Chirality (chemistry) (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Chirality (chemistry)" in English language version.

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23doi.org

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9nih.gov

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6iupac.org

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5semanticscholar.org

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2harvard.edu

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1worldcat.org

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1newscientist.com

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1web.archive.org

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1uottawa.ca

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1jstor.org

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books.google.com

Eliel, Ernest Ludwig; Wilen, Samuel H.; Mander, Lewis N. (1994). "Chirality in Molecules Devoid of Chiral Centers (Chapter 14)". Stereochemistry of Organic Compounds (1st ed.). New York, NY, USA: Wiley & Sons. ISBN 978-0471016700. Retrieved 2 February 2016.

doi.org

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Chirality". doi:10.1351/goldbook.C01058
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Superposability". doi:10.1351/goldbook.S06144
Howland, Robert H. (July 2009). "Understanding chirality and stereochemistry: three-dimensional psychopharmacology". Journal of Psychosocial Nursing and Mental Health Services. 47 (7): 15–18. doi:10.3928/02793695-20090609-01. ISSN 0279-3695. PMID 19678474.
^ Streitwieser, A. Jr.; Wolfe, J. R. Jr.; Schaeffer, W. D. (1959). "Stereochemistry of the Primary Carbon. X. Stereochemical Configurations of Some Optically Active Deuterium Compounds". Tetrahedron. 6 (4): 338–344. doi:10.1016/0040-4020(59)80014-4.
Gal, Joseph (2012). "The Discovery of Stereoselectivity at Biological Receptors: Arnaldo Piutti and the Taste of the Asparagine Enantiomers-History and Analysis on the 125th Anniversary". Chirality. 24 (12): 959–976. doi:10.1002/chir.22071. PMID 23034823.
Theodore J. Leitereg; Dante G. Guadagni; Jean Harris; Thomas R. Mon; Roy Teranishi (1971). "Chemical and sensory data supporting the difference between the odors of the enantiomeric carvones". J. Agric. Food Chem. 19 (4): 785–787. Bibcode:1971JAFC...19..785L. doi:10.1021/jf60176a035.
Lepola U, Wade A, Andersen HF (May 2004). "Do equivalent doses of escitalopram and citalopram have similar efficacy? A pooled analysis of two positive placebo-controlled studies in major depressive disorder". Int Clin Psychopharmacol. 19 (3): 149–55. doi:10.1097/00004850-200405000-00005. PMID 15107657. S2CID 36768144.
Hyttel, J.; Bøgesø, K. P.; Perregaard, J.; Sánchez, C. (1992). "The pharmacological effect of citalopram resides in the (S)-(+)-enantiomer". Journal of Neural Transmission. 88 (2): 157–160. doi:10.1007/BF01244820. PMID 1632943. S2CID 20110906.
JAFFE, IA; ALTMAN, K; MERRYMAN, P (Oct 1964). "The Antipyridoxine Effect of Penicillamine in Man". The Journal of Clinical Investigation. 43 (10): 1869–73. doi:10.1172/JCI105060. PMC 289631. PMID 14236210.
Meierhenrich Uwe J., Nahon Laurent, Alcaraz Christian, Hendrik Bredehöft Jan, Hoffmann Søren V., Barbier Bernard, Brack André (2005). "Asymmetric Vacuum UV photolysis of the Amino Acid Leucine in the Solid State". Angew. Chem. Int. Ed. 44 (35): 5630–5634. doi:10.1002/anie.200501311. PMID 16035020.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Srinivasarao, M. (1999). "Chirality and Polymers". Current Opinion in Colloid & Interface Science. 4 (5): 369–376. doi:10.1016/S1359-0294(99)00024-2.
Bhushan, R.; Tanwar, S. J. Chromatogr. A 2010, 1395–1398. (doi:10.1016/j.chroma.2009.12.071)
Ravi Bhushan Chem. Rec. 2022, e102100295. (doi:10.1002/tcr.202100295)
Eliel, E.L. (1997). "Infelicitous Stereochemical Nomenclatures". Chirality. 9 (56): 428–430. doi:10.1002/(sici)1520-636x(1997)9:5/6<428::aid-chir5>3.3.co;2-e. Archived from the original on 3 March 2016. Retrieved 5 February 2016.
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "asymmetric synthesis". doi:10.1351/goldbook.E02072
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "enantiomerically enriched (enantioenriched)". doi:10.1351/goldbook.E02071
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "enantiomer excess (enantiomeric excess)". doi:10.1351/goldbook.E02070
Frankel, Eugene (1976). "Corpuscular Optics and the Wave Theory of Light: The Science and Politics of a Revolution in Physics". Social Studies of Science. 6 (2). Sage Publications Inc.: 147–154. doi:10.1177/030631277600600201. JSTOR 284930. S2CID 122887123.
Bentley, Ronald (1995). "From Optical Activity in Quartz to Chiral Drugs: Molecular Handedness in Biology and Medicine". Perspect. Biol. Med. 38 (2): 188–229. doi:10.1353/pbm.1995.0069. PMID 7899056. S2CID 46514372.
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Optical isomers". doi:10.1351/goldbook.O04308
Werner, A. (May 1911). "Zur Kenntnis des asymmetrischen Kobaltatoms. I". Berichte der Deutschen Chemischen Gesellschaft (in German). 44 (2): 1887–1898. doi:10.1002/cber.19110440297.
Friedman, L.; Miller, J. G. (1971). "Odor Incongruity and Chirality". Science. 172 (3987): 1044–1046. Bibcode:1971Sci...172.1044F. doi:10.1126/science.172.3987.1044. PMID 5573954. S2CID 25725148.
Ohloff, Günther; Vial, Christian; Wolf, Hans Richard; Job, Kurt; Jégou, Elise; Polonsky, Judith; Lederer, Edgar (1980). "Stereochemistry-Odor Relationships in Enantiomeric Ambergris Fragrances". Helvetica Chimica Acta. 63 (7): 1932–1946. doi:10.1002/hlca.19800630721.

