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Asymetrická hydrogenace (Czech Wikipedia)

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

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86doi.org
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64nih.gov
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2harvard.edu
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  • A. Pfaltz. Asymmetric Catalysis Special Feature Part II: Design of chiral ligands for asymmetric catalysis: From C2-symmetric P,P- and N,N-ligands to sterically and electronically nonsymmetrical P,N-ligands. Proceedings of the National Academy of Sciences. 2004, s. 5723–5726. doi:10.1073/pnas.0307152101. PMID 15069193. Bibcode 2004PNAS..101.5723P. 
  • I. D. Gridnev; T. Imamoto. On the Mechanism of Stereoselection in Rh-Catalyzed Asymmetric Hydrogenation: A General Approach for Predicting the Sense of Enantioselectivity. Accounts of Chemical Research. 2004, s. 633–644. doi:10.1021/ar030156e. PMID 15379579. 
  • W. S. Knowles; M. J. Sabacky. Catalytic asymmetric hydrogenation employing a soluble, optically active, rhodium complex. Chemical Communications (London). 1968, s. 1445. doi:10.1039/C19680001445. 
  • C. Pilkington; I. Lennon. The Application of Asymmetric Hydrogenation for the Manufacture of Pharmaceutical Intermediates:The Need for Catalyst Diversity. Synthesis. 2003, s. 1639. doi:10.1055/s-2003-40871. 
  • A. Miyashita; A. Yasuda; H. Takaya; K. Toriumi; T. Ito; T. Souchi; R. Noyori. Synthesis of 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (BINAP), an atropisomeric chiral bis(triaryl)phosphine, and its use in the rhodium(I)-catalyzed asymmetric hydrogenation of α-(acylamino)acrylic acids. Journal of the American Chemical Society. 1980, s. 7932. doi:10.1021/ja00547a020. 
  • R. Noyori; T. Ohkuma; M. Kitamura; H. Takaya; N. Sayo; H. Kumobayashi; S. Akutagawa. Asymmetric hydrogenation of β-keto carboxylic esters. A practical, purely chemical access to β-hydroxy esters in high enantiomeric purity. Journal of the American Chemical Society. 1987, s. 5856. doi:10.1021/ja00253a051. 
  • Takeshi Ohkuma; Christian A. Sandoval; Rajagopal Srinivasan; Lin Quinghong; Wei Yinmao; Kilian Muñiz; Ryoji Noyori. Asymmetric Hydrogenation of tert-Alkyl Ketones. Journal of the American Chemical Society. 2005-06-01, s. 8288–8289. ISSN 0002-7863. doi:10.1021/ja052071. PMID 15941254. 
  • T. Ohkuma; T. Hattori; H. Ooka; T. Inoue; R. Noyori. BINAP/1,4-Diamine−Ruthenium(II) Complexes for Efficient Asymmetric Hydrogenation of 1-Tetralones and Analogues. Organic Letters. 2004, s. 2681–2683. ISSN 0002-7863. doi:10.1021/ol049157c. PMID 15281743. 
  • T. Ikariya; A. J. Blacker. Asymmetric Transfer Hydrogenation of Ketones with Bifunctional Transition Metal-Based Molecular Catalysts. Accounts of Chemical Research. 2007, s. 1300–1308. doi:10.1021/ar700134q. PMID 17960897. 
  • T. L. Church; P. G. Andersson. Iridium catalysts for the asymmetric hydrogenation of olefins with nontraditional functional substituents. Coordination Chemistry Reviews. 2008, s. 513. doi:10.1016/j.ccr.2007.09.015. 
  • A. Lightfoot; P. Schnider; A. Pfaltz. Enantioselective Hydrogenation of Olefins with Iridium-Phosphanodihydrooxazole Catalyst. Angewandte Chemie International Edition. 1998, s. 2897–2899. doi:10.1002/(SICI)1521-3773(19981102)37:20<2897::AID-ANIE2897>3.0.CO;2-8. PMID 29711115. 
