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硫脲有机催化 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "硫脲有机催化" in Chinese language version.

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22doi.org
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19worldcat.org
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13nih.gov
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2web.archive.org
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2archive.org
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2figshare.com
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1wiley.com
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1uni-giessen.de
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doi.org

  • Alexander Wittkopp, Peter R. Schreiner, "Diels-Alder Reactions in Water and in Hydrogen-Bonding Environments", book chapter in "The Chemistry of Dienes and Polyenes" Zvi Rappoport (Ed.), Volume 2, John Wiley & Sons Inc.; Chichester, 2000, 1029-1088. ISBN 0-471-72054-2.

    Alexander Wittkopp, "Organocatalysis of Diels-Alder Reactions by Neutral Hydrogen Bond Donors in Organic and Aqueous Solvents", dissertation written in German, Universität Göttingen, 2001. English abstract/download:

    Peter R. Schreiner, review: "Metal-free organocatalysis through explicit hydrogen bonding interactions", Chem. Soc. Rev. 2003, 32, 289-296. abstract/download:

    M. Kotke and P. R. Schreiner. Acid-free, organocatalytic acetalization. Tetrahedron. 2006, 62 (2–3): 434–439. doi:10.1016/j.tet.2005.09.079. M. P. Petri. Activation of Carbonyl Compounds by Double Hydrogen Bonding: An Emerging Tool in Asymmetric Catalysis. Angewandte Chemie International Edition. 2004, 43 (16): 2062–2064. PMID 15083451. doi:10.1002/anie.200301732. 

