Coreyova–Itsunova redukce (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Coreyova–Itsunova redukce" in Czech language version.

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20doi.org

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5nih.gov

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1harvard.edu

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1archive.org

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archive.org (Global: 6^th place; Czech: 10^th place)

Michael Bulliard. Handbook of Chiral Chemicals. Příprava vydání David Ager. [s.l.]: Marcel Decker, 1999. Dostupné online. ISBN 0824710584. Kapitola Chapter 11.1: Asymmetric Reduction of Prochiral Ketones Catalyzed by Oxazaborolidines, s. 211–225.

doi.org (Global: 2^nd place; Czech: 4^th place)

A. Hirao; S. Itsuno; S. Nakahama; N. Yamazaki. Asymmetric reduction of aromatic ketones with chiral alkoxy-amineborane complexes. Journal of the Chemical Society, Chemical Communications. S. 315. doi:10.1039/C39810000315.
E. J. Corey; R. K. Bakshi; S. Shibata. Highly enantioselective borane reduction of ketones catalyzed by chiral oxazaborolidines. Mechanism and synthetic implications. Journal of the American Chemical Society. 1987, s. 5551–5553. doi:10.1021/ja00252a056.
E. J. Corey; R. K. Bakshi; S. Shibata; C. P. Chen; V. K. Singh. A stable and easily prepared catalyst for the enantioselective reduction of ketones. Applications to multistep syntheses. Journal of the American Chemical Society. 1987, s. 7925–7926. doi:10.1021/ja00259a075.
L. Deloux; M. Srebnik. Asymmetric boron-catalyzed reactions. Chemical Reviews. 1993, s. 763–784. doi:10.1021/cr00018a007.
E. J. Corey; C. J. Helal. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method. Angewandte Chemie International Edition. 1998, s. 1986–2012. doi:10.1002/(sici)1521-3773(19980817)37:15<1986::aid-anie1986>3.0.co;2-z. PMID 29711061.
B. T. Cho. Recent advances in the synthetic applications of the oxazaborolidine-mediated asymmetric reduction. Tetrahedron. 2006, s. 7621–7643. doi:10.1016/j.tet.2006.05.036.
Corey, E. J.; AZIMIOARA, M.; SARSHAR, S. X-Ray crystal structure of a chiral oxazaborolidine catalyst for enantioselective carbonyl reduction. Tetrahedron Letters. 1992, s. 3429–3430. doi:10.1016/s0040-4039(00)92654-6.
D. Evans. Stereoselective organic reactions: catalysts for carbonyl addition processes. Science. 1988, s. 420–426. doi:10.1126/science.3358127. PMID 3358127. Bibcode 1988Sci...240..420E.
D. K. Jones; D. C. Liotta; I. Shinkai; D. J. Mathre. Origins of the enantioselectivity observed in oxazaborolidine-catalyzed reductions of ketones. The Journal of Organic Chemistry. 1993, s. 799–801. doi:10.1021/jo00056a001.
E. J. Corey. New enantioselective routes to biologically interesting compounds. Journal of the American Chemical Society. 1990, s. 1209–1216. doi:10.1351/pac199062071209.
V. Nevalainen. Quantum chemical modeling of chiral catalysis. Part 15. On the role of hydride-bridged borane - alkoxyborane complexes in the catalytic enantioselective reduction of ketones promoted by chiral oxazaborolidines. Tetrahedron: Asymmetry. 1994, s. 289–296. doi:10.1016/s0957-4166(00)86186-8.
G. J. Quallich; J. F. Blake; T. M. Woodall. A combined synthetic and ab initio study of chiral oxazaborolidines structure and enantioselectivity relationships. Journal of the American Chemical Society. 1994, s. 8516–8525. doi:10.1021/ja00098a012.
G. J. Quallich; T. M. Woodall. Enantioselective oxazaborolidine reduction of ketones containing heteroatoms. Tetrahedron Letters. 1993, s. 785–788. doi:10.1016/0040-4039(93)89012-f.
Jones, T. K.; MOHAN, J. J.; XAVIER, L. C.; BLACKLOCK, T. J.; MATHRE, D. J.; SOHAR, P.; JONES, E. T. T. An asymmetric synthesis of MK-0417. Observations on oxazaborolidine-catalyzed reductions. The Journal of Organic Chemistry. 1991, s. 763–769. doi:10.1021/jo00002a050.
E. J. Corey; J. O. Link. A new chiral catalyst for the enantioselective synthesis of secondary alcohols and deuterated primary alcohols by carbonyl reduction. Tetrahedron Letters. 1989, s. 6275–6278. doi:10.1016/s0040-4039(01)93871-7.
E. J. Corey; R. K. Bakshi. A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids. Tetrahedron Letters. 1990, s. 611–614. doi:10.1016/s0040-4039(00)94581-7.
S. M. Nettles; K. Matos; E. R. Burkhardt; D. R. Rouda; J. A. Corella. Role of NaBH 4 Stabilizer in the Oxazaborolidine-Catalyzed Asymmetric Reduction of Ketones with BH 3 - THF. The Journal of Organic Chemistry. 2002, s. 2970–2976. doi:10.1021/jo016257c. PMID 11975554.
Rajendra D. Mahale; Sudhir P. Chaskar; Kiran E. Patil; Golak C. Maikap; Mukund K. Gurjar. Corey–Itsuno Reduction of Ketones: A Development of Safe and Inexpensive Process for Synthesis of Some API Intermediates. Organic Process Research & Development. 2012, s. 710–713. doi:10.1021/op300034u. PMID 11975554.
R. T. Stemmler. CBS Oxazaborolidines - Versatile Catalysts for Asymmetric Synthesis. Synlett. 2007, s. 0997–0998. doi:10.1055/s-2007-973876.
D. Prabhakar Reddy; Ning Zhang; Zhimei Yu; Zhen Wang; Yun He. Total Synthesis of Kanamienamide. The Journal of Organic Chemistry. 2017-10-02, s. 11262–11268. ISSN 0022-3263. doi:10.1021/acs.joc.7b01984. PMID 28944669.

