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61. Full Text Nickel‐Catalyzed α‐Allylation of Aldehydes and Tandem Aldol Condensation/Allylation Reaction with Allylic Alcohols
by Bernhard, Yann and Thomson, Brodie and Ferey, Vincent and Sauthier, Mathieu
Angewandte Chemie (International ed.), ISSN 1433-7851, 06/2017, Volume 56, Issue 26, pp. 7460 - 7464
nickel | allylations | aldehydes | homogeneous catalysis | allylic alcohols
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62. Full Text Recent Advances on Asymmetric Nitroso Aldol Reaction
by Merino, Pedro and Tejero, Tomás and Delso, Ignacio and Matute, Rosa
Synthesis (Stuttgart), ISSN 0039-7881, 03/2016, Volume 48, Issue 5, pp. 653 - 676
short review | aminoxylation | hydroxyamination | α-amino carbonyls | α-hydroxy carbonyls | chiral Lewis acids | asymmetric nitroso aldol | organocatalysts | Physical Sciences | Chemistry | Chemistry, Organic | Science & Technology
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63. Full Text Lewis base catalysis of the Mukaiyama directed aldol reaction: 40years of inspiration and advances
by Beutner, Gregory L and Denmark, Scott E
Angewandte Chemie (International ed.), ISSN 1433-7851, 08/2013, Volume 52, Issue 35, pp. 9086 - 9096
enantioselectivity | silanes | aldol reaction | diastereoselectivity | Lewis bases | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Catalysis
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64. Full Text Stereoselective Synthesis of 3,5‐Dihydroxypyrrolidin‐2‐ones Through a Photoinduced Multicomponent Reaction Followed by Dimerization
by Bergamaschi, Enrico and Capurro, Pietro and Lambruschini, Chiara and Riva, Renata and Basso, Andrea
European journal of organic chemistry, ISSN 1434-193X, 09/2019, Volume 2019, Issue 34, pp. 5992 - 5997
Heterocycles | Multicomponent reactions | Enols | Aldol reactions | Photochemistry | Stereoselectivity | Aldehydes | Natural products | Dimerization
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65. Full Text New understandings of ethanol oxidation reaction mechanism on Pd/C and Pd2Ru/C catalysts in alkaline direct ethanol fuel cells
by Guo, Junsong and Chen, Rongrong and Zhu, Fu-Chun and Sun, Shi-Gang and Villullas, Hebe M
Applied catalysis. B, Environmental, ISSN 0926-3373, 05/2018, Volume 224, pp. 602 - 611
Catalyst deactivation | Alkaline direct alcohol fuel cells | Ethanol electro-oxidation | Engineering | Physical Sciences | Engineering, Chemical | Chemistry | Engineering, Environmental | Technology | Chemistry, Physical | Science & Technology
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66. Full Text Core–shell silica magnetic microspheres supported proline as a recyclable organocatalyst for the asymmetric aldol reaction
by Yang, Honglei and Li, Shuwen and Wang, Xiaoyu and Zhang, Fengwei and Zhong, Xing and Dong, Zhengping and Ma, Jiantai
Journal of molecular catalysis. A, Chemical, ISSN 1381-1169, 11/2012, Volume 363-364, pp. 404 - 410
Supported proline | Recyclable organocatalyst | Silica magnetic nanoparticles | Asymmetric aldol reaction | Physical Sciences | Chemistry | Chemistry, Physical | Science & Technology | Physical and chemical studies. Granulometry. Electrokinetic phenomena | Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry | Exact sciences and technology | General and physical chemistry | Catalysis | Colloidal state and disperse state | Proline | Silica
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67. Full Text Carbene‐Catalyzed Enantioselective Aldol Reaction: Post‐Aldol Stereochemistry Control and Formation of Quaternary Stereogenic Centers
by Yang, Xing and Majhi, Pankaj Kumar and Chai, Huifang and Liu, Bin and Sun, Jun and Liu, Ting and Liu, Yonggui and Zhou, Liejin and Xu, Jun and Liu, Jiawei and Wang, Dongdong and Zhao, Yanli and Jin, Zhichao and Chi, Yonggui Robin
Angewandte Chemie (International ed.), ISSN 1433-7851, 01/2021, Volume 60, Issue 1, pp. 159 - 165
N-heterocyclic carbene | aldol reaction | asymmetric catalysis | acylation | dynamic kinetic resolution | Thermodynamics | Catalysis | Carbonates | Acylation | Stereochemistry | Catalysts | Enantiomers | Aldehydes | Carbon | Substrates | Index Medicus