    Yoshiji Takemoto, review: "Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogen-bonding donors", Org. Biomol. Chem. 2005, 3, 4299-4306. abstract/download: Mark S. Taylor, Eric N. Jacobsen. Asymmetric Catalysis by Chiral Hydrogen-Bond Donors. Angewandte Chemie International Edition. 2006, 45 (10): 1520–1543. PMID 16491487. doi:10.1002/anie.200503132. J. C. Stephen. Organocatalysis Mediated by (Thio)urea Derivatives. Chemistry: A European Journal. 2006, 12 (21): 5418–5427. PMID 16514689. doi:10.1002/chem.200501076. 
  • Kotke, Mike; Peter Schreiner. Generally Applicable Organocatalytic Tetrahydropyranylation of Hydroxy Functionalities with Very Low Catalyst Loading. Synthesis. 2007, 2007 (5): 779–790. ISSN 0039-7881. doi:10.1055/s-2007-965917. 
  • Schreiner, Peter R.; Alexander Wittkopp. H-Bonding Additives Act Like Lewis Acid Catalysts. Organic Letters. 2002, 4 (2): 217–220. ISSN 1523-7060. PMID 11796054. doi:10.1021/ol017117s. 
  • Chauhan, P.; Mahajan, S.; Kaya, U.; Hack, D.; Enders, D. Bifunctional Amine-Squaramides: Powerful Hydrogen-Bonding Organocatalysts for Asymmetric Domino/Cascade Reactions. Adv. Synth. Catal. 2015, 357 (2–3): 253–281. doi:10.1002/adsc.201401003. 
  • Wittkopp, Alexander; Peter R. Schreiner. Metal-Free, Noncovalent Catalysis of Diels–Alder Reactions by Neutral Hydrogen Bond Donors in Organic Solvents and in Water. Chemistry: A European Journal. 2003, 9 (2): 407–414. ISSN 0947-6539. PMID 12532289. doi:10.1002/chem.200390042. 
  • Bordwell, Frederick G.; Ji, Guo Zhen. Effects of structural changes on acidities and homolytic bond dissociation energies of the hydrogen-nitrogen bonds in amidines, carboxamides, and thiocarboxamides. Journal of the American Chemical Society. 1991-10-01, 113 (22): 8398–8401. ISSN 0002-7863. doi:10.1021/ja00022a029. 
  • A. Wittkopp and P. R. Schreiner. Metal-Free, Noncovalent Catalysis of Diels-Alder Reactions by Neutral Hydrogen Bond Donors in Organic Solvents and in Water. Chemistry: A European Journal. 2003, 9 (2): 407–414. PMID 12532289. doi:10.1002/chem.200390042. 
  • Sigman, Matthew S.; Eric N. Jacobsen. Schiff Base Catalysts for the Asymmetric Strecker Reaction Identified and Optimized from Parallel Synthetic Libraries. Journal of the American Chemical Society. 1998, 120 (19): 4901–4902. ISSN 0002-7863. doi:10.1021/ja980139y. 
  • Sigman, Matthew S.; Petr Vachal; Eric N. Jacobsen. A General Catalyst for the Asymmetric Strecker Reaction. Angewandte Chemie International Edition. 2000, 39 (7): 1279–1281. ISSN 1433-7851. PMID 10767031. doi:10.1002/(SICI)1521-3773(20000403)39:7<1279::AID-ANIE1279>3.0.CO;2-U. 
  • Okino, Tomotaka; Yasutaka Hoashi; Yoshiji Takemoto. Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts. Journal of the American Chemical Society. 2003, 125 (42): 12672–12673. ISSN 0002-7863. PMID 14558791. doi:10.1021/ja036972z. 
  • Sohtome, Yoshihiro; Aya Tanatani; Yuichi Hashimoto; Kazuo Nagasawa. Development of bis-thiourea-type organocatalyst for asymmetric Baylis–Hillman reaction☆. Tetrahedron Letters. 2004, 45 (29): 5589–5592. ISSN 0040-4039. doi:10.1016/j.tetlet.2004.05.137. 
  • Sohtome, Yoshihiro; Yuichi Hashimoto; Kazuo Nagasawa. Guanidine-Thiourea Bifunctional Organocatalyst for the Asymmetric Henry (Nitroaldol) Reaction. Advanced Synthesis & Catalysis. 2005, 347 (11–13): 1643–1648. ISSN 1615-4150. doi:10.1002/adsc.200505148. 
  • Herrera, Raquel P.; Valentina Sgarzani; Luca Bernardi; Alfredo Ricci. Catalytic Enantioselective Friedel-Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst. Angewandte Chemie International Edition. 2005, 44 (40): 6576–6579. ISSN 1433-7851. PMID 16172992. doi:10.1002/anie.200500227. 
  • Wang, Jian; Hao Li; Xinhong Yu; Liansuo Zu; Wei Wang. Chiral Binaphthyl-Derived Amine-Thiourea Organocatalyst-Promoted Asymmetric Morita−Baylis−Hillman Reaction. Organic Letters. 2005, 7 (19): 4293–4296. ISSN 1523-7060. PMID 16146410. doi:10.1021/ol051822+. 
  • Vakulya, Benedek; Szilárd Varga; Antal Csámpai; Tibor Soós. Highly Enantioselective Conjugate Addition of Nitromethane to Chalcones Using Bifunctional Cinchona Organocatalysts. Organic Letters. 2005, 7 (10): 1967–1969. ISSN 1523-7060. PMID 15876031. doi:10.1021/ol050431s. 
  • McCooey, Séamus H.; Stephen J. Connon. Urea- and Thiourea-Substituted Cinchona Alkaloid Derivatives as Highly Efficient Bifunctional Organocatalysts for the Asymmetric Addition of Malonate to Nitroalkenes: Inversion of Configuration at C9 Dramatically Improves Catalyst Performance. Angewandte Chemie International Edition. 2005, 44 (39): 6367–6370. ISSN 1433-7851. PMID 16136619. doi:10.1002/anie.200501721. 
  • Cao, Chun-Li; Meng-Chun Ye; Xiu-Li Sun; Yong Tang. Pyrrolidine−Thiourea as a Bifunctional Organocatalyst: Highly Enantioselective Michael Addition of Cyclohexanone to Nitroolefins. Organic Letters. 2006, 8 (14): 2901–2904. ISSN 1523-7060. PMID 16805512. doi:10.1021/ol060481c. 
  • Miyabe, Hideto; Sayo Tuchida; Masashige Yamauchi; Yoshiji Takemoto. Reaction of Nitroorganic Compounds Using Thiourea Catalysts Anchored to Polymer Support. Synthesis. 2006, 2006 (19): 3295–3300. ISSN 0039-7881. doi:10.1055/s-2006-950196. 
  • Wanka, Lukas; Chiara Cabrele; Maksims Vanejews; Peter R. Schreiner. γ-Aminoadamantanecarboxylic Acids Through Direct C–H Bond Amidations. European Journal of Organic Chemistry. 2007, 2007 (9): 1474–1490. ISSN 1434-193X. doi:10.1002/ejoc.200600975. 
  • Yamaoka, Yousuke; Hideto Miyabe; Yoshiji Takemoto. Catalytic Enantioselective Petasis-Type Reaction of Quinolines Catalyzed by a Newly Designed Thiourea Catalyst. Journal of the American Chemical Society. 2007, 129 (21): 6686–6687. ISSN 0002-7863. PMID 17488015. doi:10.1021/ja071470x. 
  • Liu, Kun; Han-Feng Cui; Jing Nie; Ke-Yan Dong; Xiao-Juan Li; Jun-An Ma. Highly Enantioselective Michael Addition of Aromatic Ketones to Nitroolefins Promoted by Chiral Bifunctional Primary Amine-thiourea Catalysts Based on Saccharides. Organic Letters. 2007, 9 (5): 923–925. ISSN 1523-7060. PMID 17288432. doi:10.1021/ol0701666. 
  • Li, Xiao-Juan; Kun Liu; Hai Ma; Jing Nie; Jun-An Ma. Highly Enantioselective Michael Addition of Malonates to Nitroolefins Catalyzed by Chiral Bifunctional Tertiary Amine-Thioureas Based on Saccharides. Synlett. 2008, 2008 (20): 3242–3246. ISSN 0936-5214. doi:10.1055/s-0028-1087370. 

