Chiralita (chémia) (Slovak Wikipedia)

Analysis of information sources in references of the Wikipedia article "Chiralita (chémia)" in Slovak language version.

refsWebsite

Global rank Slovak rank

20doi.org

2^nd place

7^th place

7nih.gov

4^th place

21^st place

6iupac.org

538^th place

298^th place

3web.archive.org

1^st place

8^th place

2stuba.sk

low place

115^th place

1prolekare.cz

low place

2,545^th place

1muni.cz

2,963^rd place

77^th place

1drugs.com

399^th place

1,392^nd place

1newscientist.com

774^th place

838^th place

1elsevier.com

610^th place

631^st place

1uottawa.ca

9,033^rd place

9,213^th place

1jstor.org

26^th place

384^th place

1wiley.com

222^nd place

174^th place

doi.org

dx.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
↑ Stereochemistry of the Primary Carbon. X. Stereochemical Configurations of Some Optically Active Deuterium Compounds. Tetrahedron, 1959, s. 338–344. DOI: 10.1016/0040-4020(59)80014-4.
GAL, Joseph. The Discovery of Stereoselectivity at Biological Receptors: Arnaldo Piutti and the Taste of the Asparagine Enantiomers-History and Analysis on the 125th Anniversary. Chirality, 2012, s. 959–976. DOI: 10.1002/chir.22071. PMID 23034823.
Chemical and sensory data supporting the difference between the odors of the enantiomeric carvones. J. Agric. Food Chem., 1971, s. 785–787. DOI: 10.1021/jf60176a035.
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, May 2004, s. 149–55. DOI: 10.1097/00004850-200405000-00005. PMID 15107657.
HYTTEL, J.; Bøgesø, K. P.; Perregaard, J.. The pharmacological effect of citalopram resides in the (S)-(+)-enantiomer. Journal of Neural Transmission, 1992, s. 157–160. DOI: 10.1007/BF01244820. PMID 1632943.
JAFFE, IA; ALTMAN, K; MERRYMAN, P. The Antipyridoxine Effect of Penicillamine in Man.. The Journal of Clinical Investigation, Oct 1964, s. 1869–73. DOI: 10.1172/JCI105060. PMID 14236210.
Meierhenrich Uwe J., Nahon Laurent, Alcaraz Christian, Hendrik Bredehöft Jan, Hoffmann Søren V., Barbier Bernard, Brack André. Asymmetric Vacuum UV photolysis of the Amino Acid Leucine in the Solid State. Angew. Chem. Int. Ed., 2005, s. 5630–5634. DOI: 10.1002/anie.200501311. PMID 16035020.
Chemical and sensory data supporting the difference between the odors of the enantiomeric carvones. J. Agric. Food Chem., 1971, s. 785–787. DOI: 10.1021/jf60176a035.
SRINIVASARAO, Mohan. Chirality and polymers. Current Opinion in Colloid & Interface Science, 1999-04, roč. 4, čís. 2, s. 147–152. Dostupné online [cit. 2022-04-09]. DOI: 10.1016/S1359-0294(99)00024-2. (po anglicky)
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "enantiomerically enriched (enantioenriched)". DOI:10.1351/goldbook.E02071
Eliel, E.L.. Infelicitous Stereochemical Nomenclatures. Chirality, 1997, s. 428–430. Dostupné online [cit. 2016-02-05]. DOI: 10.1002/(sici)1520-636x(1997)9:5/6<428::aid-chir5>3.3.co;2-e. Archivované 2016-03-03 na Wayback Machine
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–) "enantiomer excess (enantiomeric excess)". DOI:10.1351/goldbook.E02070
Bentley, Ronald. From Optical Activity in Quartz to Chiral Drugs: Molecular Handedness in Biology and Medicine.. Perspect. Biol. Med., 1995, s. 188–229. DOI: 10.1353/pbm.1995.0069. PMID 7899056.
IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Optical isomers". DOI:10.1351/goldbook.O04308
WERNER, A.. Zur Kenntnis des asymmetrischen Kobaltatoms. I. Berichte der Deutschen Chemischen Gesellschaft, May 1911, s. 1887–1898. Dostupné online. DOI: 10.1002/cber.19110440297. (po nemecky)
Odor Incongruity and Chirality. Science, 1971, s. 1044–1046. DOI: 10.1126/science.172.3987.1044. PMID 5573954.
Stereochemistry-Odor Relationships in Enantiomeric Ambergris Fragrances. Helvetica Chimica Acta, 1980, s. 1932–1946. DOI: 10.1002/hlca.19800630721.

drugs.com

Escitalopram Monograph for Professionals [online]. Drugs.com, [cit. 2022-04-09]. Dostupné online. (po anglicky)

elsevier.com

linkinghub.elsevier.com

SRINIVASARAO, Mohan. Chirality and polymers. Current Opinion in Colloid & Interface Science, 1999-04, roč. 4, čís. 2, s. 147–152. Dostupné online [cit. 2022-04-09]. DOI: 10.1016/S1359-0294(99)00024-2. (po anglicky)

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–) "enantiomerically enriched (enantioenriched)". DOI:10.1351/goldbook.E02071
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–) "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. Corpuscular Optics and the Wave Theory of Light: The Science and Politics of a Revolution in Physics. Social Studies of Science (Sage Publications Inc.), 1976, s. 147–154. Dostupné online.

muni.cz

is.muni.cz

Symetrie molekul [online]. is.muni.cz, [cit. 2022-04-09]. Dostupné online.

newscientist.com

MCKEE, Maggie. Space radiation may select amino acids for life [online]. New Scientist, [cit. 2016-02-05]. Dostupné online. (po anglicky)

nih.gov

ncbi.nlm.nih.gov

GAL, Joseph. The Discovery of Stereoselectivity at Biological Receptors: Arnaldo Piutti and the Taste of the Asparagine Enantiomers-History and Analysis on the 125th Anniversary. Chirality, 2012, s. 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, May 2004, s. 149–55. DOI: 10.1097/00004850-200405000-00005. PMID 15107657.
HYTTEL, J.; Bøgesø, K. P.; Perregaard, J.. The pharmacological effect of citalopram resides in the (S)-(+)-enantiomer. Journal of Neural Transmission, 1992, s. 157–160. DOI: 10.1007/BF01244820. PMID 1632943.
JAFFE, IA; ALTMAN, K; MERRYMAN, P. The Antipyridoxine Effect of Penicillamine in Man.. The Journal of Clinical Investigation, Oct 1964, s. 1869–73. DOI: 10.1172/JCI105060. PMID 14236210.
Meierhenrich Uwe J., Nahon Laurent, Alcaraz Christian, Hendrik Bredehöft Jan, Hoffmann Søren V., Barbier Bernard, Brack André. Asymmetric Vacuum UV photolysis of the Amino Acid Leucine in the Solid State. Angew. Chem. Int. Ed., 2005, s. 5630–5634. DOI: 10.1002/anie.200501311. PMID 16035020.
Bentley, Ronald. From Optical Activity in Quartz to Chiral Drugs: Molecular Handedness in Biology and Medicine.. Perspect. Biol. Med., 1995, s. 188–229. DOI: 10.1353/pbm.1995.0069. PMID 7899056.
Odor Incongruity and Chirality. Science, 1971, s. 1044–1046. DOI: 10.1126/science.172.3987.1044. PMID 5573954.

prolekare.cz

MORAVČÍK, Jakub; HROBOŇOVÁ, Katarína. Separácia enantiomérov aminokyselín metódou vysokoúčinnej kvapalinovej chromatografie [online]. www.prolekare.cz, [cit. 2022-04-09]. Dostupné online.

stuba.sk

schs.chtf.stuba.sk

PUTALA, Martin. NIEKTORÉ ZMENY V NÁZVOSLOVÍ ORGANICKÝCH ZLÚČENÍN [online]. 2008-02-08, [cit. 2022-04-09]. Dostupné online. Archivované 2007-06-23 z originálu.
PUTALA, Martin. NIEKTORÉ ZMENY V NÁZVOSLOVÍ ORGANICKÝCH ZLÚČENÍN [online]. 2008-02-08, [cit. 2022-04-09]. Dostupné online. Archivované 2007-06-23 z originálu.

uottawa.ca

Eliel, E.L.. Infelicitous Stereochemical Nomenclatures. Chirality, 1997, s. 428–430. Dostupné online [cit. 2016-02-05]. DOI: 10.1002/(sici)1520-636x(1997)9:5/6<428::aid-chir5>3.3.co;2-e. Archivované 2016-03-03 na Wayback Machine

web.archive.org

PUTALA, Martin. NIEKTORÉ ZMENY V NÁZVOSLOVÍ ORGANICKÝCH ZLÚČENÍN [online]. 2008-02-08, [cit. 2022-04-09]. Dostupné online. Archivované 2007-06-23 z originálu.
Eliel, E.L.. Infelicitous Stereochemical Nomenclatures. Chirality, 1997, s. 428–430. Dostupné online [cit. 2016-02-05]. DOI: 10.1002/(sici)1520-636x(1997)9:5/6<428::aid-chir5>3.3.co;2-e. Archivované 2016-03-03 na Wayback Machine
PUTALA, Martin. NIEKTORÉ ZMENY V NÁZVOSLOVÍ ORGANICKÝCH ZLÚČENÍN [online]. 2008-02-08, [cit. 2022-04-09]. Dostupné online. Archivované 2007-06-23 z originálu.

wiley.com

doi.wiley.com

WERNER, A.. Zur Kenntnis des asymmetrischen Kobaltatoms. I. Berichte der Deutschen Chemischen Gesellschaft, May 1911, s. 1887–1898. Dostupné online. DOI: 10.1002/cber.19110440297. (po nemecky)