  • J. H. Xie; X. Y. Liu; J. B. Xie; L. X. Wang; Q. L. Zhou. An Additional Coordination Group Leads to Extremely Efficient Chiral Iridium Catalysts for Asymmetric Hydrogenation of Ketones. Angewandte Chemie International Edition. 2011, s. 7329–7332. doi:10.1002/anie.201102710. PMID 21751315. 
  • A. Blankenstein, J. R. Blankenstein, R. Hilgraf, E. Hörmann, S. McIntyre, F. Menges, M. Schönleber, S. P. Smidt, B. Wüstenberg, N. Zimmermann. Iridium-Catalyzed Enantioselective Hydrogenation of Olefins. Advanced Synthesis & Catalysis. 2003, s. 33. doi:10.1002/adsc.200390027. 
  • X. Cui; K. Burgess. Catalytic Homogeneous Asymmetric Hydrogenations of Largely Unfunctionalized Alkenes. Chemical Reviews. 2005, s. 3272–3296. doi:10.1021/cr0500131. PMID 16159153. 
  • Y. Xu; D. M. P. Mingos; J. M. Brown. Crabtree's catalyst revisited; Ligand effects on stability and durability. Chemical Communications. 2008, s. 199–201. doi:10.1039/B711979H. PMID 18092086. 
  • Z. J. Wang; G. J. Deng; Y. Li; Y. M. He; W. J. Tang; Q. H. Fan. Enantioselective Hydrogenation of Quinolines Catalyzed by Ir(BINAP)-Cored Dendrimers: Dramatic Enhancement of Catalytic Activity. Organic Letters. 2007, s. 1243–1246. doi:10.1021/ol0631410. PMID 17328554. 
  • S. F. Zhu; J. B. Xie; Y. Z. Zhang; S. Li; Q. L. Zhou. Well-Defined Chiral Spiro Iridium/Phosphine−Oxazoline Cationic Complexes for Highly Enantioselective Hydrogenation of Imines at Ambient Pressure. Journal of the American Chemical Society. 2006, s. 12886–12891. doi:10.1021/ja063444p. PMID 17002383. 
  • H. U. Blaser; B. T. Pugin; F. Spindler; A. Togni. Enantioselective imine hydrogenation with Ir diphosphine catalysts: Fighting deactivation. Comptes Rendus Chimie. 2002, s. 379. doi:10.1016/S1631-0748(02)01391-7. 
  • S. Enthaler; K. Junge; M. Beller. Sustainable Metal Catalysis with Iron: From Rust to a Rising Star?. Angewandte Chemie International Edition. 2008, s. 3317–3321. doi:10.1002/anie.200800012. PMID 18412184. 
  • A. Mikhailine; A. J. Lough; R. H. Morris. Efficient Asymmetric Transfer Hydrogenation of Ketones Catalyzed by an Iron Complex Containing a P−N−N−P Tetradentate Ligand Formed by Template Synthesis. Journal of the American Chemical Society. 2009, s. 1394–1395. doi:10.1021/ja809493h. PMID 19133772. 
  • J. F. Sonnenberg; N. Coombs; P. A. Dube; R. H. Morris. Iron Nanoparticles Catalyzing the Asymmetric Transfer Hydrogenation of Ketones. Journal of the American Chemical Society. 2012, s. 5893–5899. doi:10.1021/ja211658t. PMID 22448656. 
  • J. K. Whitesell. C2 symmetry and asymmetric induction. Chemical Reviews. 1989, s. 1581–1590. doi:10.1021/cr00097a012. 
  • W. S. Knowles; M. J. Sabacky; B. D. Vineyard. Catalytic asymmetric hydrogenation. Journal of the Chemical Society, Chemical Communications. 1972, s. 119–124. doi:10.1039/C39720000010. PMID 4270504. 
