In situ formed bifunctional primary amine-imine catalyst for asymmetric aldol reactions of α-keto esters.
暂无分享,去创建一个
Yixiang Cheng | Chengjian Zhu | Wei Li | A. Lin | Ling Fang | Xi Zhu | Aijun Lin
[1] K. Jørgensen,et al. Organocatalysis--after the gold rush. , 2009, Chemical Society reviews.
[2] M. Raj,et al. Highly Enantioselective Organocatalytic syn‐ and anti‐Aldol Reactions in Aqueous Medium , 2009 .
[3] Yixin Lu,et al. Asymmetric catalysis with chiral primary amine-based organocatalysts. , 2009, Chemical communications.
[4] Yi Pan,et al. Catalytic Asymmetric Ring-Opening Reaction of meso-Epoxides with Aryl Selenols and Thiols Catalyzed by a Heterobimetallic Gallium-Titanium-Salen Complex , 2009 .
[5] Arjan W. Kleij,et al. Nonsymmetrical Salen Ligands and Their Complexes: Synthesis and Applications , 2009 .
[6] Bao-Lei Zheng,et al. Facile preparation of optically pure diamines and their applications in asymmetric aldol reactions , 2008 .
[7] Jianxiong Jiang,et al. Homogeneous silicone modified primary amine-Brønsted acid salt catalyzed aldol reaction: unexpected synergistic effect of polysiloxane with remarkable improvement of efficiency and stereoselectivity , 2008 .
[8] Jianxiong Jiang,et al. Noyori’s Ts-DPEN ligand: an efficient bifunctional primary amine-based organocatalyst in enantio- and diastereoselective Michael addition of 1,3-dicarbonyl indane compounds to nitroolefins , 2008 .
[9] W. Duan,et al. A Novel Bifunctional Sulfonamide Primary Amine‐Catalyzed Enantioselective Conjugate Addition of Ketones to Nitroolefins , 2008 .
[10] Z. Shao,et al. Highly Diastereo‐ and Enantioselective Direct Aldol Reactions Promoted by Water‐Compatible Organocatalysts Bearing Central and Axial Chiral Elements , 2008 .
[11] B. List,et al. Enantiogruppen‐differenzierende intramolekulare Aldolisierung durch Katalyse mit einem primären Amin , 2008 .
[12] Jian Zhou,et al. Primary-amine-catalyzed enantioselective intramolecular aldolizations. , 2008, Angewandte Chemie.
[13] D. MacMillan,et al. The advent and development of organocatalysis , 2008, Nature.
[14] Changwei Hu,et al. Highly Efficient Amine Organocatalysts Based on Bispidine for the Asymmetric Michael Addition of Ketones to Nitroolefins , 2008 .
[15] T. Clark,et al. Evidence for an enol mechanism in a highly enantioselective Mannich-type reaction catalyzed by primary amine-thiourea. , 2008, Angewandte Chemie.
[16] A. Dondoni,et al. Asymmetrische Organokatalyse: Eintritt in die Reifezeit† , 2008 .
[17] Alessandro Massi,et al. Asymmetric organocatalysis: from infancy to adolescence. , 2008, Angewandte Chemie.
[18] Xinhong Yu,et al. Organocatalysis: asymmetric cascade reactions catalysed by chiral secondary amines. , 2008, Organic & biomolecular chemistry.
[19] Changwei Hu,et al. Asymmetric direct aldol reaction of functionalized ketones catalyzed by amine organocatalysts based on bispidine. , 2008, Journal of the American Chemical Society.
[20] Arjan W. Kleij,et al. Materialanwendungen für Salenstrukturen , 2008 .
[21] Arjan W. Kleij,et al. Material applications for salen frameworks. , 2008, Angewandte Chemie.
[22] Yi Wang,et al. Enantioselective Diels-Alder reaction of simple alpha,beta-unsaturated ketones with a cinchona alkaloid catalyst. , 2008, Journal of the American Chemical Society.
[23] S. Mukherjee,et al. Asymmetric enamine catalysis. , 2007, Chemical reviews.
