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

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.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-A346-F Version Permalink: https://hdl.handle.net/21.11116/0000-0009-384D-3
Genre: Journal Article

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BOL123.pdf (Publisher version), 0B
 
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 Creators:
Schüler, G.1, Author           
Goerls, H., Author
Boland, W.1, Author           
Affiliations:
1Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society, ou_24028              

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Free keywords: acylation; coronatine; amino acids; bioorganic chemistry; metabolism Pseudomonas-syringae pathovars; jasmonic acid; (+/-)- coronafacic acid; volatile biosynthesis; acyclic homoterpenes; phaseolus-lunatus; tendril-coiling; higher-plants; induction; phytotoxin
 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

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 Dates: 2001
 Publication Status: Issued
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 Rev. Type: -
 Identifiers: Other: BOL123
DOI: 10.1002/1099-0690(200105)2001:9<1663::AID-EJOC1663>3.0.CO;2-I
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Title: European Journal of Organic Chemistry
  Other : Eur. J. Org. Chem.
Source Genre: Journal
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Publ. Info: Weinheim, Germany : Wiley-VCH
Pages: - Volume / Issue: 2001 (9) Sequence Number: - Start / End Page: 1663 - 1668 Identifier: ISSN: 1434-193X
CoNE: https://pure.mpg.de/cone/journals/resource/954926953810