## Abstract The ^1^H and ^13^C spectra of bicyclo[3.1.0]hexanes and thujanes have been recorded and assigned. Application of the Karplus equation has yielded dihedral angles, and a computer calculation of the angle of ring buckle as a function of the main dihedral angles has been carried out. The c
Refinement of the solution structure of bicyclo[3.1.0]-hexan-3-one by 1H- and 13C-lanthanide induced shift (L.I.S.) analysis
β Scribed by Raymond J. Abraham; Derek J. Chadwick; Fernando Sancassan
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 181 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Although lanthanide shift reagents have rightly become a routine tool in n.m.r. spectroscopy, the decline in the number of publications dealing with their detailed structural application perhaps reflects a growing disenchantment with their utility arising from the assumptions implied in their use. Surprisingly, after the early work of R. J. P. Williams and co-workers on the determination of the conformations of AMP and TMP in aqueous solution' , there has been little effort expended in attempts to ' 0.
π SIMILAR VOLUMES
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)