Racemization (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Racemization" in English language version.

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7nih.gov

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6doi.org

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1libretexts.org

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1ualberta.ca

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1semanticscholar.org

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1nytimes.com

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1books.google.com

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archive.org

Streitwieser A, Heathcock CH (1985). Introduction to Organic Chemistry (3rd ed.). Maxwell MacMillan. ISBN 978-0-02-946720-6.

books.google.com

Reist M, Testa B, Carrupt PA (2003). "Drug Racemization and Its Significance in Pharmaceutical Research". In Eichelbaum MF, Testa B, Somogyi A (eds.). Stereochemical Aspects of Drug Action and Disposition. Handbook of Experimental Pharmacology. Vol. 153. pp. 91–112. doi:10.1007/978-3-642-55842-9_4. ISBN 978-3-642-62575-6.

doi.org

Brooks WH, Guida WC, Daniel KG (2011). "The significance of chirality in drug design and development". Current Topics in Medicinal Chemistry. 11 (7): 760–770. doi:10.2174/156802611795165098. PMC 5765859. PMID 21291399.
Arnold LE, Wender PH, McCloskey K, Snyder SH (December 1972). "Levoamphetamine and dextroamphetamine: comparative efficacy in the hyperkinetic syndrome. Assessment by target symptoms". Archives of General Psychiatry. 27 (6): 816–822. doi:10.1001/archpsyc.1972.01750300078015. PMID 4564954.
Teo SK, Colburn WA, Tracewell WG, Kook KA, Stirling DI, Jaworsky MS, et al. (2004). "Clinical pharmacokinetics of thalidomide". Clinical Pharmacokinetics. 43 (5): 311–327. doi:10.2165/00003088-200443050-00004. PMID 15080764. S2CID 37728304.
Moehler TM, Hillengass J, Glasmacher A, Goldschmidt H (December 2006). "Thalidomide in multiple myeloma". Current Pharmaceutical Biotechnology. 7 (6): 431–440. doi:10.2174/138920106779116919. PMID 17168659.
Jacquot C, David DJ, Gardier AM, Sánchez C (2007). "[Escitalopram and citalopram: the unexpected role of the R-enantiomer]". L'Encephale. 33 (2): 179–187. doi:10.1016/s0013-7006(07)91548-1. PMID 17675913.
Reist M, Testa B, Carrupt PA (2003). "Drug Racemization and Its Significance in Pharmaceutical Research". In Eichelbaum MF, Testa B, Somogyi A (eds.). Stereochemical Aspects of Drug Action and Disposition. Handbook of Experimental Pharmacology. Vol. 153. pp. 91–112. doi:10.1007/978-3-642-55842-9_4. ISBN 978-3-642-62575-6.

libretexts.org

chem.libretexts.org

Kennepohl D, Farmer S (2019-02-13). "6.7: Optical Activity and Racemic Mixtures". Chemistry LibreTexts. Retrieved 2022-11-16.

nih.gov

pubmed.ncbi.nlm.nih.gov

Brooks WH, Guida WC, Daniel KG (2011). "The significance of chirality in drug design and development". Current Topics in Medicinal Chemistry. 11 (7): 760–770. doi:10.2174/156802611795165098. PMC 5765859. PMID 21291399.
Mitchell AG (1998). "Racemic drugs: racemic mixture, racemic compound, or pseudoracemate?" (PDF). Journal of Pharmacy & Pharmaceutical Sciences. 1 (1): 8–12. PMID 10942967.
Arnold LE, Wender PH, McCloskey K, Snyder SH (December 1972). "Levoamphetamine and dextroamphetamine: comparative efficacy in the hyperkinetic syndrome. Assessment by target symptoms". Archives of General Psychiatry. 27 (6): 816–822. doi:10.1001/archpsyc.1972.01750300078015. PMID 4564954.
Teo SK, Colburn WA, Tracewell WG, Kook KA, Stirling DI, Jaworsky MS, et al. (2004). "Clinical pharmacokinetics of thalidomide". Clinical Pharmacokinetics. 43 (5): 311–327. doi:10.2165/00003088-200443050-00004. PMID 15080764. S2CID 37728304.
Moehler TM, Hillengass J, Glasmacher A, Goldschmidt H (December 2006). "Thalidomide in multiple myeloma". Current Pharmaceutical Biotechnology. 7 (6): 431–440. doi:10.2174/138920106779116919. PMID 17168659.
Jacquot C, David DJ, Gardier AM, Sánchez C (2007). "[Escitalopram and citalopram: the unexpected role of the R-enantiomer]". L'Encephale. 33 (2): 179–187. doi:10.1016/s0013-7006(07)91548-1. PMID 17675913.

ncbi.nlm.nih.gov

Brooks WH, Guida WC, Daniel KG (2011). "The significance of chirality in drug design and development". Current Topics in Medicinal Chemistry. 11 (7): 760–770. doi:10.2174/156802611795165098. PMC 5765859. PMID 21291399.

nytimes.com

Stolberg SG (17 July 1998). "Thalidomide Approved to Treat Leprosy, With Other Uses Seen". The New York Times. Retrieved 8 January 2012.

semanticscholar.org

api.semanticscholar.org

Teo SK, Colburn WA, Tracewell WG, Kook KA, Stirling DI, Jaworsky MS, et al. (2004). "Clinical pharmacokinetics of thalidomide". Clinical Pharmacokinetics. 43 (5): 311–327. doi:10.2165/00003088-200443050-00004. PMID 15080764. S2CID 37728304.

ualberta.ca

sites.ualberta.ca

Mitchell AG (1998). "Racemic drugs: racemic mixture, racemic compound, or pseudoracemate?" (PDF). Journal of Pharmacy & Pharmaceutical Sciences. 1 (1): 8–12. PMID 10942967.

web.archive.org

"Use of thalidomide in leprosy". WHO:leprosy elimination. World Health Organization. Archived from the original on November 10, 2006. Retrieved 22 April 2010.

who.int

"Use of thalidomide in leprosy". WHO:leprosy elimination. World Health Organization. Archived from the original on November 10, 2006. Retrieved 22 April 2010.