Catalysts are key to some of the most important reactions on the planet; a world without the Haber process or catalysts to crack crude oil is difficult to imagine. Not to mention the enzymatic reactions that are crucial to all life on earth.
Organocatalysts are an important class of catalyst and consist of carbon-based molecules often functionalised with oxygen, sulfur, nitrogen or phosphorus. They have shown promise in a range of reactions including hydrogenation, Diels-Alder, Michael and Mannich reactions, and are of particular interest in asymmetric reactions.
To help keep you up-to-date with the latest in cutting-edge organocatalytic research we have made the following articles free to access until 9th July. After reading all these there will be little you won’t know about the exciting world of organocatalysis!
Organocatalytic asymmetric transfer hydrogenation of imines
Johannes G. de Vries and Nataša Mršić
Catal. Sci. Technol., 2011, 1, 727-735
Asymmetric organocatalytic formation of protected and unprotected tetroses under potentially prebiotic conditions
Laurence Burroughs, Paul A. Clarke, Henrietta Forintos, James A. R. Gilks, Christopher J. Hayes, Matthew E. Vale, William Wade and Myriam Zbytniewski
Org. Biomol. Chem., 2012, 10, 1565-1570
Recent efforts directed to the development of more sustainable asymmetric organocatalysis
José G. Hernández and Eusebio Juaristi
Chem. Commun., 2012, 48, 5396-5409
Organocatalysis with dendrimers
Anne-Marie Caminade, Armelle Ouali, Michel Keller and Jean-Pierre Majoral
Chem. Soc. Rev., 2012, 41, 4113-4125
Highly efficient direct large-scale stoichiometric aldol reactions catalyzed by a new diamine salt in the presence of water
Jing Huang, Guodong Chen, Xiangkai Fu, Chao Li, Chuanlong Wu and Qiang Miao
Catal. Sci. Technol., 2012, 2, 547-553
Design, synthesis, and application of tartaric acid derived N-spiro quaternary ammonium salts as chiral phase-transfer catalysts
Mario Waser, Katharina Gratzer, Richard Herchl and Norbert Müller
Org. Biomol. Chem., 2012, 10, 251-254
Catalytic, enantio- and diastereoselective synthesis of γ-butyrolactones incorporating quaternary stereocentres
Francesco Manoni, Claudio Cornaggia, James Murray, Sean Tallon and Stephen J. Connon
Chem. Commun., 2012, Advance Article, DOI=10.1039/C2CC32147E
Efficient organocatalysts derived from simple chiral acyclic amino acids in asymmetric catalysis
Zhuo Chai and Gang Zhao
Catal. Sci. Technol., 2012, 2, 29-41
Squaramide-catalyzed enantioselective Michael addition of malononitrile to chalcones
Wen Yang, Yang Jia and Da-Ming Du
Org. Biomol. Chem., 2012, 10, 332-338
Chiral proton catalysis of secondary nitroalkane additions to azomethine: synthesis of a potent GlyT1 inhibitor
Tyler A. Davis, Michael W. Danneman and Jeffrey N. Johnston
Chem. Commun., 2012, 48, 5578-5580
Organocatalytic umpolung: N-heterocyclic carbenes and beyond
Xavier Bugaut and Frank Glorius
Chem. Soc. Rev., 2012, 41, 3511-3522
Asymmetric organocatalytic reactions by bifunctional amine-thioureas
Woon-Yew Siau and Jian Wang
Catal. Sci. Technol., 2011, 1, 1298-1310
Organocatalytic asymmetric tandem condensation–intramolecular rearrangement–protonation: an approach to optically active α-amino thioester derivatives
Francesca Capitta, Angelo Frongia, Pier Paolo Piras, Patrizia Pitzanti and Francesco Secci
Org. Biomol. Chem., 2012, 10, 490-494
Direct asymmetric Mannich reaction of phthalides: facile access to chiral substituted isoquinolines and isoquinolinones
Jie Luo, Haifei Wang, Fangrui Zhong, Jacek Kwiatkowski, Li-Wen Xu and Yixin Lu
Chem. Commun., 2012, 48, 4707-4709
Synthesis, characterization and ethylene oligomerization behaviour of 8-(1-aryliminoethylidene)quinaldinylnickel dihalides
Shengju Song, Tianpengfei Xiao, Tongling Liang, Fosong Wang, Carl Redshaw and Wen-Hua Sun
Catal. Sci. Technol., 2011, 1, 69-75
Asymmetric organocascades involving the formation of two C–heteroatom bonds from two distinct heteroatoms
Damien Bonne, Thierry Constantieux, Yoann Coquerel and Jean Rodriguez
Org. Biomol. Chem., 2012, 10, 3969-3973
Poly(methylhydrosiloxane)-supported chiral imidazolinones: new versatile, highly efficient and recyclable organocatalysts for stereoselective Diels–Alder cycloaddition reactions
Stefania Guizzetti, Maurizio Benaglia and Jay S. Siegel
Chem. Commun., 2012, 48, 3188-3190
Recent advances in asymmetric catalysis with cinchona alkaloid-based primary amines
Lin Jiang and Ying-Chun Chen
Catal. Sci. Technol., 2011, 1, 354-365
Enantioselective synthesis of fluorene derivatives by chiral N-triflyl phosphoramide catalyzed double Friedel–Crafts alkylation reaction
Shou-Guo Wang, Long Han, Mi Zeng, Feng-Lai Sun, Wei Zhang and Shu-Li You
Org. Biomol. Chem., 2012, 10, 3202-3209
Dioxindole in asymmetric catalytic synthesis: direct access to 3-substituted 3-hydroxy-2-oxindoles via 1,4-additions to nitroalkenes
Michele Retini, Giulia Bergonzini and Paolo Melchiorre
Chem. Commun., 2012, 48, 3336-3338
Organocatalytic synthesis of carbohydrates
Jacek Mlynarski and Bartosz Gut
Chem. Soc. Rev., 2012, 41, 587-596
Tetraethylammonium 2-(N-hydroxycarbamoyl)benzoate: a powerful bifunctional metal-free catalyst for efficient and rapid cyanosilylation of carbonyl compounds under mild conditions
Mohammad G. Dekamin, Zahra Karimi and Mehdi Farahmand
Catal. Sci. Technol., 2012, Advance Article, DOI=10.1039/C2CY20037F
Synthesis of symmetric anhydrides using visible light-mediated photoredox catalysis
Marlena D. Konieczynska, Chunhui Dai and Corey R. J. Stephenson
Org. Biomol. Chem., 2012, 10, 4509-4511
Catalytic enantioselective synthesis of β-trifluoromethyl pyrrolines
Hiroyuki Kawai, Takashi Kitayama, Etsuko Tokunaga, Takashi Matsumoto, Hiroyasu Sato, Motoo Shiro and Norio Shibata
Chem. Commun., 2012, 48, 4067-4069
Recent advances in cooperative ion pairing in asymmetric organocatalysis
Jean-François Brière, Sylvain Oudeyer, Vincent Dalla and Vincent Levacher
Chem. Soc. Rev., 2012, 41, 1696-1707
If you’ve enjoyed these articles make sure to take a look at the joint ChemComm-OBC web themed issue, highlighting recent cutting-edge achievements in the field of organocatalysis.
Also check out ChemComm, Catalysis Science & Technology, Chem Soc Rev and OBC for more high impact research and reviews!
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