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1. Full Text Electrochemical Arylation Reaction
by Waldvogel, Siegfried R and Lips, Sebastian and Selt, Maximilian and Riehl, Barbara and Kampf, Christopher J
Chemical Reviews, ISSN 0009-2665, 07/2018, Volume 118, Issue 14, pp. 6706 - 6765
Arylated products are found in various fields of chemistry and represent essential entities for many applications. Therefore, the formation of this structural... 
CROSS-COUPLING REACTION | ONE-POT | ELECTROLYTIC SUBSTITUTION-REACTIONS | IN-SITU ELECTROGENERATION | DIRECT ANODIC-OXIDATION | H AMINATION SYNTHESIS | ORGANIC HALIDES | CHEMISTRY, MULTIDISCIPLINARY | NON-NUCLEOPHILIC MEDIA | ARYLBORONIC ACIDS | HIGH-YIELD REACTION
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2. Full Text Recent synthetic developments in a powerful imino Diels–Alder reaction (Povarov reaction): application to the synthesis of N-polyheterocycles and related alkaloids
by Kouznetsov, Vladimir V
Tetrahedron, ISSN 0040-4020, 2009, Volume 65, Issue 14, pp. 2721 - 2750
This review is devoted to the development in Povarov reaction and focuses on new efficient approaches based on this reaction to construct simple substituted... 
Quinoline derivatives | Polyheterocycles | Alkaloids | Intra- and intermolecular imino Diels–Alder reaction | Cycloaddition | Povarov reaction | Intra- and intermolecular imino Diels-Alder reaction | SOLVENT-FREE CONDITIONS | ONE-STEP SYNTHESIS | ONE-POT SYNTHESIS | CHEMISTRY, ORGANIC | SOLID SUPPORT SYNTHESIS | CATALYZED ONE-POT | Diets-Alder reaction | Intra- and intermolecular imino | 3-COMPONENT COUPLING PROTOCOL | ANTICANCER DRUG TAS-103 | ASYMMETRIC TOTAL-SYNTHESIS | HIGHLY DIASTEREOSELECTIVE SYNTHESIS | 4+2 CYCLOADDITION REACTIONS | Furans | Diels-Alder reaction | