Asymetrická syntéza (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Asymetrická syntéza" in Czech language version.

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  • LE BEL, Joseph. Sur les relations qui existent entre les formules atomiques des corps organiques et le pouvoir rotatoire de leurs dissolutions. Bull. Soc. Chim. Fr. 1874, s. 337-347. Dostupné online. 

doi.org

dx.doi.org

  • 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. 
  • Theodore J. Leitereg; DANTE G. GUADAGNI; JEAN HARRIS; THOMAS R. MON; ROY TERANISHI. 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. 
  • Lepola U, Wade A, Andersen HF. 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 10.1097/01.yic.0000122862.35081.cd. PMID 15107657. 
  • HYTTEL, J.; BØGESØ, K. P.; PERREGAARD, J.; SÁNCHEZ, C. 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. 
  • M. Heitbaum; F. GLORIUS; I. ESCHER. Asymmetric Heterogeneous Catalysis. Angewandte Chemie International Edition. 2006, s. 4732–4762. DOI 10.1002/anie.200504212. PMID 16802397. 
  • Glorius, F.; GNAS, Y. Chiral Auxiliaries – Principles and Recent Applications. Synthesis. 2006, s. 1899–1930. DOI 10.1055/s-2006-942399. 
  • SCHMID, A.; DORDICK, J. S.; HAUER, B.; KIENER, A.; WUBBOLTS, M.; WITHOLT, B. Industrial biocatalysis today and tomorrow. Nature. 2001, s. 258–268. DOI 10.1038/35051736. PMID 11196655. 
  • MÜLLER, Michael. Chemoenzymatic Synthesis of Building Blocks for Statin Side Chains. Angewandte Chemie International Edition. 7 January 2005, s. 362–365. DOI 10.1002/anie.200460852. PMID 15593081. 
  • LIST, Benjamin. Organocatalysis. Chem. Rev.. 2007, s. 5413–5883. DOI 10.1021/cr078412e. 
  • DALKO, Peter I.; MOISAN, LIONEL. Enantioselective Organocatalysis. Angewandte Chemie International Edition. 15 October 2001, s. 3726–3748. DOI 10.1002/1521-3773(20011015)40:20<3726::AID-ANIE3726>3.0.CO;2-D. 
  • NOTZ, Wolfgang; TANAKA, FUJIE; BARBAS, CARLOS F. Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels−Alder Reactions. Accounts of Chemical Research. 1 August 2004, s. 580–591. DOI 10.1021/ar0300468. PMID 15311957. 
  • BERTELSEN, Søren; JØRGENSEN, Karl Anker. Organocatalysis—after the gold rush. Chemical Society Reviews. 2009, s. 2178–89. DOI 10.1039/b903816g. PMID 19623342. 
  • Pedro Cintas. Tracing the Origins and Evolution of Chirality and Handedness in Chemical Language. Angewandte Chemie International Edition. 2007, s. 4016–4024. DOI 10.1002/anie.200603714. PMID 17328087. 
  • FISCHER, Emil. Synthesen in der Zuckergruppe II. Berichte der deutschen chemischen Gesellschaft. 1 October 1894, s. 3189–3232. DOI 10.1002/cber.189402703109. 
  • FISCHER, Emil; HIRSCHBERGER, JOSEF. Ueber Mannose. II. Berichte der deutschen chemischen Gesellschaft. 1 January 1889, s. 365–376. DOI 10.1002/cber.18890220183. 
  • Marckwald, W. Ueber asymmetrische Synthese. Berichte der deutschen chemischen Gesellschaft. 1904, s. 349–354. DOI 10.1002/cber.19040370165. 
  • CAMPBELL, Chantel D.; VEDERAS, John C. Biosynthesis of lovastatin and related metabolites formed by fungal iterative PKS enzymes. Biopolymers. 23 June 2010, s. 755–763. DOI 10.1002/bip.21428. 
  • BIJVOET, J. M.; PEERDEMAN, A. F.; VAN BOMMEL, A. J. Determination of the Absolute Configuration of Optically Active Compounds by Means of X-Rays. Nature. 1951, s. 271–272. DOI 10.1038/168271a0. Bibcode 1951Natur.168..271B. 
  • DALGLIESH, C. E. 756. The optical resolution of aromatic amino-acids on paper chromatograms. Journal of the Chemical Society (Resumed). 1952, s. 3940. DOI 10.1039/JR9520003940. 
  • KLEMM, L.H.; REED, DAVID. Optical resolution by molecular complexation chromatography. Journal of Chromatography A. 1960, s. 364–368. DOI 10.1016/S0021-9673(01)97011-6. 
