6-Cyclopropylpurines as Novel Potent Analogs of Cytokinins
Author:
Publisher
Springer Science and Business Media LLC
Subject
Plant Science,Agronomy and Crop Science
Link
http://link.springer.com/content/pdf/10.1007/s00344-004-0057-8.pdf
Reference19 articles.
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2. Bråthe A, Andresen G, Gundersen LL, Malterud KE, Rise F. 2002. Antioxidant activity of synthetic cytokinin analogs: 6-Alkenyl and 6-alkynylpurines as novel 15-lipoxygenase inhibitors. Bioorg Med Chem 10:1581–1586
3. Bråthe A, Gundersen LL, Nissen-Meyer J, Rise F, Spilsberg B. 2003, Cytotoxic activity of 6-alkynyl-and 6-alkenylpurines. Bioorg Med Chem Lett 13:877–880
4. Bugg CE, Thewalt U. 1972. Crystal structure of N6-(Δ2-isopentenyl)adenine, a base in the anticodon loop of some tRNAs. Biochem Biophys Res Commun 46:779–784
5. Galuszka P. Frébort I. Sebela M. Sauer P. Jacobsen S. 2001. Cytokinin oxidase or dehydrogenase? Mechanism of cytokinin degradation in cereals. Eur J Biochem 268:450–461
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1. Synthesis of (E)-6-alkenylpurines via Pd-catalyzed stannation/protodestannation tandem process of alkynylpurines;Collection of Czechoslovak Chemical Communications;2010
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3. Cyclization and rearrangement products from coupling reactions between terminal o-alkynylphenols or o-ethynyl(hydroxymethyl)benzene and 6-halopurines;Tetrahedron;2006-06
4. Synthesis of Optically Active 6-Alkynyl- and 6-Alkylpurines as Cytokinin Analogs and Inhibitors of 15-Lipoxygenase; Studies of Intramolecular Cyclization of 6-(Hydroxyalkyn-1-yl)purines;European Journal of Organic Chemistry;2005-12
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