◽  
Yukio Sugiura ◽  
Kyosuke Nomoto

2003 ◽  
Vol 42 (26) ◽  
pp. 8811-8817 ◽  
Author(s):  
Pratip K. Bhattacharya ◽  
Holly J. Lawson ◽  
Jacqueline K. Barton

1980 ◽  
Vol 622 (2) ◽  
pp. 219-230 ◽  
Author(s):  
Jürgen Lauterwein ◽  
Larry R. Brown ◽  
Kurt Wüthrich

1990 ◽  
Vol 55 (4) ◽  
pp. 1106-1111 ◽  
Author(s):  
John Matsoukas ◽  
Paul Cordopatis ◽  
Raghav Yamdagni ◽  
Graham J. Moore

The conformational properties of the Sarmesin analogues [N-MeAib1, Tyr(Me)4]ANGII and [N-MeAib1, Tyr(Me)4, Ile8]ANGII in hexadeutero-dimethysulfoxide were investigated by Nuclear Overhauser Effect (NOE) Enhancement Studies. Cis-trans isomers (ratio 1 : 6) due to restricted rotation of the His-Pro bond were observed. Interresidue interactions between the His Cα proton and the two Pro Cδ protons revealed that the major isomer was the trans.


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