𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The 13C NMR spectrum of 5- O-β-D-primeverosyl genkwanine

✍ Scribed by A. García-Granados; J. M. Sáenz de Buruaga


Publisher
John Wiley and Sons
Year
1980
Tongue
English
Weight
158 KB
Volume
13
Category
Article
ISSN
0749-1581

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The ^13^C NMR spectra of 5‐O‐β‐D‐primeverosyl genkwanine and its acetate are studied and assignments are proposed.


📜 SIMILAR VOLUMES


Complete 1H and 13C NMR assignments of s
✍ Shaheen Faizi; Muhammad Ali; Rubeena Saleem; Irfanullah; Sarah Bibi 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 121 KB

## Abstract Unambiguous and complete assignments of ^1^H and ^13^C NMR chemical shifts for stigma‐5‐en‐3‐__O__‐β‐glucoside, isolated from __Brassica rapa__ sb.sp. __campestris__ and __Aloe barbadensis__, and its acetyl derivative are presented, based on DEPT, HETCOR, COLOC, HMBC, COSY‐45°, NOESY an

The Infrared Spectrum of 13C2D2: The Ben
✍ E. Canè; G. Cazzoli; G.Di Lonardo; L. Dore; R. Escribano; L. Fusina 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 169 KB

The vibration-rotation spectrum of 13 C 2 D 2 has been recorded in the infrared region between 420 and 1100 cm -1 with an effective resolution ranging from 0.004 to 0.006 cm -1 , and in the millimeter-wave region between 68 and 518 GHz. A total of about 1400 rovibrational transitions (66 of which ha

Configurational assignment by 13C NMR of
✍ J. P. Bégué; D. Bonnet-Delpon 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 258 KB

## Abstract The configurational assignment of stereoisomeric 3‐bromo‐3‐acyl derivatives of steroids in both the 5α and 5β series has been carried out by comparing the ^13^C chemical shifts of C‐3. A downfield shift is observed for C‐3, bearing a bromine and an acyl group, on going from the isomer w

Assignment of the relative configuration
✍ Jorge Antonio Guerrero-Alvarez; Antonio Moncayo-Bautista; Armando Ariza-Castolo 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 171 KB

## Abstract The relative configuration of 11 1,4‐diazaspiro[4.5]decanes (**1a–1j** and **1m**), 15 1,4‐oxazaspiro[4.5]decanes (**2a–2o**) and 10 1,4‐dioxaspiro[4.5]decanes (**3a–3n**) substituted at the 2‐, 6‐, 7‐ or 8‐position by a methyl group or using the __tert__‐butyl group as a model for the