  • T. Jerphagnon autor2 = J. L. Renaud; C. Bruneau. Chiral monodentate phosphorus ligands for rhodium-catalyzed asymmetric hydrogenation. Tetrahedron: Asymmetry. 2004, s. 2101. doi:10.1016/j.tetasy.2004.04.037. 
  • M. Van Den Berg; A. J. Minnaard; E. P. Schudde; J. Van Esch; A. H. M. De Vries; J. G. De Vries; B. L. Feringa. Highly Enantioselective Rhodium-Catalyzed Hydrogenation with Monodentate Ligands. Journal of the American Chemical Society. 2000, s. 11539. Dostupné online. doi:10.1021/ja002507f. 
  • Y. Fu; J. H. Xie; A. G. Hu; H. Zhou; L. X. Wang; Q. L. Zhou. Novel monodentate spiro phosphorus ligands for rhodium-catalyzed hydrogenation reactions. Chemical Communications. 2002, s. 480–481. doi:10.1039/B109827F. PMID 12120551. 
  • M. T. Reetz; T. Sell; A. Meiswinkel; G. Mehler. A New Principle in Combinatorial Asymmetric Transition-Metal Catalysis: Mixtures of Chiral Monodentate P Ligands. Angewandte Chemie International Edition. 2003, s. 790–793. doi:10.1002/anie.200390209. PMID 12596201. 
  • B. D. Vineyard; W. S. Knowles; M. J. Sabacky; G. L. Bachman; D. J. Weinkauff. Asymmetric hydrogenation. Rhodium chiral bisphosphine catalyst. Journal of the American Chemical Society. 1977, s. 5946. doi:10.1021/ja00460a018. 
  • W. S. Knowles; M. J. Sabacky; B. D. Vineyard; D. J. Weinkauff. Asymmetric hydrogenation with a complex of rhodium and a chiral bisphosphine. Journal of the American Chemical Society. 1975, s. 2567. doi:10.1021/ja00842a058. 
  • MÜLLER, D.; UMBRICHT, G.; WEBER, B.; PFALTZ, A. C2-Symmetric 4,4',5,5'-Tetrahydrobi(oxazoles) and 4,4',5,5'-Tetrahydro-2,2'-methylenebis[oxazoles] as Chiral Ligands for Enantioselective Catalysis Preliminary Communication. Helvetica Chimica Acta. 1991, s. 232–240. doi:10.1002/hlca.19910740123. 
  • HELMCHEN, G. N.; PFALTZ, A. PhosphinooxazolinesA New Class of Versatile, Modular P,N-Ligands for Asymmetric Catalysis. Accounts of Chemical Research. 2000, s. 336–345. doi:10.1021/ar9900865. PMID 10891051. 
  • FRANZKE, A.; PFALTZ, A. Zwitterionic Iridium Complexes with P,N-Ligands as Catalysts for the Asymmetric Hydrogenation of Alkenes. Chemistry: A European Journal. 2011, s. 4131–44. doi:10.1002/chem.201003314. PMID 21381140. 
  • MAURER, F.; HUCH, V.; ULLRICH, A.; KAZMAIER, U. Development of Catalysts for the Stereoselective Hydrogenation of α,β-Unsaturated Ketones. The Journal of Organic Chemistry. 2012, s. 5139–5143. doi:10.1021/jo300246c. PMID 22571628. 
  • RAGEOT, D.; WOODMANSEE, D. H.; PUGIN, B. T.; PFALTZ, A. Proline-Based P,O Ligand/Iridium Complexes as Highly Selective Catalysts: Asymmetric Hydrogenation of Trisubstituted Alkenes. Angewandte Chemie International Edition. 2011, s. 9598–601. doi:10.1002/anie.201104105. PMID 21882320. 
  • PERRY, M. C.; CUI, X.; POWELL, M. T.; HOU, D. R.; REIBENSPIES, J. H.; BURGESS, K. Optically Active Iridium Imidazol-2-ylidene-oxazoline Complexes: Preparation and Use in Asymmetric Hydrogenation of Arylalkenes. Journal of the American Chemical Society. 2003, s. 113–123. doi:10.1021/ja028142b. PMID 12515512. 
