Synthesis, absolute configuration and biological activities of both enantiomers of 2-(5,7-dichloro-3-indolyl)propionic acid: A novel dichloroindole auxin and antiauxin

Bioscience, Biotechnology and Biochemistry

Volumn 68, Issue 6, 2004, Pages 1287-1292

  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 (5,7 dichloro 3 indolyl)propionic acid; (S) (+) 2 (5,7 dichloro 3 indolyl)propionic acid; Antiauxin; Auxin; Avena coleoptile elongation

Indexed keywords

INDOLE DERIVATIVE; INDOLEACETIC ACID DERIVATIVE;

ARTICLE; CHEMISTRY; CONFORMATION; COTYLEDON; DRUG EFFECT; OAT; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION; SYNTHESIS;

AVENA SATIVA; COTYLEDON; INDOLEACETIC ACIDS; INDOLES; MOLECULAR CONFORMATION; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP;

AVENA; AVENA SATIVA;

EID: 4544233004     PISSN: 09168451     EISSN: None     Source Type: Journal    
DOI: 10.1271/bbb.68.1287     Document Type: Article

References (18)

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