Synthesis, absolute configuration and biological activity of both enantiomers of 2-(5,6-dichloro-3-indolyl)propionic acid: New dichloroindole auxins

Bioscience, Biotechnology and Biochemistry

Volumn 65, Issue 2, 2001, Pages 270-276

  Katayama, Masato ^a   Kato, Yasuhito ^b   Marumo, Shingo ^c  

^a NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY AIST   (Japan)

^b NIPPON KAYAKU CO LTD   (Japan)

^c NAGOYA UNIVERSITY   (Japan)

Author keywords

(R) ( ) 2 (5,6 dichloro 3 indolyl)propionic acid; (S) (+) 2 (5,6 dichloro 3 indolyl)propionic acid; Avena coleoptile elongation; Dichloroindole auxin; Hypocotyl growth inhibition

Indexed keywords

2 (5,6 DICHLORO 3 INDOLYL)PROPIONIC ACID; 2-(5,6-DICHLORO-3-INDOLYL)PROPIONIC ACID; INDOLE DERIVATIVE; INDOLEACETIC ACID DERIVATIVE; PROPIONIC ACID DERIVATIVE;

ARTICLE; BRASSICA; CHEMISTRY; DRUG EFFECT; GROWTH, DEVELOPMENT AND AGING; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OAT; PLANT GROWTH; STEREOISOMERISM; SYNTHESIS;

AVENA SATIVA; BRASSICA; HYPOCOTYL; INDOLEACETIC ACIDS; INDOLES; MAGNETIC RESONANCE SPECTROSCOPY; PROPIONIC ACIDS; STEREOISOMERISM;

EID: 0035260993     PISSN: 09168451     EISSN: None     Source Type: Journal    
DOI: 10.1271/bbb.65.270     Document Type: Article

References (14)

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