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Bioscience, Biotechnology, and Biochemistry Volume 64, 2000 - Issue 4
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Original Articles

Synthesis and Biological Activities of 4-Chloroindole-3-acetic Acid and Its Esters

Masato KATAYAMALaboratory of Bioorganic Chemistry, Department of Chemistry, National Industrial Research Institute of Nagoya
Pages 808-815 | Received 18 Nov 1999, Accepted 15 Dec 1999, Published online: 22 May 2014

Citations (19)

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Masato KATAYAMA, Yasuhito KATO & Shingo MARUMO. (2004) 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 68:6, pages 1287-1292.
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Articles from other publishers (18)

Koji Yamada, Mariko Ohta, Go Kitamura, Suzuka Tsutsumiguchi & Takahide Nishi. (2023) Facile synthesis of indole 3-acetic acid and azaindole 3-acetic acid derivatives. Tetrahedron 135, pages 133328.
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Björn C. G. Söderberg & William F. Berkowitz. 2004. Organic Reactions. Organic Reactions 417 640 .
Mussa Quareshy, Justyna Prusinska, Martin KiefferKosuke Fukui, Alonso J. Pardal, Silke LehmannPatrick SchaferCharo I. del Genio, Stefan KepinskiKenichiro Hayashi, Andrew Marsh & Richard M. Napier. (2018) The Tetrazole Analogue of the Auxin Indole-3-acetic Acid Binds Preferentially to TIR1 and Not AFB5. ACS Chemical Biology 13:9, pages 2585-2594.
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Wei TangWei TangYongjun Fei. (2018) Using A “Superrooting”Cultivar of Taxus Chinensis Var. Mairei to Unravel Antioxidative Enzymes’ and Micrornas’ Role on Adventitious Rooting. Journal of Enzymes 1:2, pages 1-18.
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Ranjith Kumavath. 2015. Antimicrobials. Antimicrobials 143 154 .
Yasushi Shimizu-Mitao & Tatsuo Kakimoto. (2014) Auxin Sensitivities of All Arabidopsis Aux/IAAs for Degradation in the Presence of Every TIR1/AFB. Plant and Cell Physiology 55:8, pages 1450-1459.
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Ganesh N. Naik, Raghavendra P. Bakale, Aishakhanam H. Pathan, Shashikala G. Ligade, Shreenivas A. Desai & Kalagouda B. Gudasi. (2013) 2,4-Dichlorophenoxyacetic Acid Derived Schiff Base and Its Lanthanide(III) Complexes: Synthesis, Characterization, Spectroscopic Studies, and Plant Growth Activity. Journal of Chemistry 2013, pages 1-13.
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Kaori Yoshimoto, Yoshiteru Noutoshi, Ken-ichiro Hayashi, Ken Shirasu, Taku Takahashi & Hiroyasu Motose. (2012) A Chemical Biology Approach Reveals an Opposite Action between Thermospermine and Auxin in Xylem Development in Arabidopsis thaliana. Plant and Cell Physiology 53:4, pages 635-645.
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Chikako Honda, Shinnosuke Kusaba, Takaaki Nishijima & Takaya Moriguchi. (2011) Transformation of kiwifruit using the ipt gene alters tree architecture. Plant Cell, Tissue and Organ Culture (PCTOC) 107:1, pages 45-53.
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Masato Katayama, Takao Saito & Kozo Kanayama. (2010) 5,6-Dichloroindole-3-acetic acid and 4-chloroindole-3-acetic acid, two potent candidates for new rooting promoters without estrogenic activity. Journal of Pesticide Science 35:2, pages 134-137.
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Darleen A. DeMason & Patricia L. Polowick. (2009) Patterns of DR5::GUS Expression in Organs of Pea ( Pisum sativum ) . International Journal of Plant Sciences 170:1, pages 1-11.
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Tomáš Řezanka, Lumír O. Hanuš, Valery M. Dembitsky & Karel Sigler. (2008) Identification of the Eight-Membered Heterocycles Hicksoanes A–C from the GorgonianSubergorgia hicksoni. European Journal of Organic Chemistry 2008:7, pages 1265-1270.
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N. Kumavath Ranjith, Ch. Sasikala & Ch. Venkata Ramana. (2007) Rhodethrin: a novel indole terpenoid ether produced by Rhodobacter sphaeroides has cytotoxic and phytohormonal activities. Biotechnology Letters 29:9, pages 1399-1402.
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Eiji Kageyama, Masato Katayama, Yuko Masui, Koji Kageyama & Youichi Kawabata. (2006) Synthesis and plant growth-regulating activities of L-lactic acid derivatives of 4-chloroindole-3-acetic acid. Journal of Pesticide Science 31:2, pages 130-138.
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M.R. Sunayana, Ch. Sasikala & Ch.V. Ramana. (2005) Rhodestrin: A Novel Indole Terpenoid Phytohormone from Rhodobacter sphaeroides. Biotechnology Letters 27:23-24, pages 1897-1900.
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M. R. Sunayana, Ch. Sasikala & Ch. V. Ramana. (2005) Production of a novel indole ester from 2-aminobenzoate by Rhodobacter sphaeroides OU5. Journal of Industrial Microbiology & Biotechnology 32:2, pages 41-45.
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Rekha Chawla & Darleen A. DeMason. (2004) Molecular expression of PsPIN1, a putative auxin efflux carrier gene from pea (Pisum sativum L.). Plant Growth Regulation 44:1, pages 1-14.
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Jason Siu, Ian R. Baxendale & Steven V. Ley. (2004) Microwave assisted Leimgruber–Batcho reaction for the preparation of indoles, azaindoles and pyrroylquinolines. Org. Biomol. Chem. 2:2, pages 160-167.
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