Synthesis and potato cell expansion-inducing activity of the stereochemically restricted bicyclic analogue of 7-epi-jasmonic Acid

Bioscience, Biotechnology and Biochemistry

Volumn 64, Issue 12, 2000, Pages 2702-2705

  Toshima, Hiroaki ^a   Nara, Shinji ^a   Fujino, Yumiko ^a   Ichihara, Akitami ^a  

^a HOKKAIDO UNIVERSITY   (Japan)

Author keywords

7 epi jasmonic acid; Bicyclo 3.3.0 octane; Jas monic acid analogue; Phytohormone

Indexed keywords

BICYCLO COMPOUND; CYCLOPENTANE DERIVATIVE; JASMONIC ACID;

ARTICLE; BIOCHEMISTRY; CHEMISTRY; CYTOLOGY; DRUG EFFECT; DRUG SCREENING; METHODOLOGY; POTATO; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

BICYCLO COMPOUNDS; BIOCHEMISTRY; CYCLOPENTANES; DRUG EVALUATION, PRECLINICAL; SOLANUM TUBEROSUM; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0034568127     PISSN: 09168451     EISSN: 13476947     Source Type: Journal    
DOI: 10.1271/bbb.64.2702     Document Type: Article

References (12)

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8. Compound 6 was obtained as an inseparable mixture of diastereomers because racemic 2,3-butandiol containingca.5% of the meso form was used for acetali-zation.
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12. A mixture of minor (±)-l (5%) and major(±)-2(95%), which had been prepared from commercially available methyl (±)-jasmonate, was used as the JA standard for the bioassay.