figshare.com

nih.gov

ncbi.nlm.nih.gov

  • Alexander Wittkopp, Peter R. Schreiner, "Diels-Alder Reactions in Water and in Hydrogen-Bonding Environments", book chapter in "The Chemistry of Dienes and Polyenes" Zvi Rappoport (Ed.), Volume 2, John Wiley & Sons Inc.; Chichester, 2000, 1029-1088. ISBN 0-471-72054-2.

    Alexander Wittkopp, "Organocatalysis of Diels-Alder Reactions by Neutral Hydrogen Bond Donors in Organic and Aqueous Solvents", dissertation written in German, Universität Göttingen, 2001. English abstract/download:

    Peter R. Schreiner, review: "Metal-free organocatalysis through explicit hydrogen bonding interactions", Chem. Soc. Rev. 2003, 32, 289-296. abstract/download:

    M. Kotke and P. R. Schreiner. Acid-free, organocatalytic acetalization. Tetrahedron. 2006, 62 (2–3): 434–439. doi:10.1016/j.tet.2005.09.079. M. P. Petri. Activation of Carbonyl Compounds by Double Hydrogen Bonding: An Emerging Tool in Asymmetric Catalysis. Angewandte Chemie International Edition. 2004, 43 (16): 2062–2064. PMID 15083451. doi:10.1002/anie.200301732. 

