## Abstract The assignments of the proton NMR signals and the conformational analysis of the cystatin‐mimicking peptide K13CK (Lys‐Val‐Gly‐Gly‐Gln‐Val‐Val‐Cys‐Gly‐Ala‐Pro‐Trp‐Lys) in aqueous solution at pH 3.2 have been achieved using two‐dimensional DQF‐COSY, HOHAHA and ROESY nuclear magnetic reso
tert-Butyl 7-cycloheptatrienylperacetate: The proton NMR spectrum and conformational analysis
✍ Scribed by G. R. Jurch Jr; M. D. Johnston Jr
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 361 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The proton magnetic resonance spectrum of tert‐butyl 7‐cycloheptatrienylperacetate has been analyzed with the aid of the lanthanide shift reagents, Eu(fod)~3~ Yb(fod)~3~. Observation of the lanthanide‐induced shifts showed, in conjunction with variable temperature studies establishing the conformational purity of the cycloheptatrienyl ring, that the peracetate substituent has a definite equatorial preference.
📜 SIMILAR VOLUMES
## Abstract A theoretical and NMR‐spectroscopic conformational analysis is presented of the 3‐methyl‐1,3,5‐hexatrienes and of (__Z__)‐3‐__tert__‐butyl‐1,3,5‐hexatriene. It is shown that (__E__)‐3‐methyl‐1,3,5‐hexatriene exists mainly as the __tEt__ rotamer and (__Z__)‐3‐methyl‐1,3,5‐hexatriene as t
A conformational study of the cyclic P-casomorphin-5 analogues H-Tyr-cyclo[ -D-Om-2-Nal-Pro-Gly-J (1) (p-selective agonist; 2-Nal = 2-naphthylalanine), H-Tyr-cyclo[-D-Orn-2-Nal-D-Pro- Gly-] (2) (mixed f.~ agonistl6 antagonist) and H-Tyr-cyclo[ -D-Om-Phe-D-Pro-Gly-] (3) (highly potent p and 6 agonis
Structural and Conformational Analysis by lH NMR and 13C NMR of a New Angiotensin I Converting Enzyme Inhibitor, the tert-Butylamine Salt of (2S)-2-[ (1S)-l-Carbethoxybutylamino]-loxopropyl-(2S,3aSJaS) perhydroindole-2-carboxylic acid (Perindopril)