In:
Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 14, No. 12 ( 1959-12-1), p. 802-809
Abstract:
With the aid of DL-phenylalanine- [carboxyl- 14 C] it has been demonstrated that the carbon skeleton of phenylalanine is incorporated into 7-hydroxy-4-methoxy-iso-flavone (formononetin) in red clover and that a rearrangement takes place. The isotope distribution found can be explained by a migration of either a phenyl or a benzoyl group in the course of the biogenesis. A biogenetic scheme is presented which explains the formation of all flavones, iso-flavones and coumestrol found in red clover.
Type of Medium:
Online Resource
ISSN:
1865-7117
,
0932-0776
DOI:
10.1515/znb-1959-1209
Language:
English
Publisher:
Walter de Gruyter GmbH
Publication Date:
1959
detail.hit.zdb_id:
2078109-X
detail.hit.zdb_id:
124635-5
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