Biosynthesis of phenolic tetrahydroisoquinoline alkaloids of peyote

Autor:	H. Rosenberg, M. Takido, A.G. Paul, K. L. Khanna
Rok vydání:	1970
Předmět:	Stereochemistry Tetrahydroisoquinoline Pellotine Anhalidine Plant Science General Medicine Methylation Anhalamine Horticulture Biology Biochemistry Hydroxylation chemistry.chemical_compound Biosynthesis chemistry Dopamine medicine Organic chemistry Molecular Biology medicine.drug
Zdroj:	Phytochemistry. 9:1811-1815
ISSN:	0031-9422
DOI:	10.1016/s0031-9422(00)85597-1
Popis:	Data are presented supporting a proposed pathway of biosynthesis of the phenolic tetrahydroisoquinoline alkaloids of peyote from dopamine. It is suggested that meta - O -methylation of dopamine, hydroxylation in the 5-position, para - O -methylation and finally cyclizations yield anhalamine, anhalidine, anhalonidine and pellotine.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f8c968292e5ff8acd8e403beda23c5c8 https://doi.org/10.1016/s0031-9422(00)85597-1 Zobrazit plný text záznamu