  • NANCHEN, S.; PFALTZ, A. Synthesis and Application of Chiral N-Heterocyclic Carbene–Oxazoline Ligands: Iridium-Catalyzed Enantioselective Hydrogenation. Chemistry: A European Journal. 2006, s. 4550–8. doi:10.1002/chem.200501500. PMID 16557626. 
  • ZHU, Y.; BURGESS, K. Iridium-Catalyzed Asymmetric Hydrogenation of Vinyl Ethers. Advanced Synthesis & Catalysis. 2008, s. 979. doi:10.1002/adsc.200700546. 
  • ZHAO, J.; BURGESS, K. Aldol-Type Chirons from Asymmetric Hydrogenations of Trisubstituted Alkenes. Organic Letters. 2009, s. 2053–2056. doi:10.1021/ol900308w. PMID 19368378. 
  • ZHAO, J.; BURGESS, K. Synthesis of Vicinal Dimethyl Chirons by Asymmetric Hydrogenation of Trisubstituted Alkenes. Journal of the American Chemical Society. 2009, s. 13236–13237. doi:10.1021/ja905458n. PMID 19719102. 
  • ZHOU, J.; BURGESS, K. Α,ω-Functionalized 2,4-Dimethylpentane Dyads and 2,4,6-Trimethylheptane Triads through Asymmetric Hydrogenation. Angewandte Chemie International Edition. 2007, s. 1129–31. doi:10.1002/anie.200603635. PMID 17200966. 
  • ZHOU, J.; ZHU, Y.; BURGESS, K. Synthesis of (S,R,R,S,R,S)-4,6,8,10,16,18- Hexamethyldocosane from Antitrogus parvulus via Diastereoselective Hydrogenations. Organic Letters. 2007, s. 1391–1393. doi:10.1021/ol070298z. PMID 17338543. 
  • URBAN, S.; ORTEGA, N.; GLORIUS, F. Ligand-Controlled Highly Regioselective and Asymmetric Hydrogenation of Quinoxalines Catalyzed by Ruthenium N-Heterocyclic Carbene Complexes. Angewandte Chemie International Edition. 2011, s. 3803–6. doi:10.1002/anie.201100008. PMID 21442699. 
  • PÀMIES, O.; ANDERSSON, P. G.; DIÉGUEZ, M. Asymmetric Hydrogenation of Minimally Functionalised Terminal Olefins: An Alternative Sustainable and Direct Strategy for Preparing Enantioenriched Hydrocarbons. Chemistry: A European Journal. 2010, s. 14232–40. doi:10.1002/chem.201001909. PMID 21140401. 
  • WOODMANSEE, D. H.; PFALTZ, A. Asymmetric hydrogenation of alkenes lacking coordinating groups. Chemical Communications. 2011, s. 7912–7916. doi:10.1039/c1cc11430a. PMID 21556431. 
  • MAZUELA, J.; VERENDEL, J. J.; COLL, M.; SCHÄFFNER, B. N.; BÖRNER, A.; ANDERSSON, P. G.; PÀMIES, O. Iridium Phosphite−Oxazoline Catalysts for the Highly Enantioselective Hydrogenation of Terminal Alkenes. Journal of the American Chemical Society. 2009, s. 12344–12353. doi:10.1021/ja904152r. PMID 19658416. 
  • HOU, G. H.; XIE, J. H.; WANG, L. X.; ZHOU, Q. L. Highly Efficient Rh(I)-Catalyzed Asymmetric Hydrogenation of Enamines Using Monodente Spiro Phosphonite Ligands. Journal of the American Chemical Society. 2006, s. 11774–11775. doi:10.1021/ja0644778. PMID 16953614. 
