References analysis of the Wikipedia article "Enantioselective synthesis" in the English version

bnf.fr

gallica.bnf.fr

doi.org

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "asymmetric synthesis". doi:10.1351/goldbook.A00484

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "stereoselective synthesis". doi:10.1351/goldbook.S05990

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.

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 (October 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.

Smith, Silas W. (July 2009). "Chiral Toxicology: It's the Same Thing...Only Different". Toxicological Sciences. 110 (1): 4–30. doi:10.1093/toxsci/kfp097. PMID 19414517.

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "asymmetric induction". doi:10.1351/goldbook.A00483

Bauer, Eike B. (2012). "Chiral-at-metal complexes and their catalytic applications in organic synthesis". Chemical Society Reviews. 41 (8): 3153–67. doi:10.1039/C2CS15234G. PMID 22306968.

Zhang, Lilu; Meggers, Eric (21 February 2017). "Steering Asymmetric Lewis Acid Catalysis Exclusively with Octahedral Metal-Centered Chirality". Accounts of Chemical Research. 50 (2): 320–330. doi:10.1021/acs.accounts.6b00586. ISSN 0001-4842. PMID 28128920.

Huang, Xiaoqiang; Meggers, Eric (19 March 2019). "Asymmetric Photocatalysis with Bis-cyclometalated Rhodium Complexes". Accounts of Chemical Research. 52 (3): 833–847. doi:10.1021/acs.accounts.9b00028. ISSN 0001-4842. PMID 30840435. S2CID 73503362.

M. Heitbaum; F. Glorius; I. Escher (2006). "Asymmetric Heterogeneous Catalysis". Angewandte Chemie International Edition. 45 (29): 4732–4762. doi:10.1002/anie.200504212. PMID 16802397.

Glorius, F.; Gnas, Y. (2006). "Chiral Auxiliaries – Principles and Recent Applications". Synthesis. 2006 (12): 1899–1930. doi:10.1055/s-2006-942399.

IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Biocatalysis". doi:10.1351/goldbook.B00652

Schmid, A.; Dordick, J. S.; Hauer, B.; Kiener, A.; Wubbolts, M.; Witholt, B. (2001). "Industrial biocatalysis today and tomorrow". Nature. 409 (6817): 258–268. Bibcode:2001Natur.409..258S. doi:10.1038/35051736. PMID 11196655. S2CID 4340563.

Müller, Michael (7 January 2005). "Chemoenzymatic Synthesis of Building Blocks for Statin Side Chains". Angewandte Chemie International Edition. 44 (3): 362–365. doi:10.1002/anie.200460852. PMID 15593081.

Special Issue: List, Benjamin (2007). "Organocatalysis". Chem. Rev. 107 (12): 5413–5883. doi:10.1021/cr078412e.

Dalko, Peter I.; Moisan, Lionel (15 October 2001). "Enantioselective Organocatalysis". Angewandte Chemie International Edition. 40 (20): 3726–3748. doi:10.1002/1521-3773(20011015)40:20<3726::AID-ANIE3726>3.0.CO;2-D. PMID 11668532.

Notz, Wolfgang; Tanaka, Fujie; Barbas, Carlos F. (1 August 2004). "Enamine-Based Organocatalysis with Proline and Diamines: The Development of Direct Catalytic Asymmetric Aldol, Mannich, Michael, and Diels−Alder Reactions". Accounts of Chemical Research. 37 (8): 580–591. doi:10.1021/ar0300468. PMID 15311957.

Bertelsen, Søren; Jørgensen, Karl Anker (2009). "Organocatalysis—after the gold rush". Chemical Society Reviews. 38 (8): 2178–89. doi:10.1039/b903816g. PMID 19623342.

Snyder, Lloyd R.; Kirkland, Joseph J.; Glajch, Joseph L. (28 February 1997). Practical HPLC Method Development. doi:10.1002/9781118592014. ISBN 978-1-118-59201-4.

Gal, Joseph (January 2011). "Louis Pasteur, language, and molecular chirality. I. Background and Dissymmetry". Chirality. 23 (1): 1–16. doi:10.1002/chir.20866. PMID 20589938.

Pedro Cintas (2007). "Tracing the Origins and Evolution of Chirality and Handedness in Chemical Language". Angewandte Chemie International Edition. 46 (22): 4016–4024. doi:10.1002/anie.200603714. PMID 17328087.

