Absolute configuration of volicitin, an elicitor of plant volatile biosynthesis 
from lepidopteran larvae

Spiteller, D.; Pohnert, G.; Boland, W.

doi:10.1016/S0040-4039(00)02290-5

Item

ITEM ACTIONSEXPORT

Add to Basket

Please note that a newer version of this item is available:
https://pure.mpg.de/pubman/item/item_438679_4

DetailsSummary

Released

Journal Article

Absolute configuration of volicitin, an elicitor of plant volatile biosynthesis from lepidopteran larvae

MPS-Authors

/persons/resource/persons4189

Spiteller, D.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

/persons/resource/persons4101

Pohnert, G.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

/persons/resource/persons3812

Boland, W.
Department of Bioorganic Chemistry, 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

Spiteller, D., Pohnert, G., & Boland, W. (2001). Absolute configuration of volicitin, an elicitor of plant volatile biosynthesis from lepidopteran larvae. Tetrahedron Letters, 42(8), 1483-1485. doi:10.1016/S0040-4039(00)02290-5.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-A392-1

Abstract

The absolute configuration of the hydroxylinolenoyl moiety of volicitin (17-hydroxylinolenoyl-L-glutamine) 1a/b from four lepidopteran larvae was determined by methanolysis and derivatisation of the resulting ester with (1R)-1 -phenyl- ethylisocyanate 3