Dual stereocontrol over the Henry reaction using a light- and heat-triggered organocatalyst.
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[1] S. Luis,et al. New advances in dual stereocontrol for asymmetric reactions. , 2013, Chemical Society reviews.
[2] N. Kumagai,et al. Catalytic chemical transformations with conformationally dynamic catalytic systems , 2013 .
[3] J. Canary,et al. A redox-reconfigurable, ambidextrous asymmetric catalyst. , 2012, Journal of the American Chemical Society.
[4] T. Soós,et al. Active conformation in amine-thiourea bifunctional organocatalysis preformed by catalyst aggregation. , 2012, Chemistry.
[5] M. Suginome,et al. Catalytic asymmetric synthesis using chirality-switchable helical polymer as a chiral ligand , 2012 .
[6] K. Nakayama,et al. An achiral-acid-induced switch in the enantioselectivity of a chiral cis-diamine-based organocatalyst for asymmetric aldol and Mannich reactions. , 2012, Angewandte Chemie.
[7] A. Urakawa,et al. Diastereodivergent asymmetric sulfa-Michael additions of α-branched enones using a single chiral organic catalyst. , 2011, Journal of the American Chemical Society.
[8] Yolanda Alvarez-Casao,et al. Organocatalytic Enantioselective Henry Reactions , 2011, Symmetry.
[9] S. Matsunaga,et al. Stereodivergent direct catalytic asymmetric Mannich-type reactions of α-isothiocyanato ester with ketimines. , 2011, Angewandte Chemie.
[10] Ben L Feringa,et al. Dynamic Control of Chiral Space in a Catalytic Asymmetric Reaction Using a Molecular Motor , 2011, Science.
[11] S. Connon,et al. A new class of urea-substituted cinchona alkaloids promote highly enantioselective nitroaldol reactions of trifluoromethylketones. , 2011, Organic letters.
[12] Shinji Tanaka,et al. Solvent-dependent enantiodivergent Mannich-type reaction: utilizing a conformationally flexible guanidine/bisthiourea organocatalyst. , 2010, Angewandte Chemie.
[13] S. Hecht,et al. Artificial light-gated catalyst systems. , 2010, Angewandte Chemie.
[14] M. Suginome,et al. High-molecular-weight polyquinoxaline-based helically chiral phosphine (PQXphos) as chirality-switchable, reusable, and highly enantioselective monodentate ligand in catalytic asymmetric hydrosilylation of styrenes. , 2010, Journal of the American Chemical Society.
[15] A. Armstrong,et al. Unusual reversal of enantioselectivity in the proline-mediated alpha-amination of aldehydes induced by tertiary amine additives. , 2010, Journal of the American Chemical Society.
[16] M. Bartók. Unexpected inversions in asymmetric reactions: reactions with chiral metal complexes, chiral organocatalysts, and heterogeneous chiral catalysts. , 2010, Chemical reviews.
[17] C. Wolf,et al. Asymmetric copper(I)-catalyzed Henry reaction with an aminoindanol-derived bisoxazolidine ligand. , 2009, Organic letters.
[18] T. Naito,et al. Metal-controlled Reversal of Enantioselectivity in Catalyzed Asymmetric Ring-opening Reactions of meso-Epoxides in Water , 2009 .
[19] P. Schreiner,et al. (Thio)urea organocatalysis--what can be learnt from anion recognition? , 2009, Chemical Society reviews.
[20] N. Kumagai,et al. Linking structural dynamics and functional diversity in asymmetric catalysis. , 2009, Journal of the American Chemical Society.
[21] W. Wulff,et al. Enantioselective organocatalytic direct Michael addition of nitroalkanes to nitroalkenes promoted by a unique bifunctional DMAP-thiourea. , 2008, Journal of the American Chemical Society.
[22] M. Bandini,et al. Enantioselective organocatalyzed Henry reaction with fluoromethyl ketones. , 2008, Chemical communications.
[23] J. M. Saa,et al. Direct, catalytic enantioselective nitroaldol (Henry) reaction of trifluoromethyl ketones: an asymmetric entry to alpha-trifluoromethyl-substituted quaternary carbons. , 2007, Organic letters.
[24] C. Palomo,et al. Recent Advances in the Catalytic Asymmetric Nitroaldol (Henry) Reaction , 2007 .
[25] Ben L Feringa,et al. The art of building small: from molecular switches to molecular motors. , 2007, The Journal of organic chemistry.
[26] Mark S. Taylor,et al. Asymmetric catalysis by chiral hydrogen-bond donors. , 2006, Angewandte Chemie.
[27] Y. Takemoto,et al. Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogen-bonding donors. , 2005, Organic & biomolecular chemistry.
[28] J. N. Johnston,et al. Chiral proton catalysis: a catalytic enantioselective direct aza-Henry reaction. , 2004, Journal of the American Chemical Society.
[29] P. Schreiner. Metal-free organocatalysis through explicit hydrogen bonding interactions. , 2003, Chemical Society reviews.
[30] M. Franzini,et al. Toggling enantioselective catalysis--a promising paradigm in the development of more efficient and versatile enantioselective synthetic methodologies. , 2003, Chemical Society reviews.
[31] Y. H. Kim. Dual enantioselective control in asymmetric synthesis. , 2001, Accounts of chemical research.
[32] M. Sibi,et al. Reversal of Stereochemistry in Enantioselective Transformations. Can They Be Planned or Are They Just Accidental , 2001 .
[33] N. Harada,et al. Light-driven monodirectional molecular rotor , 2022 .