Assignment of13C-NMR Spectra of Grayanotoxin-I and -III
- 1 March 1979
- journal article
- research article
- Published by Oxford University Press (OUP) in Agricultural and Biological Chemistry
- Vol. 43 (3) , 631-635
- https://doi.org/10.1080/00021369.1979.10863476
Abstract
As the first step towards the biosynthetic studies on grayanotoxins with the aid of 13C isotope, the 13C-NMR spectra of grayanotoxin-I and -III were assigned. Unambiguous assignments were achieved except for the C–9 and C–13 resonances in G-I by selective proton decoupling technique as well as by comparison with chemical shift values of the related compounds.This publication has 2 references indexed in Scilit:
- Stereostructure of α-Dihydrograyanotoxin-IIAgricultural and Biological Chemistry, 1978
- Transformation of 6β-Bromo-4,4-dimethyl-1α,2α-epoxy-3α,5α-oxidocholestane into 6β-Bromo-4,4-dimethy1-3α,5α-oxido-5(10→1βH)abeo-10(19)-cholesten-2α-olAgricultural and Biological Chemistry, 1977