  • HOU, G. H.; XIE, J. H.; YAN, P. C.; ZHOU, Q. L. Iridium-Catalyzed Asymmetric Hydrogenation of Cyclic Enamines. Journal of the American Chemical Society. 2009, s. 1366–1367. doi:10.1021/ja808358r. PMID 19132836. 
  • OHKUMA, T.; OOKA, H.; HASHIGUCHI, S.; IKARIYA, T.; NOYORI, R. Practical Enantioselective Hydrogenation of Aromatic Ketones. Journal of the American Chemical Society. 1995, s. 2675. doi:10.1021/ja00114a043. 
  • NOYORI, R.; OHKUMA, T. Asymmetric Catalysis by Architectural and Functional Molecular Engineering: Practical Chemo- and Stereoselective Hydrogenation of Ketones. Angewandte Chemie International Edition. 2001, s. 40–73. doi:10.1002/1521-3773(20010105)40:1<40::AID-ANIE40>3.0.CO;2-5. PMID 11169691. 
  • HEMS, W. P.; GROARKE, M.; ZANOTTI-GEROSA, A.; GRASA, G. A. [(Bisphosphine) Ru(II) Diamine] Complexes in Asymmetric Hydrogenation: Expanding the Scope of the Diamine Ligand. Accounts of Chemical Research. 2007, s. 1340–1347. doi:10.1021/ar7000233. PMID 17576143. 
  • NOYORI, R.; YAMAKAWA, M.; HASHIGUCHI, S. Metal−Ligand Bifunctional Catalysis: A Nonclassical Mechanism for Asymmetric Hydrogen Transfer between Alcohols and Carbonyl Compounds. The Journal of Organic Chemistry. 2001, s. 7931–7944. doi:10.1021/jo010721w. PMID 11722188. 
  • YU, Z.; JIN, W.; JIANG, Q. Brønsted Acid Activation Strategy in Transition-Metal Catalyzed Asymmetric Hydrogenation of N-Unprotected Imines, Enamines, and N-Heteroaromatic Compounds. Angewandte Chemie International Edition. 2012, s. 6060–72. doi:10.1002/anie.201200963. PMID 22577004. 
  • HOU, G.; GOSSELIN, F.; LI, W.; MCWILLIAMS, J. C.; SUN, Y.; WEISEL, M.; O'SHEA, P. D. Enantioselective Hydrogenation of N−H Imines. Journal of the American Chemical Society. 2009, s. 9882–9883. doi:10.1021/ja903319r. PMID 19569686. 
  • HOU, G.; TAO, R.; SUN, Y.; ZHANG, X.; GOSSELIN, F. Iridium−Monodentate Phosphoramidite-Catalyzed Asymmetric Hydrogenation of Substituted Benzophenone N−H Imines. Journal of the American Chemical Society. 2010, s. 2124–2125. doi:10.1021/ja909583s. PMID 20104899. 
  • ZHOU, Y. G. Asymmetric Hydrogenation of Heteroaromatic Compounds. Accounts of Chemical Research. 2007, s. 1357–1366. doi:10.1021/ar700094b. PMID 17896823. 
  • WANG, W. B.; LU, S. M.; YANG, P. Y.; HAN, X. W.; ZHOU, Y. G. Highly Enantioselective Iridium-Catalyzed Hydrogenation of Heteroaromatic Compounds, Quinolines. Journal of the American Chemical Society. 2003, s. 10536–10537. doi:10.1021/ja0353762. PMID 12940733. 
  • XU, L.; LAM, K. H.; JI, J.; WU, J.; FAN, Q. H.; LO, W. H.; CHAN, A. S. C. Air-stable Ir-(P-Phos) complex for highly enantioselective hydrogenation of quinolines and their immobilization in poly(ethylene glycol) dimethyl ether (DMPEG). Chemical Communications. 2005, s. 1390–2. doi:10.1039/B416397D. PMID 15756313. 
