| Literature DB >> 23604939 |
K H Ling1, B J Chen, Y W Peng, S C Tsai, F C Peng, C K Yang.
Abstract
The chemical reaction of cleavaging territrem B to give 3,4,5-trimethoxy benzoic acid by alkaline hydrogen peroxide was investigated. The method was applied for confirmation of the chemical structure of the aromatic moiety of territrem A, A', B, and B'. The physicochemical properties of the aromatic cleavage product of territrem Aindicated the structure as 3,4-methylendioxy, 5-methoxy benzoic acid (or 4-methoxy, 6-carboxy, 1, 3-benzodioxole). The experiment also gave the evidences that territrem A and A', on the other hand territrem B and B' have the identical aromatic moieties on their structures.Entities:
Year: 1987 PMID: 23604939 DOI: 10.1007/BF03191990
Source DB: PubMed Journal: Mycotoxin Res ISSN: 0178-7888 Impact factor: 3.833