  • CUSHNY, AR. Atropine and the hyoscyamines-a study of the action of optical isomers. The Journal of Physiology. 2 November 1903, s. 176–94. DOI 10.1113/jphysiol.1903.sp000988. PMID 16992694. 
  • CUSHNY, AR; PEEBLES, AR. The action of optical isomers: II. Hyoscines. The Journal of Physiology. 13 July 1905, s. 501–10. DOI 10.1113/jphysiol.1905.sp001097. PMID 16992790. 
  • MCBRIDE, W. G. Thalidomide and Congenital Abnormalities. The Lancet. 1961, s. 1358. DOI 10.1016/S0140-6736(61)90927-8. 
  • Robert Sidney Cahn; Christopher Kelk Ingold; Vladimir Prelog. Specification of Molecular Chirality. Angewandte Chemie International Edition. 1966, s. 385–415. DOI 10.1002/anie.196603851. 
  • Vladimir Prelog; Günter Helmchen. Basic Principles of the CIP-System and Proposals for a Revision. Angewandte Chemie International Edition. 1982, s. 567–583. DOI 10.1002/anie.198205671. 
  • GIL-AV, Emanuel; FEIBUSH, BINYAMIN; CHARLES-SIGLER, ROSITA. Separation of enantiomers by gas liquid chromatography with an optically active stationary phase. Tetrahedron Letters. 1966, s. 1009–1015. DOI 10.1016/S0040-4039(00)70231-0. 
  • VINEYARD, B. D.; KNOWLES, W. S.; SABACKY, M. J.; BACHMAN, G. L.; WEINKAUFF, D. J. Asymmetric hydrogenation. Rhodium chiral bisphosphine catalyst. Journal of the American Chemical Society. 1977, s. 5946–5952. DOI 10.1021/ja00460a018. 
  • KNOWLES, William S. Asymmetric Hydrogenations (Nobel Lecture). Angewandte Chemie International Edition. 2002, s. 1998. DOI 10.1002/1521-3773(20020617)41:12<1998::AID-ANIE1998>3.0.CO;2-8. 
  • KNOWLES, W. S. Application of organometallic catalysis to the commercial production of L-DOPA. Journal of Chemical Education. March 1986, s. 222. DOI 10.1021/ed063p222. Bibcode 1986JChEd..63..222K. 
  • H. Nozaki; H. TAKAYA; S. MORIUTI; R. NOYORI. Homogeneous catalysis in the decomposition of diazo compounds by copper chelates: Asymmetric carbenoid reactions. Tetrahedron. 1968, s. 3655–3669. DOI 10.1016/S0040-4020(01)91998-2. 
  • KATSUKI, Tsutomu; SHARPLESS, K. BARRY. The first practical method for asymmetric epoxidation. Journal of the American Chemical Society. 1980, s. 5974–5976. DOI 10.1021/ja00538a077. 
  • JACOBSEN, Eric N.; MARKO, ISTVAN.; MUNGALL, WILLIAM S.; SCHROEDER, GEORG.; SHARPLESS, K. BARRY. Asymmetric dihydroxylation via ligand-accelerated catalysis. Journal of the American Chemical Society. 1988, s. 1968–1970. DOI 10.1021/ja00214a053. 
  • SHARPLESS, K. Barry; PATRICK, DONALD W.; TRUESDALE, LARRY K.; BILLER, SCOTT A. New reaction. Stereospecific vicinal oxyamination of olefins by alkyl imido osmium compounds. Journal of the American Chemical Society. 1975, s. 2305–2307. DOI 10.1021/ja00841a071. 
  • J. A. Dale, D. L. Dull and H. S. Mosher. α-Methoxy-α-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines. J. Org. Chem.. 1969, s. 2543–2549. DOI 10.1021/jo01261a013. 
  • HINCKLEY, Conrad C. Paramagnetic shifts in solutions of cholesterol and the dipyridine adduct of trisdipivalomethanatoeuropium(III). A shift reagent. Journal of the American Chemical Society. 1969, s. 5160–5162. DOI 10.1021/ja01046a038. PMID 5798101. 
  • ENSLEY, Harry E.; PARNELL, CAROL A.; COREY, ELIAS J. Convenient synthesis of a highly efficient and recyclable chiral director for asymmetric induction. The Journal of Organic Chemistry. 1978, s. 1610–1612. DOI 10.1021/jo00402a037. 
  • SARIASLANI, F.Sima; ROSAZZA, JOHN P.N. Biocatalysis in natural products chemistry. Enzyme and Microbial Technology. 1984, s. 242–253. DOI 10.1016/0141-0229(84)90125-X. 
  • WANDREY, Christian; LIESE, ANDREAS; KIHUMBU, DAVID. Industrial Biocatalysis: Past, Present, and Future. Organic Process Research & Development. 2000, s. 286–290. DOI 10.1021/op990101l. 