harvard.edu

ui.adsabs.harvard.edu

Theodore J. Leitereg; Dante G. Guadagni; Jean Harris; Thomas R. Mon; Roy Teranishi (1971). "Chemical and sensory data supporting the difference between the odors of the enantiomeric carvones". J. Agric. Food Chem. 19 (4): 785–787. Bibcode:1971JAFC...19..785L. doi:10.1021/jf60176a035.
Friedman, L.; Miller, J. G. (1971). "Odor Incongruity and Chirality". Science. 172 (3987): 1044–1046. Bibcode:1971Sci...172.1044F. doi:10.1126/science.172.3987.1044. PMID 5573954. S2CID 25725148.

iupac.org

goldbook.iupac.org

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Chirality". doi:10.1351/goldbook.C01058
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Superposability". doi:10.1351/goldbook.S06144
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "asymmetric synthesis". doi:10.1351/goldbook.E02072
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "enantiomerically enriched (enantioenriched)". doi:10.1351/goldbook.E02071
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "enantiomer excess (enantiomeric excess)". doi:10.1351/goldbook.E02070
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Optical isomers". doi:10.1351/goldbook.O04308

jstor.org

Frankel, Eugene (1976). "Corpuscular Optics and the Wave Theory of Light: The Science and Politics of a Revolution in Physics". Social Studies of Science. 6 (2). Sage Publications Inc.: 147–154. doi:10.1177/030631277600600201. JSTOR 284930. S2CID 122887123.

newscientist.com

McKee, Maggie (2005-08-24). "Space radiation may select amino acids for life". New Scientist. Retrieved 2016-02-05.

