## Abstract An NMR study of a new stereoisomer of isoreserpiline pseudoindoxyl alkaloid is described. The complete ^1^H and ^13^C NMR assignments of the compound were carried out using COSY, HMQC and HMBC. Stereochemistry at carbons C‐2, C‐3, C‐15, C‐20 and C‐19 was established using values of ^1^H
1H-nmr studies on the structure of a new thionin from barley endosperm
✍ Scribed by M Bruix; C González; J Santoro; F Soriano; A Rocher; E Méndez; M Rico
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1995
- Tongue
- English
- Weight
- 930 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0006-3525
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