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68. Full Text Solvent-free asymmetric aldol reaction organocatalyzed by (S)-proline-containing thiodipeptides under ball-milling conditions
by Hernández, José G and García-López, Víctor and Juaristi, Eusebio
Tetrahedron, ISSN 0040-4020, 01/2012, Volume 68, Issue 1, pp. 92 - 97
Green chemistry | Ball-milling | Thiodipeptides | Organocatalysis | Isatin derivatives | Asymmetric aldol reaction | Chemical engineering | Exact sciences and technology | Alicyclic compounds, terpenoids, prostaglandins, steroids | Alicyclic compounds | Grinding | Preparations and properties | Organic chemistry | Chemistry | Solid-solid systems | Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry | Heterocyclic compounds | Heterocyclic compounds with only one n hetero atom and condensed derivatives | Applied sciences | General and physical chemistry | Catalysis | Catalysts: preparations and properties | Aldehydes | Amides | Proline | Pyridine | Cyclohexanone | Milling (machining) | Asymmetry | Tetrahedrons | Segments | Derivatives | Acetone
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69. Full Text Novel prolinamide–ureas as organocatalysts for the asymmetric aldol reaction
by Revelou, Panagiota and Kokotos, Christoforos G and Moutevelis-Minakakis, Panagiota
Tetrahedron, ISSN 0040-4020, 10/2012, Volume 68, Issue 42, pp. 8732 - 8738
Ureas | Aldol reaction | Prolinamides | Asymmetric synthesis | Organocatalysis | Chemistry | General and physical chemistry | Catalysis | Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry | Catalysts: preparations and properties | Exact sciences and technology | Diamines | Ketones | Asymmetry | Tetrahedrons | Transformations | Aldehydes
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70. Full Text Catalytic, Enantioselective Vinylogous Mukaiyama Aldol Reaction of Furan‐Based Dienoxy Silanes: A Chemodivergent Approach to γ‐Valerolactone Flavan‐3‐ol Metabolites and δ‐Lactone Analogues
by Curti, Claudio and Brindani, Nicoletta and Battistini, Lucia and Sartori, Andrea and Pelosi, Giorgio and Mena, Pedro and Brighenti, Furio and Zanardi, Franca and Del Rio, Daniele
Advanced synthesis & catalysis, ISSN 1615-4150, 12/2015, Volume 357, Issue 18, pp. 4082 - 4092
deoxygenation | lactones | asymmetric synthesis | vinylogous aldol reaction | flavan‐3‐ol metabolites | ring expansion | flavan-3-ol metabolites | Silanes | Biological effects | Synthesis | Asymmetry | Metabolites | Precursors | Catalysis | Aldehydes
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71. Full Text Probing the gas-phase structure of charge-tagged intermediates of a proline catalyzed aldol reaction-vibrational spectroscopy distinguishes oxazolidinone from enamine species
by Willms, J. Alexander and Vidic, Jandro and Barthelmes, Janosch and Steinmetz, Vincent and Bredow, Thomas and Maître, Philippe and Engeser, Marianne
Physical chemistry chemical physics : PCCP, ISSN 1463-9076, 2019, Volume 21, Issue 5, pp. 2578 - 2586
Physical Sciences | Chemistry | Physics, Atomic, Molecular & Chemical | Chemistry, Physical | Physics | Science & Technology | Gases - chemistry | Vibration | Models, Chemical | Malonates - chemistry | Density Functional Theory | Catalysis | Mass Spectrometry - methods | Aldehydes - chemistry | Chemistry Techniques, Synthetic - methods | Oxazolidinones - chemistry | Proline - chemistry | Index Medicus | Analytical chemistry | Organic chemistry | Chemical Sciences
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72. Full Text l-proline modulated zirconium metal organic frameworks: Simple chiral catalysts for the aldol addition reaction
by Feng, Xiao and Jena, Himanshu Sekhar and Leus, Karen and Wang, Guangbo and Ouwehand, Judith and Van Der Voort, Pascal
Journal of catalysis, ISSN 0021-9517, 09/2018, Volume 365, pp. 36 - 42
Defect | Aldol reaction | Zr-MOFs | l-proline | Modulation synthesis | L-proline | Engineering | Physical Sciences | Engineering, Chemical | Chemistry | Technology | Chemistry, Physical | Science & Technology | Proline | Zirconium | Catalysis | Catalysts | Leaching
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