ExLibris header image
SFX Logo
Title: l-2-amino-4-phenylbutyric acid and 2-phenylethylglucosinolate, precursors of 2-hydroxy-2-phenylethylglucosinolate
Source:

Phytochemistry [0031-9422] Underhill, E W yr:1972


Collapse list of basic services Basic
Full text
Full text available via Elsevier SD Backfile Agricultural
GO
Full text available via Elsevier SD Backfile Biochemistry
GO
Full text available via Elsevier SD Backfile Organic Chemistry
GO
Full text available via Elsevier SD Backfile Pharmacology
GO
Full text available via EZB-NALI5-00465 Elsevier Archive NL
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Oldfield, Mark F. "Biochemical characterisation of an aldoxime-forming flavoprotein involved in 2-phenylethylglucosinolate biosynthesis in Brassica species." Plant physiology and biochemistry 37.2 (1999): 99-108. Link to Full Text for this item Link to SFX for this item
2. Oldfield, M. "Synthesis of [1-13C] and [1-15N] labeled DL-homophenylalanine via a key Neber rearrangement." Journal of labelled compounds & radiopharmaceuticals 41.1 (1998): 29-36. Link to Full Text for this item Link to SFX for this item
3. Berglund, M. "SAR studies of capsazepinoid bronchodilators: The thiourea part (coupling region) and the 2-(4-chlorophenyl)ethyl moiety (C-region)." Bioorganic & medicinal chemistry 16.5 (2008): 2529-2540. Link to SFX for this item
4. Tamaoki, M. "Transcriptome analysis of O-3-exposed Arabidopsis reveals that multiple signal pathways act mutually antagonistically to induce gene expression." Plant molecular biology 53.4 (2003): 443-456. Link to Full Text for this item Link to SFX for this item
5. Varaprasad, Chamakura V. "Discovery of 3-hydroxy-4-carboxyalkylamidino-5-arylamino-isothiazoles as potent MEK1 inhibitors." Bioorganic & medicinal chemistry letters 16.15 (2006): 3975-80. Link to SFX for this item
6. Mphahlele, Malose J. "UNPRECEDENTED OUTCOME OF BASE-PROMOTED NEBER REARRANGEMENT OF O-MESYLOXIME OF 2-ARYL-1,2,3,4-TETRAHYDRO-1-METHYLSUL FONYL-4-QUINOLONE- SYNTHESIS OF 4-AMINO-2-ARYLQUINOLINES." Phosphorus, sulfur, and silicon and the related elements 166.1 (2000): 303-314. Link to SFX for this item
7. Agerbirk, N. "Sinapis phylogeny and evolution of glucosinolates and specific nitrile degrading enzymes." Phytochemistry 69.17 (2008): 2937-2949. Link to SFX for this item
8. Bennett, R. "Biosynthesis of benzylglucosinolate, cyanogenic glucosides and phenylpropanoids in Carica papaya." Phytochemistry 45.1 (1997): 59-66. Link to Full Text for this item Link to SFX for this item
9. Diez, A. "Synthetic applications of 2-aryl-4-piperidones. X. Synthesis of 3-aminopiperidines, potential substances P antagonists." Tetrahedron 51.17 (1995): 5143-5156. Link to Full Text for this item Link to SFX for this item
10. Natella, F. "Glucosinolates redox activities: Can they act as antioxidants?" Food chemistry 149 (2014): 226-232. Link to SFX for this item
11. Chelopo, M. "Anticancer activity of ruthenium(II) arene complexes bearing 1,2,3,4-tetrahydroisoquinoline amino alcohol ligands." European journal of medicinal chemistry 66 (2013): 407-414. Link to SFX for this item
12. Chierotti, M. "Solid-state NMR studies of weak interactions in supramolecular systems." Chemical communications 14 (2008): 1621-1634. Link to Full Text for this item Link to SFX for this item
13. Tabashnik, F. E. "Global variation in the genetic and biochemical basis of diamondback moth resistance to Bacillus thuringiensis." Proceedings of the National Academy of Sciences of the United States of America 94.24 (1997): 12780-12785. Link to Full Text for this item Link to SFX for this item
14. Lynch, J. "Ethylene and plant responses to nutritional stress." Physiologia plantarum 100.3 (1997): 613-619. Link to Full Text for this item Link to SFX for this item
15. Kanna, M. "Isolation of an ozone-sensitive and jasmonate-semi-insensitive Arabidopsis mutant (oji1)." Plant & cell physiology 44.12 (2003): 1301-1310. Link to SFX for this item
16. Foss, Frank W. "Synthesis and biological evaluation of γ-aminophosphonates as potent, subtype-selective sphingosine 1-phosphate receptor agonists and antagonists." Bioorganic & medicinal chemistry 15.2 (2007): 663-199. Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.