[24] Xiaoming Feng,et al. Asymmetric Direct Aldol Reaction of α‐Keto Esters and Acetone Catalyzed by Bifunctional Organocatalysts , 2007 .
[25] L. Gong,et al. Asymmetric Organocatalytic Direct Aldol Reactions of Ketones with α-Keto Acids and Their Application to the Synthesis of 2-Hydroxy-γ-butyrolactones , 2007 .
[26] Wei Chen,et al. Enantioselective 1,3-dipolar cycloaddition of cyclic enones catalyzed by multifunctional primary amines: beneficial effects of hydrogen bonding. , 2007, Angewandte Chemie.
[27] L. Gong,et al. Design of organocatalysts for asymmetric direct syn-aldol reactions. , 2007, Organic letters.
[28] K. Jiang,et al. Organocatalytic and Highly Enantioselective Direct α-Amination of Aromatic Ketones , 2007 .
[29] Yan Liu,et al. Asymmetric Diels-Alder reactions of 2-pyrones with a bifunctional organic catalyst. , 2007, Journal of the American Chemical Society.
[30] Han-Ming Shen,et al. Highly Efficient Threonine-Derived Organocatalysts for Direct Asymmetric Aldol Reactions in Water , 2007 .
[31] Long Zhang,et al. A simple primary-tertiary diamine-Brønsted acid catalyst for asymmetric direct aldol reactions of linear aliphatic ketones. , 2007, Journal of the American Chemical Society.
[32] D. Enders,et al. Asymmetrische organokatalytische Dominoreaktionen , 2007 .
[33] D. Enders,et al. Asymmetric organocatalytic domino reactions. , 2007, Angewandte Chemie.
[34] Jun‐An Ma,et al. Highly enantioselective Michael addition of aromatic ketones to nitroolefins promoted by chiral bifunctional primary amine-thiourea catalysts based on saccharides. , 2007, Organic letters.
[35] S. Connon,et al. Readily accessible 9-epi-amino cinchona alkaloid derivatives promote efficient, highly enantioselective additions of aldehydes and ketones to nitroolefins. , 2007, Organic letters.
[36] F. Tanaka,et al. Direct catalytic asymmetric synthesis of anti-1,2-amino alcohols and syn-1,2-diols through organocatalytic anti-Mannich and syn-aldol reactions. , 2007, Journal of the American Chemical Society.
[37] Tommaso Marcelli,et al. Cupreine und Cupreidine: eine außergewöhnliche Klasse von bifunktionalen Cinchona‐Organokatalysatoren , 2006 .
[38] J. V. van Maarseveen,et al. Cupreines and cupreidines: an emerging class of bifunctional cinchona organocatalysts. , 2006, Angewandte Chemie.
[39] A. Sakakura,et al. Enantioselective Diels–Alder Reaction of α‐Acyloxyacroleins Catalyzed by Chiral 1,1′‐Binaphthyl‐2,2′‐diammonium Salts , 2006 .
[40] E. Jacobsen,et al. A Chiral Primary Amine Thiourea Catalyst for the Highly Enantioselective Direct Conjugate Addition of α,α‐Disubstituted Aldehydes to Nitroalkenes , 2006 .
[41] H. García,et al. Chiral salen complexes: an overview to recoverable and reusable homogeneous and heterogeneous catalysts. , 2006, Chemical reviews.
[42] N. Tang,et al. Enantioselective epoxidation of olefins catalyzed by chiral dimeric and partially water-soluble monomeric salen-Mn(III) complexes in the presence of novel co-catalysts , 2006 .
[43] A. Córdova,et al. Direct asymmetric intermolecular aldol reactions catalyzed by amino acids and small peptides. , 2006, Chemistry.
[44] E. Jacobsen,et al. Highly enantioselective direct conjugate addition of ketones to nitroalkenes promoted by a chiral primary amine-thiourea catalyst. , 2006, Journal of the American Chemical Society.
[45] S. Tsogoeva,et al. Chiral thiourea-based bifunctional organocatalysts in the asymmetric nitro-michael addition : A joint experimental-theoretical study , 2006 .