  • LAM, K. H.; XU, L.; FENG, L.; FAN, Q. H.; LAM, F. L.; LO, W. H.; CHAN, A. S. C. Highly Enantioselective Iridium-Catalyzed Hydrogenation of Quinoline Derivatives Using Chiral Phosphinite H8-BINAPO. Advanced Synthesis & Catalysis. 2005, s. 1755. doi:10.1002/adsc.200505130. 
  • QIU, L.; KWONG, F. Y.; WU, J.; LAM, W. H.; CHAN, S.; YU, W. Y.; LI, Y. M. A New Class of Versatile Chiral-Bridged Atropisomeric Diphosphine Ligands: Remarkably Efficient Ligand Syntheses and Their Applications in Highly Enantioselective Hydrogenation Reactions. Journal of the American Chemical Society. 2006, s. 5955–5965. doi:10.1021/ja0602694. PMID 16637664. 
  • Rueping; ANTONCHICK, A.; THEISSMANN, T. A highly enantioselective Brønsted acid catalyzed cascade reaction: organocatalytic transfer hydrogenation of quinolines and their application in the synthesis of alkaloids. Angewandte Chemie International Edition in English. 2006, s. 3683–3686. doi:10.1002/anie.200600191. PMID 16639754. 
  • TANG, W.; XU, L.; FAN, Q. H.; WANG, J.; FAN, B.; ZHOU, Z.; LAM, K. H. Asymmetric Hydrogenation of Quinoxalines with Diphosphinite Ligands: A Practical Synthesis of Enantioenriched, Substituted Tetrahydroquinoxalines. Angewandte Chemie International Edition. 2009, s. 9135–9138. doi:10.1002/anie.200904518. PMID 19876991. 
  • RUEPING, M.; TATO, F.; SCHOEPKE, F. R. The First General, Efficient and Highly Enantioselective Reduction of Quinoxalines and Quinoxalinones. Chemistry: A European Journal. 2010, s. 2688–91. doi:10.1002/chem.200902907. PMID 20140920. 
  • GLORIUS, F.; SPIELKAMP, N.; HOLLE, S.; GODDARD, R.; LEHMANN, C. W. Efficient Asymmetric Hydrogenation of Pyridines. Angewandte Chemie International Edition. 2004, s. 2850–2. doi:10.1002/anie.200453942. PMID 15150766. 
  • YE, Z. S.; CHEN, M. W.; CHEN, Q. A.; SHI, L.; DUAN, Y.; ZHOU, Y. G. Iridium-Catalyzed Asymmetric Hydrogenation of Pyridinium Salts. Angewandte Chemie International Edition. 2012, s. 10181–4. doi:10.1002/anie.201205187. PMID 22969060. 
  • TANG, W. J.; TAN, J.; XU, L. J.; LAM, K. H.; FAN, Q. H.; CHAN, A. S. C. Highly Enantioselective Hydrogenation of Quinoline and Pyridine Derivatives with Iridium-(P-Phos) Catalyst. Advanced Synthesis & Catalysis. 2010, s. 1055. doi:10.1002/adsc.200900870. 
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  • KUWANO, R.; SATO, K.; KUROKAWA, T.; KARUBE, D.; ITO, Y. Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles. Journal of the American Chemical Society. 2000, s. 7614. doi:10.1021/ja001271c. 
  • KUWANO, R.; KANEDA, K.; ITO, T.; SATO, K.; KUROKAWA, T.; ITO, Y. Highly Enantioselective Synthesis of Chiral 3-Substituted Indolines by Catalytic Asymmetric Hydrogenation of Indoles. Organic Letters. 2004, s. 2213–2215. doi:10.1021/ol049317k. PMID 15200323. 
  • KUWANO, R.; KASHIWABARA, M.; SATO, K.; ITO, T.; KANEDA, K.; ITO, Y. Catalytic asymmetric hydrogenation of indoles using a rhodium complex with a chiral bisphosphine ligand PhTRAP. Tetrahedron: Asymmetry. 2006, s. 521. doi:10.1016/j.tetasy.2006.01.016. 
