𝔖 Bobbio Scriptorium
✦   LIBER   ✦

1H-1H and 13C-13C vicinal coupling constants and amino acid side chain conformation in peptides

✍ Scribed by F. Toma; M. Monnot; F. Piriou; J. Savrda; S. Fermandjian


Book ID
118314377
Publisher
Elsevier Science
Year
1980
Tongue
English
Weight
432 KB
Volume
97
Category
Article
ISSN
0006-291X

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Precise values of the 13C component vici
✍ M. C. Reddy; B. P. Nagi Reddy; K. R. Sridharan; J. Ramakrishna 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 299 KB

## Abstract From consideration of ^1^H–^1^H vicinal coupling constants and ^13^C^1^H long‐range coupling constants in a series of amino acid derivatives, the precise values of ^13^C component vicinal coupling constants have been calculated for the three minimum energy staggered rotamers for the C(

Applicability of vicinal heteronuclear (
✍ Bozhana P. Mikhova; Mario F. Simeonov; Stefan L. Spassov 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 335 KB

The vicinal "G'H, "N-'H and %-"N spin coupling constants were obtained from the 'H and =C NMR spectra of various ionic forms of the amino acids phenylalanine, a-aminobutyric acid and p-alanine, and also from their "N isotopomers. It is concluded that the "C-'H and =N-lH coupling constants are reliab

Unnaturally configured 13-epi steroids:
✍ Lee Fielding; Yolande Diepeveen; Dan Fletcher; Niall Hamilton 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 190 KB

## Abstract Six steroids with inverted stereochemistry at C‐13 (13‐__epi__) were studied. Measurement of vicinal proton–proton couplings was facilitated by a 1D TOCSY experiment, which provided efficient deconvolution of the ring D protons from other signals. A simple semi‐quantitative analysis of

Vicinal 13C13C spin–spin coupling consta
✍ James L. Marshall; Shareen A. Conn; Michael Barfield 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 376 KB

## Abstract A series of (>90% isotopic purity) ^13^C‐labeled aliphatic alcohols of the general structure CCC^13^COH were synthesized and studied by ^13^C n.m.r. to obtain all ^13^C^13^C couplings involving the labeled carbon. The ^2^__J__(CC) values were small (<0.5 Hz) and contrast with the l