harvard.edu

adsabs.harvard.edu

  • BIJVOET, J. M.; PEERDEMAN, A. F.; VAN BOMMEL, A. J. Determination of the Absolute Configuration of Optically Active Compounds by Means of X-Rays. Nature. 1951, s. 271–272. DOI 10.1038/168271a0. Bibcode 1951Natur.168..271B. 
  • KNOWLES, W. S. Application of organometallic catalysis to the commercial production of L-DOPA. Journal of Chemical Education. March 1986, s. 222. DOI 10.1021/ed063p222. Bibcode 1986JChEd..63..222K. 

hathitrust.org

babel.hathitrust.org

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. 
  • Lepola U, Wade A, Andersen HF. 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 10.1097/01.yic.0000122862.35081.cd. PMID 15107657. 
  • HYTTEL, J.; BØGESØ, K. P.; PERREGAARD, J.; SÁNCHEZ, C. 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. 
  • M. Heitbaum; F. GLORIUS; I. ESCHER. Asymmetric Heterogeneous Catalysis. Angewandte Chemie International Edition. 2006, s. 4732–4762. DOI 10.1002/anie.200504212. PMID 16802397. 
  • SCHMID, A.; DORDICK, J. S.; HAUER, B.; KIENER, A.; WUBBOLTS, M.; WITHOLT, B. Industrial biocatalysis today and tomorrow. Nature. 2001, s. 258–268. DOI 10.1038/35051736. PMID 11196655. 
  • MÜLLER, Michael. Chemoenzymatic Synthesis of Building Blocks for Statin Side Chains. Angewandte Chemie International Edition. 7 January 2005, s. 362–365. DOI 10.1002/anie.200460852. PMID 15593081. 
  • NOTZ, Wolfgang; TANAKA, FUJIE; BARBAS, CARLOS F. Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels−Alder Reactions. Accounts of Chemical Research. 1 August 2004, s. 580–591. DOI 10.1021/ar0300468. PMID 15311957. 
  • BERTELSEN, Søren; JØRGENSEN, Karl Anker. Organocatalysis—after the gold rush. Chemical Society Reviews. 2009, s. 2178–89. DOI 10.1039/b903816g. PMID 19623342. 
  • Pedro Cintas. Tracing the Origins and Evolution of Chirality and Handedness in Chemical Language. Angewandte Chemie International Edition. 2007, s. 4016–4024. DOI 10.1002/anie.200603714. PMID 17328087. 
  • CUSHNY, AR. Atropine and the hyoscyamines-a study of the action of optical isomers. The Journal of Physiology. 2 November 1903, s. 176–94. DOI 10.1113/jphysiol.1903.sp000988. PMID 16992694. 
  • CUSHNY, AR; PEEBLES, AR. The action of optical isomers: II. Hyoscines. The Journal of Physiology. 13 July 1905, s. 501–10. DOI 10.1113/jphysiol.1905.sp001097. PMID 16992790. 
  • HINCKLEY, Conrad C. Paramagnetic shifts in solutions of cholesterol and the dipyridine adduct of trisdipivalomethanatoeuropium(III). A shift reagent. Journal of the American Chemical Society. 1969, s. 5160–5162. DOI 10.1021/ja01046a038. PMID 5798101.