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  • XIAO, Y. C.; WANG, C.; YAO, Y.; SUN, J.; CHEN, Y. C. Direct Asymmetric Hydrosilylation of Indoles: Combined Lewis Base and Brønsted Acid Activation. Angewandte Chemie International Edition. 2011, s. 10661–4. doi:10.1002/anie.201105341. PMID 21932274. 
  • DUAN, Y.; CHEN, M. W.; YE, Z. S.; WANG, D. S.; CHEN, Q. A.; ZHOU, Y. G. An Enantioselective Approach to 2,3-Disubstituted Indolines through Consecutive Brønsted Acid/Pd-Complex-Promoted Tandem Reactions. Chemistry: A European Journal. 2011, s. 7193–7. doi:10.1002/chem.201100576. PMID 21567504. 
  • KUWANO, R.; KASHIWABARA, M.; OHSUMI, M.; KUSANO, H. Catalytic Asymmetric Hydrogenation of 2,3,5-Trisubstituted Pyrroles. Journal of the American Chemical Society. 2008, s. 808–809. doi:10.1021/ja7102422. PMID 18154340. 
  • WANG, D. S.; YE, Z. S.; CHEN, Q. A.; ZHOU, Y. G.; YU, C. B.; FAN, H. J.; DUAN, Y. Highly Enantioselective Partial Hydrogenation of Simple Pyrroles: A Facile Access to Chiral 1-Pyrrolines. Journal of the American Chemical Society. 2011, s. 8866–8869. doi:10.1021/ja203190t. PMID 21591641. 
  • WANG, D. S.; CHEN, Q. A.; LU, S. M.; ZHOU, Y. G. Asymmetric Hydrogenation of Heteroarenes and Arenes. Chemical Reviews. 2012, s. 2557–2590. doi:10.1021/cr200328h. PMID 22098109. 
  • ORTEGA, Nuria; URBAN, Slawomir; BEIRING, Bernhard; GLORIUS, Frank. Ruthenium NHC Catalyzed Highly Asymmetric Hydrogenation of Benzofurans. Angewandte Chemie International Edition. 2012, s. 1710–3. doi:10.1002/anie.201107811. PMID 22311814. 
  • WYSOCKI, Jędrzej; ORTEGA, Nuria; GLORIUS, Frank. Asymmetric Hydrogenation of Disubstituted Furans. Angewandte Chemie International Edition. 2014, s. 8751–5. doi:10.1002/anie.201310985. PMID 24554623. 
  • URBAN, S.; BEIRING, B.; ORTEGA, N.; PAUL, D.; GLORIUS, F. Asymmetric Hydrogenation of Thiophenes and Benzothiophenes. Journal of the American Chemical Society. 2012, s. 15241–15244. doi:10.1021/ja306622y. PMID 22934527. 
  • HEITBAUM, M.; GLORIUS, F.; ESCHER, I. Asymmetric Heterogeneous Catalysis. Angewandte Chemie International Edition. 2006, s. 4732–62. doi:10.1002/anie.200504212. PMID 16802397. 
  • BLASER, H. U.; SPINDLER, F.; STUDER, M. Enantioselective catalysis in fine chemicals production. Applied Catalysis A: General. 2001, s. 119–143. doi:10.1016/S0926-860X(01)00801-8. PMID 12613584. 
  • DUB, Pavel A.; GORDON, John C. The role of the metal-bound N–H functionality in Noyori-type molecular catalysts. Nature Reviews Chemistry. 2018, s. 396–408. doi:10.1038/s41570-018-0049-z. 
  • Asymmetric Catalysis on Industrial Scale. Redakce Blaser Hans-Ulrich. Weinheim: Wiley-VCH, 2010. ISBN 978-3-527-63063-9. doi:10.1002/9783527630639. S. 13–16. 

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