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Synthesis of the Four Stereoisomers of 6-Acetoxy-19-methylnonacosane, the Most Potent Component of the Female Sex Pheromone of the New World Screwworm Fly, with Special Emphasis on Partial Racemization in the Course of Catalytic Hydrogenation.
- Published in:
- European Journal of Organic Chemistry, 2004, v. 2004, n. 5, p. 1089, doi. 10.1002/ejoc.200300669
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Chiral discrimination of primary amines by HPLC after labeling with a chiral derivatization reagent, trans-2-(2,3-anthracenedicarboximido)-cyclohexanecarbonyl chloride.
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- Journal of Separation Science, 2006, v. 29, n. 10, p. 1390
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- Article
Chiral discrimination of secondary alcohols by both <sup>1</sup>H-NMR and HPLC after labeling with a chiral derivatization reagent, 2-(2,3-anthracenedicarboximide)cyclohexane carboxylic acid.
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- Chirality, 2005, v. 17, n. S1, p. S171, doi. 10.1002/chir.20141
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- Article
Crystalline Structure of N-(S)-2-Heptyl (1R ,2R)-2-(2,3-Anthracenedicarboximido)cyclohexanecarboxamide That Differs from Its Preferred Conformation in the Solvent Used for Crystallization.
- Published in:
- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 10, p. 2002, doi. 10.1271/bbb.69.2002
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- Article
Synthesis of the Four Stereoisomers of 7-Acetoxy-15-methylnonaeosane, a Component of the Female Sex Pheromone of the Screwworm Fly, Cochlzomyia hominworax.
- Published in:
- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 8, p. 1768, doi. 10.1271/bbb.68.1768
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- Article