Journal article
The biosynthesis of sedamine
Abstract
The biosynthesis of sedamine (IX) was studied in excised shoots of Sedum acre L. Phenyl-alanine serves as the precursor of the C 6 – C 2 side chain. The piperidine nucleus is derived from lysine, which is incorporated by way of a nonsymmetrical intermediate. These findings are consistent with Robinson's classical biogenetic hypothesis. They are incompatible with a polyacyl origin of the sedamine skeleton.
Authors
Gupta RN; Spenser ID
Journal
Canadian Journal of Chemistry, Vol. 45, No. 11, pp. 1275–1285
Publisher
Canadian Science Publishing
Publication Date
June 1, 1967
DOI
10.1139/v67-208
ISSN
0008-4042