nih.gov

pubmed.ncbi.nlm.nih.gov

Howland, Robert H. (July 2009). "Understanding chirality and stereochemistry: three-dimensional psychopharmacology". Journal of Psychosocial Nursing and Mental Health Services. 47 (7): 15–18. doi:10.3928/02793695-20090609-01. ISSN 0279-3695. PMID 19678474.
Gal, Joseph (2012). "The Discovery of Stereoselectivity at Biological Receptors: Arnaldo Piutti and the Taste of the Asparagine Enantiomers-History and Analysis on the 125th Anniversary". Chirality. 24 (12): 959–976. doi:10.1002/chir.22071. PMID 23034823.
Lepola U, Wade A, Andersen HF (May 2004). "Do equivalent doses of escitalopram and citalopram have similar efficacy? A pooled analysis of two positive placebo-controlled studies in major depressive disorder". Int Clin Psychopharmacol. 19 (3): 149–55. doi:10.1097/00004850-200405000-00005. PMID 15107657. S2CID 36768144.
Hyttel, J.; Bøgesø, K. P.; Perregaard, J.; Sánchez, C. (1992). "The pharmacological effect of citalopram resides in the (S)-(+)-enantiomer". Journal of Neural Transmission. 88 (2): 157–160. doi:10.1007/BF01244820. PMID 1632943. S2CID 20110906.
JAFFE, IA; ALTMAN, K; MERRYMAN, P (Oct 1964). "The Antipyridoxine Effect of Penicillamine in Man". The Journal of Clinical Investigation. 43 (10): 1869–73. doi:10.1172/JCI105060. PMC 289631. PMID 14236210.
Meierhenrich Uwe J., Nahon Laurent, Alcaraz Christian, Hendrik Bredehöft Jan, Hoffmann Søren V., Barbier Bernard, Brack André (2005). "Asymmetric Vacuum UV photolysis of the Amino Acid Leucine in the Solid State". Angew. Chem. Int. Ed. 44 (35): 5630–5634. doi:10.1002/anie.200501311. PMID 16035020.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Bentley, Ronald (1995). "From Optical Activity in Quartz to Chiral Drugs: Molecular Handedness in Biology and Medicine". Perspect. Biol. Med. 38 (2): 188–229. doi:10.1353/pbm.1995.0069. PMID 7899056. S2CID 46514372.
Friedman, L.; Miller, J. G. (1971). "Odor Incongruity and Chirality". Science. 172 (3987): 1044–1046. Bibcode:1971Sci...172.1044F. doi:10.1126/science.172.3987.1044. PMID 5573954. S2CID 25725148.

ncbi.nlm.nih.gov

JAFFE, IA; ALTMAN, K; MERRYMAN, P (Oct 1964). "The Antipyridoxine Effect of Penicillamine in Man". The Journal of Clinical Investigation. 43 (10): 1869–73. doi:10.1172/JCI105060. PMC 289631. PMID 14236210.

semanticscholar.org

api.semanticscholar.org

Lepola U, Wade A, Andersen HF (May 2004). "Do equivalent doses of escitalopram and citalopram have similar efficacy? A pooled analysis of two positive placebo-controlled studies in major depressive disorder". Int Clin Psychopharmacol. 19 (3): 149–55. doi:10.1097/00004850-200405000-00005. PMID 15107657. S2CID 36768144.
Hyttel, J.; Bøgesø, K. P.; Perregaard, J.; Sánchez, C. (1992). "The pharmacological effect of citalopram resides in the (S)-(+)-enantiomer". Journal of Neural Transmission. 88 (2): 157–160. doi:10.1007/BF01244820. PMID 1632943. S2CID 20110906.
Frankel, Eugene (1976). "Corpuscular Optics and the Wave Theory of Light: The Science and Politics of a Revolution in Physics". Social Studies of Science. 6 (2). Sage Publications Inc.: 147–154. doi:10.1177/030631277600600201. JSTOR 284930. S2CID 122887123.
Bentley, Ronald (1995). "From Optical Activity in Quartz to Chiral Drugs: Molecular Handedness in Biology and Medicine". Perspect. Biol. Med. 38 (2): 188–229. doi:10.1353/pbm.1995.0069. PMID 7899056. S2CID 46514372.
Friedman, L.; Miller, J. G. (1971). "Odor Incongruity and Chirality". Science. 172 (3987): 1044–1046. Bibcode:1971Sci...172.1044F. doi:10.1126/science.172.3987.1044. PMID 5573954. S2CID 25725148.

uottawa.ca

Eliel, E.L. (1997). "Infelicitous Stereochemical Nomenclatures". Chirality. 9 (56): 428–430. doi:10.1002/(sici)1520-636x(1997)9:5/6<428::aid-chir5>3.3.co;2-e. Archived from the original on 3 March 2016. Retrieved 5 February 2016.

web.archive.org

Eliel, E.L. (1997). "Infelicitous Stereochemical Nomenclatures". Chirality. 9 (56): 428–430. doi:10.1002/(sici)1520-636x(1997)9:5/6<428::aid-chir5>3.3.co;2-e. Archived from the original on 3 March 2016. Retrieved 5 February 2016.

wiley.com

doi.wiley.com

Werner, A. (May 1911). "Zur Kenntnis des asymmetrischen Kobaltatoms. I". Berichte der Deutschen Chemischen Gesellschaft (in German). 44 (2): 1887–1898. doi:10.1002/cber.19110440297.

worldcat.org

search.worldcat.org

Howland, Robert H. (July 2009). "Understanding chirality and stereochemistry: three-dimensional psychopharmacology". Journal of Psychosocial Nursing and Mental Health Services. 47 (7): 15–18. doi:10.3928/02793695-20090609-01. ISSN 0279-3695. PMID 19678474.