Fischer, Emil (1 October 1894). "Synthesen in der Zuckergruppe II". Berichte der Deutschen Chemischen Gesellschaft. 27 (3): 3189–3232. doi:10.1002/cber.189402703109.

Fischer, Emil; Hirschberger, Josef (1 January 1889). "Ueber Mannose. II". Berichte der Deutschen Chemischen Gesellschaft. 22 (1): 365–376. doi:10.1002/cber.18890220183.

Marckwald, W. (1904). "Ueber asymmetrische Synthese". Berichte der Deutschen Chemischen Gesellschaft. 37: 349–354. doi:10.1002/cber.19040370165.

Campbell, Chantel D.; Vederas, John C. (23 June 2010). "Biosynthesis of lovastatin and related metabolites formed by fungal iterative PKS enzymes". Biopolymers. 93 (9): 755–763. doi:10.1002/bip.21428. PMID 20577995.

McKenzie, Alexander (1 January 1904). "CXXVII.Studies in asymmetric synthesis. I. Reduction of menthyl benzoylformate. II. Action of magnesium alkyl haloids on menthyl benzoylformate". J. Chem. Soc. Trans. 85: 1249–1262. doi:10.1039/CT9048501249.

Bijvoet, J. M.; Peerdeman, A. F.; van Bommel, A. J. (1951). "Determination of the Absolute Configuration of Optically Active Compounds by Means of X-Rays". Nature. 168 (4268): 271–272. Bibcode:1951Natur.168..271B. doi:10.1038/168271a0. S2CID 4264310.

Dalgliesh, C. E. (1952). "756. The optical resolution of aromatic amino-acids on paper chromatograms". Journal of the Chemical Society (Resumed): 3940. doi:10.1039/JR9520003940.

Klemm, L.H.; Reed, David (1960). "Optical resolution by molecular complexation chromatography". Journal of Chromatography A. 3: 364–368. doi:10.1016/S0021-9673(01)97011-6.

Cushny, AR (2 November 1903). "Atropine and the hyoscyamines-a study of the action of optical isomers". The Journal of Physiology. 30 (2): 176–94. doi:10.1113/jphysiol.1903.sp000988. PMC 1540678. PMID 16992694.

Cushny, AR; Peebles, AR (13 July 1905). "The action of optical isomers: II. Hyoscines". The Journal of Physiology. 32 (5–6): 501–10. doi:10.1113/jphysiol.1905.sp001097. PMC 1465734. PMID 16992790.

McBride, W. G. (1961). "Thalidomide and Congenital Abnormalities". The Lancet. 278 (7216): 1358. doi:10.1016/S0140-6736(61)90927-8.

Ito, Takumi; Ando, Hideki; Handa, Hiroshi (May 2011). "Teratogenic effects of thalidomide: molecular mechanisms". Cellular and Molecular Life Sciences. 68 (9): 1569–1579. doi:10.1007/s00018-010-0619-9. PMC 11114848. PMID 21207098. S2CID 12391084.

Robert Sidney Cahn; Christopher Kelk Ingold; Vladimir Prelog (1966). "Specification of Molecular Chirality". Angewandte Chemie International Edition. 5 (4): 385–415. doi:10.1002/anie.196603851.

Vladimir Prelog; Günter Helmchen (1982). "Basic Principles of the CIP-System and Proposals for a Revision". Angewandte Chemie International Edition. 21 (8): 567–583. doi:10.1002/anie.198205671.

Gil-Av, Emanuel; Feibush, Binyamin; Charles-Sigler, Rosita (1966). "Separation of enantiomers by gas liquid chromatography with an optically active stationary phase". Tetrahedron Letters. 7 (10): 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. (1977). "Asymmetric hydrogenation. Rhodium chiral bisphosphine catalyst". Journal of the American Chemical Society. 99 (18): 5946–5952. doi:10.1021/ja00460a018.

Knowles, William S. (2002). "Asymmetric Hydrogenations (Nobel Lecture)". Angewandte Chemie International Edition. 41 (12): 1999–2007. doi:10.1002/1521-3773(20020617)41:12<1998::AID-ANIE1998>3.0.CO;2-8. PMID 19746594.

Knowles, W. S. (March 1986). "Application of organometallic catalysis to the commercial production of L-DOPA". Journal of Chemical Education. 63 (3): 222. Bibcode:1986JChEd..63..222K. doi:10.1021/ed063p222.

