Discussion 01-14

Discussion 01-14

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Unformatted text preview: d by the California Digital Library for all the UC libraries to access and use. Search for "PubMed" Available through "Catalogs and Databases" from the UCD library homepage http://www.lib.ucdavis.edu UCD enhanced version with UC Digital Library links http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?tool=cdl&holding=ucdlib&otool=cdlotool anabolic steroid abuse ---------- Related Links Referencing Papers in Writing: Example 1 Excerpt from Huntington et al.: Since the R-enantiomer binds with higher affinity and exhibits greater pharmacological effects than the corresponding Santipode, the reaction was conducted to produce only the active R-enantiomer (Chambers, 1006). References 1. Parker, Matthew A. et al. "A Novel (Benzodifuranyl)aminoalkane with Extremely Potent Activity at the 5-HT2A Receptor." Journal of Medicinal Chemistry 41 (1998): 5148-5149. 2. Monte, Aaron P. et al. "Dihydrobenzofuran Analogues of Hallucinogens. 3. Models of 4-Substituted (2,5Dimethoxyphenyl)alkylamine Derivatives with Rigidified Methoxy Groups." Journal of Medicinal Chemistry 39 (1996): 2953-2961. 3. Chambers, James J. et al. "Enantiospecific Synthesis and Pharmacological Evaluation of a Series of Super-Potent, Conformationally Restricted 5-HT2A/2C Receptor Agonists." Journal of Medicinal Chemistry 44 (2001): 1003-1010. 4. Monte, Aaron P. et al. "Dihydrobenzofuran Analogues of Hallucinogens. 4. Mescaline Derivatives." Journal of Medicinal Chemistry 40 (1997): 2997-3008. Referencing Papers in Writing: Example 2 Excerpt from Huntington et al.: Bromo-dragonFLY is a clandestine drug that as of now is not illegal, but efforts are underway to place it on the controlled substance list. This research will evaluate the most recently published method of synthesis of the drug bromo-dragonFLY, by Chambers et al. According to popular culture websites, this is the method being employed by those attempting to manufacture this drug.5,6 And since the R-enantiomer binds with higher affinity and exhibits greater pharmacological effects than the corresponding Santipode, the reaction will be conducted to produce only the active R-enantiomer. References 1. Parker, Matthew A. et al. "A Nov...
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This note was uploaded on 07/22/2009 for the course ETX 001 taught by Professor Matthewwood during the Winter '09 term at UC Davis.

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