Metabolic inversion of the 3-hydroxy function of brassinosteroids

Kolbe, A.; Schneider, B.; Porzel, A.; Adam, G.

doi:10.1016/S0031-9422(98)00037-5

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Journal Article

Metabolic inversion of the 3-hydroxy function of brassinosteroids

MPS-Authors

/persons/resource/persons4159

Schneider, B.
Research Group Biosynthesis / NMR, MPI for Chemical Ecology, Max Planck Society;

External Resource

No external resources are shared

Fulltext (restricted access)

There are currently no full texts shared for your IP range.

Fulltext (public)

There are no public fulltexts stored in PuRe

Supplementary Material (public)

There is no public supplementary material available

Citation

Kolbe, A., Schneider, B., Porzel, A., & Adam, G. (1998). Metabolic inversion of the 3-hydroxy function of brassinosteroids. Phytochemistry, 48(3), 467-470. doi:10.1016/S0031-9422(98)00037-5.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-B500-D

Abstract

Exogenously applied 3-dehydro-24-epi-teasterone is transformed by cell suspension cultures of Lycoperaicon esculentum to give the metabolites 24-epi-teasterone and 24-epi-typhasterol in about equal but low quantities. The major portion of 24-epi-teaster