6-Substituted indanoyl isoleucine conjugates mimic the biological activity of 
coronatine

Schüler, G.; Goerls, H.; Boland, W.

doi:10.1002/1099-0690(200105)2001:9<1663::AID-EJOC1663>3.0.CO;2-I

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6-Substituted indanoyl isoleucine conjugates mimic the biological activity of coronatine

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

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Boland, W.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

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Citation

Schüler, G., Goerls, H., & Boland, W. (2001). 6-Substituted indanoyl isoleucine conjugates mimic the biological activity of coronatine. European Journal of Organic Chemistry, 2001(9), 1663-1668. doi:10.1002/1099-0690(200105)2001:9<1663:AID-EJOC1663>3.0.CO;2-I.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0012-A346-F

Abstract

The 6-substituted indanoyl isoleucine conjugates of type 12 are potent elicitors of plant secondary metabolism and tendril coiling. The 6-substituted indanoyl carboxylic acid is available in four steps from 1,2,3,4-tetrahydronaphthalene (6). Key steps p