Χειρομορφία (χημεία) (Greek Wikipedia)

Analysis of information sources in references of the Wikipedia article "Χειρομορφία (χημεία)" in Greek language version.

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17doi.org

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9nih.gov

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6iupac.org

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4harvard.edu

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57^th place

3archive.org

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1worldcat.org

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1newscientist.com

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1uottawa.ca

9,033^rd place

low place

1jstor.org

26^th place

139^th place

1books.google.com

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1wiley.com

222^nd place

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archive.org (Global: 6^th place; Greek: 5^th place)

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. PMID 14236210. PMC 289631. https://archive.org/details/sim_journal-of-clinical-investigation_1964-10_43_10/page/1868.
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. https://archive.org/details/sim_perspectives-in-biology-and-medicine_winter-1995_38_2/page/188.
Friedman, L.; Miller, J. G. (1971). «Odor Incongruity and Chirality». Science 172 (3987): 1044–1046. doi:10.1126/science.172.3987.1044. PMID 5573954. Bibcode: 1971Sci...172.1044F. https://archive.org/details/sim_science_1971-06-04_172_3987/page/1044.

books.google.com (Global: 3^rd place; Greek: 6^th place)

Eliel, Ernest Ludwig· Wilen, Samuel H.· Mander, Lewis N. (1994). «Chirality in Molecules Devoid of Chiral Centers (Chapter 14)». Stereochemistry of Organic Compounds (1st έκδοση). New York, NY, USA: Wiley & Sons. ISBN 978-0471016700. Ανακτήθηκε στις 2 Φεβρουαρίου 2016.

doi.org (Global: 2^nd place; Greek: 3^rd place)

dx.doi.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.
^ 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. doi:10.1021/jf60176a035. Bibcode: 1971JAFC...19..785L.
«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. May 2004. doi:10.1097/00004850-200405000-00005. PMID 15107657.
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.
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. PMID 14236210. PMC 289631. https://archive.org/details/sim_journal-of-clinical-investigation_1964-10_43_10/page/1868.
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. Bibcode: 2005ACIE...44.5630M.
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. https://www.uottawa.ca/publications/interscientia/inter.4/eliel/eliel.html. Ανακτήθηκε στις 5 February 2016.
Frankel, Eugene (1976). «Corpuscular Optics and the Wave Theory of Light: The Science and Politics of a Revolution in Physics». Social Studies of Science (Sage Publications Inc.) 6 (2): 147–154. doi:10.1177/030631277600600201. https://www.jstor.org/stable/284930.
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. https://archive.org/details/sim_perspectives-in-biology-and-medicine_winter-1995_38_2/page/188.
Werner, A. (May 1911). «Zur Kenntnis des asymmetrischen Kobaltatoms. I» (στα γερμανικά). Berichte der Deutschen Chemischen Gesellschaft 44 (2): 1887–1898. doi:10.1002/cber.19110440297. http://doi.wiley.com/10.1002/cber.19110440297.
Friedman, L.; Miller, J. G. (1971). «Odor Incongruity and Chirality». Science 172 (3987): 1044–1046. doi:10.1126/science.172.3987.1044. PMID 5573954. Bibcode: 1971Sci...172.1044F. https://archive.org/details/sim_science_1971-06-04_172_3987/page/1044.
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. Bibcode: 1980HChAc..63.1932O.

harvard.edu (Global: 18^th place; Greek: 57^th place)

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. doi:10.1021/jf60176a035. Bibcode: 1971JAFC...19..785L.
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. Bibcode: 2005ACIE...44.5630M.
Friedman, L.; Miller, J. G. (1971). «Odor Incongruity and Chirality». Science 172 (3987): 1044–1046. doi:10.1126/science.172.3987.1044. PMID 5573954. Bibcode: 1971Sci...172.1044F. https://archive.org/details/sim_science_1971-06-04_172_3987/page/1044.
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. Bibcode: 1980HChAc..63.1932O.

iupac.org (Global: 538^th place; Greek: 757^th place)

goldbook.iupac.org

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Chirality".
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Superposability".
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "asymmetric synthesis".
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "enantiomerically enriched (enantioenriched)".
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "enantiomer excess (enantiomeric excess)".
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Optical isomers".

jstor.org (Global: 26^th place; Greek: 139^th place)

Frankel, Eugene (1976). «Corpuscular Optics and the Wave Theory of Light: The Science and Politics of a Revolution in Physics». Social Studies of Science (Sage Publications Inc.) 6 (2): 147–154. doi:10.1177/030631277600600201. https://www.jstor.org/stable/284930.

newscientist.com (Global: 774^th place; Greek: 684^th place)

McKee, Maggie (2005-08-24). «Space radiation may select amino acids for life». New Scientist. https://www.newscientist.com/article/dn7895-space-radiation-may-select-amino-acids-for-life.html. Ανακτήθηκε στις 2016-02-05.

nih.gov (Global: 4^th place; Greek: 4^th place)

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.
«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. May 2004. doi:10.1097/00004850-200405000-00005. PMID 15107657.
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.
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. PMID 14236210. PMC 289631. https://archive.org/details/sim_journal-of-clinical-investigation_1964-10_43_10/page/1868.
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. Bibcode: 2005ACIE...44.5630M.
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. https://archive.org/details/sim_perspectives-in-biology-and-medicine_winter-1995_38_2/page/188.
Friedman, L.; Miller, J. G. (1971). «Odor Incongruity and Chirality». Science 172 (3987): 1044–1046. doi:10.1126/science.172.3987.1044. PMID 5573954. Bibcode: 1971Sci...172.1044F. https://archive.org/details/sim_science_1971-06-04_172_3987/page/1044.

pubmedcentral.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. PMID 14236210. PMC 289631. https://archive.org/details/sim_journal-of-clinical-investigation_1964-10_43_10/page/1868.

uottawa.ca (Global: 9,033^rd place; Greek: low place)

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. https://www.uottawa.ca/publications/interscientia/inter.4/eliel/eliel.html. Ανακτήθηκε στις 5 February 2016.

wiley.com (Global: 222^nd place; Greek: 225^th place)

doi.wiley.com

Werner, A. (May 1911). «Zur Kenntnis des asymmetrischen Kobaltatoms. I» (στα γερμανικά). Berichte der Deutschen Chemischen Gesellschaft 44 (2): 1887–1898. doi:10.1002/cber.19110440297. http://doi.wiley.com/10.1002/cber.19110440297.

worldcat.org (Global: 5^th place; Greek: 8^th place)

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.

Χειρομορφία (χημεία) (Greek Wikipedia)

archive.org (Global: 6th place; Greek: 5th place)

books.google.com (Global: 3rd place; Greek: 6th place)

doi.org (Global: 2nd place; Greek: 3rd place)

dx.doi.org

harvard.edu (Global: 18th place; Greek: 57th place)

adsabs.harvard.edu

iupac.org (Global: 538th place; Greek: 757th place)