[46] S. Tsogoeva,et al. Highly enantioselective addition of ketones to nitroolefins catalyzed by new thiourea-amine bifunctional organocatalysts. , 2006, Chemical communications.
[47] X. Cui,et al. Design of highly enantioselective organocatalysts based on molecular recognition. , 2006, Organic letters.
[48] Yijun Huang,et al. Highly enantioselective Biginelli reaction using a new chiral ytterbium catalyst: asymmetric synthesis of dihydropyrimidines. , 2006, Journal of the American Chemical Society.
[49] F. Himo,et al. The origin of stereoselectivity in primary amino acid catalyzed intermolecular aldol reactions. , 2005, Angewandte Chemie.
[50] T. Kano,et al. A practical synthesis of (S)-2-cyclohexyl-2-phenylglycolic acid via organocatalytic asymmetric construction of a tetrasubstituted carbon center. , 2005, Organic letters.
[51] Wei Wang,et al. Direct, pyrrolidine sulfonamide promoted enantioselective aldol reactions of α,α-dialkyl aldehydes: synthesis of quaternary carbon-containing β-hydroxy carbonyl compounds , 2005 .
[52] S. Tsogoeva,et al. (S)-Histidine-based dipeptides as organic catalysts for direct asymmetric aldol reactions , 2005 .
[53] Yijun Huang,et al. Enantioselective ring-opening reaction of meso-epoxides with ArSeH catalyzed by heterometallic Ti-Ga-Salen system. , 2005, Organic letters.
[54] A. M. Daly,et al. Unsymmetrical chiral salen Schiff base ligands. Synthesis and use in metal-based asymmetric epoxidation reactions , 2005 .
[55] Q. Xia,et al. Advances in homogeneous and heterogeneous catalytic asymmetric epoxidation. , 2005, Chemical reviews.
[56] Yi Pan,et al. Efficient asymmetric oxidation of sulfides and kinetic resolution of sulfoxides catalyzed by a vanadium-salan system. , 2004, The Journal of organic chemistry.
[57] Peter I. Dalko,et al. Im Goldenen Zeitalter der Organokatalyse , 2004 .
[58] P. Dalko,et al. In the golden age of organocatalysis. , 2004, Angewandte Chemie.
[59] F. Tanaka,et al. Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-alder reactions. , 2004, Accounts of chemical research.
[60] B. List. Enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents. , 2004, Accounts of chemical research.
[61] F. Tanaka,et al. Synthesis of beta-hydroxyaldehydes with stereogenic quaternary carbon centers by direct organocatalytic asymmetric aldol reactions. , 2004, Angewandte Chemie.
[62] N. Kumaragurubaran,et al. Direct catalytic asymmetric aldol reactions of aldehydes. , 2002, Chemical communications.
[63] C. Barbas,et al. Amino acid catalyzed direct asymmetric aldol reactions: a bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions. , 2001, Journal of the American Chemical Society.
[64] S. Nguyen,et al. Unsymmetrical salen-type ligands: high yield synthesis of salen-type Schiff bases containing two different benzaldehyde moieties , 2001 .
[65] D. MacMillan,et al. New Strategies for Organic Catalysis: The First Highly Enantioselective Organocatalytic Diels−Alder Reaction , 2000 .
[66] Richard A. Lerner,et al. Proline-Catalyzed Direct Asymmetric Aldol Reactions , 2000 .
[67] A. M. Daly,et al. Unsymmetrical salen ligands: Synthesis and use in chromium mediated asymmetric epoxidation , 1999 .
[68] E. Mintz,et al. Novel unsymmetric chiral Schiff bases possessing two different donor moieties: unique tetradentate ligands from combination of salicylaldehyde and acetylacetone units , 1998 .
[69] X. Bu,et al. Unsymmetric chiral salen Schiff bases: A new chiral ligand pool from bis-schiff bases containing two different salicylaldehyde units , 1998 .
[70] Scott R. Wilson,et al. Enantioselective Epoxidation of Unfunctionalized Olefins Catalyzed by (salen)Manganese Complexes , 1990 .