harvard.edu (Global: 18^th place; Czech: 99^th place)

adsabs.harvard.edu

D. Evans. Stereoselective organic reactions: catalysts for carbonyl addition processes. Science. 1988, s. 420–426. doi:10.1126/science.3358127. PMID 3358127. Bibcode 1988Sci...240..420E.

nih.gov (Global: 4^th place; Czech: 8^th place)

ncbi.nlm.nih.gov

E. J. Corey; C. J. Helal. Reduction of Carbonyl Compounds with Chiral Oxazaborolidine Catalysts: A New Paradigm for Enantioselective Catalysis and a Powerful New Synthetic Method. Angewandte Chemie International Edition. 1998, s. 1986–2012. doi:10.1002/(sici)1521-3773(19980817)37:15<1986::aid-anie1986>3.0.co;2-z. PMID 29711061.
D. Evans. Stereoselective organic reactions: catalysts for carbonyl addition processes. Science. 1988, s. 420–426. doi:10.1126/science.3358127. PMID 3358127. Bibcode 1988Sci...240..420E.
S. M. Nettles; K. Matos; E. R. Burkhardt; D. R. Rouda; J. A. Corella. Role of NaBH 4 Stabilizer in the Oxazaborolidine-Catalyzed Asymmetric Reduction of Ketones with BH 3 - THF. The Journal of Organic Chemistry. 2002, s. 2970–2976. doi:10.1021/jo016257c. PMID 11975554.
Rajendra D. Mahale; Sudhir P. Chaskar; Kiran E. Patil; Golak C. Maikap; Mukund K. Gurjar. Corey–Itsuno Reduction of Ketones: A Development of Safe and Inexpensive Process for Synthesis of Some API Intermediates. Organic Process Research & Development. 2012, s. 710–713. doi:10.1021/op300034u. PMID 11975554.
D. Prabhakar Reddy; Ning Zhang; Zhimei Yu; Zhen Wang; Yun He. Total Synthesis of Kanamienamide. The Journal of Organic Chemistry. 2017-10-02, s. 11262–11268. ISSN 0022-3263. doi:10.1021/acs.joc.7b01984. PMID 28944669.

worldcat.org (Global: 5^th place; Czech: 3^rd place)

D. Prabhakar Reddy; Ning Zhang; Zhimei Yu; Zhen Wang; Yun He. Total Synthesis of Kanamienamide. The Journal of Organic Chemistry. 2017-10-02, s. 11262–11268. ISSN 0022-3263. doi:10.1021/acs.joc.7b01984. PMID 28944669.

Coreyova–Itsunova redukce (Czech Wikipedia)

archive.org (Global: 6th place; Czech: 10th place)

doi.org (Global: 2nd place; Czech: 4th place)

harvard.edu (Global: 18th place; Czech: 99th place)