    Yoshiji Takemoto, review: "Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogen-bonding donors", Org. Biomol. Chem. 2005, 3, 4299-4306. abstract/download: Mark S. Taylor, Eric N. Jacobsen. Asymmetric Catalysis by Chiral Hydrogen-Bond Donors. Angewandte Chemie International Edition. 2006, 45 (10): 1520–1543. PMID 16491487. doi:10.1002/anie.200503132. J. C. Stephen. Organocatalysis Mediated by (Thio)urea Derivatives. Chemistry: A European Journal. 2006, 12 (21): 5418–5427. PMID 16514689. doi:10.1002/chem.200501076. 
  • Schreiner, Peter R.; Alexander Wittkopp. H-Bonding Additives Act Like Lewis Acid Catalysts. Organic Letters. 2002, 4 (2): 217–220. ISSN 1523-7060. PMID 11796054. doi:10.1021/ol017117s. 
  • Wittkopp, Alexander; Peter R. Schreiner. Metal-Free, Noncovalent Catalysis of Diels–Alder Reactions by Neutral Hydrogen Bond Donors in Organic Solvents and in Water. Chemistry: A European Journal. 2003, 9 (2): 407–414. ISSN 0947-6539. PMID 12532289. doi:10.1002/chem.200390042. 
  • A. Wittkopp and P. R. Schreiner. Metal-Free, Noncovalent Catalysis of Diels-Alder Reactions by Neutral Hydrogen Bond Donors in Organic Solvents and in Water. Chemistry: A European Journal. 2003, 9 (2): 407–414. PMID 12532289. doi:10.1002/chem.200390042. 
  • Sigman, Matthew S.; Petr Vachal; Eric N. Jacobsen. A General Catalyst for the Asymmetric Strecker Reaction. Angewandte Chemie International Edition. 2000, 39 (7): 1279–1281. ISSN 1433-7851. PMID 10767031. doi:10.1002/(SICI)1521-3773(20000403)39:7<1279::AID-ANIE1279>3.0.CO;2-U. 
  • Okino, Tomotaka; Yasutaka Hoashi; Yoshiji Takemoto. Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts. Journal of the American Chemical Society. 2003, 125 (42): 12672–12673. ISSN 0002-7863. PMID 14558791. doi:10.1021/ja036972z. 
  • Herrera, Raquel P.; Valentina Sgarzani; Luca Bernardi; Alfredo Ricci. Catalytic Enantioselective Friedel-Crafts Alkylation of Indoles with Nitroalkenes by Using a Simple Thiourea Organocatalyst. Angewandte Chemie International Edition. 2005, 44 (40): 6576–6579. ISSN 1433-7851. PMID 16172992. doi:10.1002/anie.200500227. 
  • Wang, Jian; Hao Li; Xinhong Yu; Liansuo Zu; Wei Wang. Chiral Binaphthyl-Derived Amine-Thiourea Organocatalyst-Promoted Asymmetric Morita−Baylis−Hillman Reaction. Organic Letters. 2005, 7 (19): 4293–4296. ISSN 1523-7060. PMID 16146410. doi:10.1021/ol051822+. 
  • Vakulya, Benedek; Szilárd Varga; Antal Csámpai; Tibor Soós. Highly Enantioselective Conjugate Addition of Nitromethane to Chalcones Using Bifunctional Cinchona Organocatalysts. Organic Letters. 2005, 7 (10): 1967–1969. ISSN 1523-7060. PMID 15876031. doi:10.1021/ol050431s. 
  • McCooey, Séamus H.; Stephen J. Connon. Urea- and Thiourea-Substituted Cinchona Alkaloid Derivatives as Highly Efficient Bifunctional Organocatalysts for the Asymmetric Addition of Malonate to Nitroalkenes: Inversion of Configuration at C9 Dramatically Improves Catalyst Performance. Angewandte Chemie International Edition. 2005, 44 (39): 6367–6370. ISSN 1433-7851. PMID 16136619. doi:10.1002/anie.200501721. 
  • Cao, Chun-Li; Meng-Chun Ye; Xiu-Li Sun; Yong Tang. Pyrrolidine−Thiourea as a Bifunctional Organocatalyst: Highly Enantioselective Michael Addition of Cyclohexanone to Nitroolefins. Organic Letters. 2006, 8 (14): 2901–2904. ISSN 1523-7060. PMID 16805512. doi:10.1021/ol060481c. 
  • Yamaoka, Yousuke; Hideto Miyabe; Yoshiji Takemoto. Catalytic Enantioselective Petasis-Type Reaction of Quinolines Catalyzed by a Newly Designed Thiourea Catalyst. Journal of the American Chemical Society. 2007, 129 (21): 6686–6687. ISSN 0002-7863. PMID 17488015. doi:10.1021/ja071470x. 
  • Liu, Kun; Han-Feng Cui; Jing Nie; Ke-Yan Dong; Xiao-Juan Li; Jun-An Ma. Highly Enantioselective Michael Addition of Aromatic Ketones to Nitroolefins Promoted by Chiral Bifunctional Primary Amine-thiourea Catalysts Based on Saccharides. Organic Letters. 2007, 9 (5): 923–925. ISSN 1523-7060. PMID 17288432. doi:10.1021/ol0701666. 

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geb.uni-giessen.de

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