Incorporation of chirally deuterated putrescines into pyrrolizidine alkaloids: 
A reinvestigation

Graser, G.; Witte, L.; Robins, D. J.; Hartmann, T.

doi:10.1016/S0031-9422(98)80064-2

Item

ITEM ACTIONSEXPORT

Add to Basket

Local TagsRelease HistoryDetailsSummary

Released

Journal Article

Incorporation of chirally deuterated putrescines into pyrrolizidine alkaloids: A reinvestigation

MPS-Authors

/persons/resource/persons3895

Graser, G.
Department of Biochemistry, 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

Graser, G., Witte, L., Robins, D. J., & Hartmann, T. (1998). Incorporation of chirally deuterated putrescines into pyrrolizidine alkaloids: A reinvestigation. Phytochemistry, 47(6), 1017-1024. doi:10.1016/S0031-9422(98)80064-2.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-A634-E

Abstract

Based on previous tracer work and recent enzymatic studies it can be predicted that incorporation of (S)-1-H-2]putrescine via the symmetrical intermediate homospermidine into the necine base moiety of pyrrolizidine alkaloids (PAs) should proceed with 50