H. Nozaki; H. Takaya; S. Moriuti; R. Noyori (1968). "Homogeneous catalysis in the decomposition of diazo compounds by copper chelates: Asymmetric carbenoid reactions". Tetrahedron. 24 (9): 3655–3669. doi:10.1016/S0040-4020(01)91998-2.

Katsuki, Tsutomu; Sharpless, K. Barry (1980). "The first practical method for asymmetric epoxidation". Journal of the American Chemical Society. 102 (18): 5974–5976. doi:10.1021/ja00538a077.

Jacobsen, Eric N.; Marko, Istvan.; Mungall, William S.; Schroeder, Georg.; Sharpless, K. Barry. (1988). "Asymmetric dihydroxylation via ligand-accelerated catalysis". Journal of the American Chemical Society. 110 (6): 1968–1970. doi:10.1021/ja00214a053.

Sharpless, K. Barry; Patrick, Donald W.; Truesdale, Larry K.; Biller, Scott A. (1975). "New reaction. Stereospecific vicinal oxyamination of olefins by alkyl imido osmium compounds". Journal of the American Chemical Society. 97 (8): 2305–2307. doi:10.1021/ja00841a071.

J. A. Dale, D. L. Dull and H. S. Mosher (1969). "α-Methoxy-α-trifluoromethylphenylacetic acid, a versatile reagent for the determination of enantiomeric composition of alcohols and amines". J. Org. Chem. 34 (9): 2543–2549. doi:10.1021/jo01261a013.

Hinckley, Conrad C. (1969). "Paramagnetic shifts in solutions of cholesterol and the dipyridine adduct of trisdipivalomethanatoeuropium(III). A shift reagent". Journal of the American Chemical Society. 91 (18): 5160–5162. doi:10.1021/ja01046a038. PMID 5798101.

Ensley, Harry E.; Parnell, Carol A.; Corey, Elias J. (1978). "Convenient synthesis of a highly efficient and recyclable chiral director for asymmetric induction". The Journal of Organic Chemistry. 43 (8): 1610–1612. doi:10.1021/jo00402a037.

Sariaslani, F.Sima; Rosazza, John P.N. (1984). "Biocatalysis in natural products chemistry". Enzyme and Microbial Technology. 6 (6): 242–253. doi:10.1016/0141-0229(84)90125-X.

Wandrey, Christian; Liese, Andreas; Kihumbu, David (2000). "Industrial Biocatalysis: Past, Present, and Future". Organic Process Research & Development. 4 (4): 286–290. doi:10.1021/op990101l.

dx.doi.org

harvard.edu

ui.adsabs.harvard.edu

iupac.org

goldbook.iupac.org

nih.gov

pubmed.ncbi.nlm.nih.gov

Smith, Silas W. (July 2009). "Chiral Toxicology: It's the Same Thing...Only Different". Toxicological Sciences. 110 (1): 4–30. doi:10.1093/toxsci/kfp097. PMID 19414517.

Bauer, Eike B. (2012). "Chiral-at-metal complexes and their catalytic applications in organic synthesis". Chemical Society Reviews. 41 (8): 3153–67. doi:10.1039/C2CS15234G. PMID 22306968.

M. Heitbaum; F. Glorius; I. Escher (2006). "Asymmetric Heterogeneous Catalysis". Angewandte Chemie International Edition. 45 (29): 4732–4762. doi:10.1002/anie.200504212. PMID 16802397.

Bertelsen, Søren; Jørgensen, Karl Anker (2009). "Organocatalysis—after the gold rush". Chemical Society Reviews. 38 (8): 2178–89. doi:10.1039/b903816g. PMID 19623342.

Gal, Joseph (January 2011). "Louis Pasteur, language, and molecular chirality. I. Background and Dissymmetry". Chirality. 23 (1): 1–16. doi:10.1002/chir.20866. PMID 20589938.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

Enantioselective synthesis (English Wikipedia)

acs.org

pubs.acs.org

bnf.fr

gallica.bnf.fr

books.google.com

doi.org

doi.org

dx.doi.org

harvard.edu

ui.adsabs.harvard.edu

hathitrust.org

babel.hathitrust.org

iupac.org

goldbook.iupac.org

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

worldcat.org

search.worldcat.org

zenodo.org