Determination of the structure of fusaproliferin by1H-NMR and distance geometry
✍ Scribed by Cesare Manetti; Vincenzo Fogliano; Alberto Ritieni; Antonello Santini; Giacomino Randazzo; Antonio Logrieco; Luisa Mannina; Anna Laura Segre
- Publisher
- Springer
- Year
- 1995
- Tongue
- English
- Weight
- 457 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1040-0400
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Utilizing 2D NMR spectroscopy (COSY, NOESY, TOCSY, inverse detected ^1^H/^13^C correlation spectroscopy), the ^1^H and ^13^C NMR spectra of the ketone and epoxide precursors of β‐chamigrene were assigned. The dihedral angles and distances determined from NMR measurements provide input p
## Abstract The three‐dimensional structure of a cyclic bouvardin analogue, cyclo (‐Pro‐MeTyr‐Ala‐MeTyr‐MeTyr‐D‐Ala‐) has been determined by distance geomtry calculation and restrained energy minimization from nmr data. The preparation of the input for the distance geometry calculations, the modifi
## Abstract The thermodynamic products (ε‐lactams) of the degradation of ten different spirocyclic oxaziridines were analyzed by ^1^H and ^13^C NMR spectroscopy. The preferred conformations were determined by examining the homonuclear spin–spin coupling constant and the chemical shift effects of th
To identify the peptide conformation that is preferentially secondary structural elements. The analysis of the average properties of these compounds indicate the presence of some recognized by the receptor, we have synthetized by solidphase method a series of deltorphin I analogs with increasing dis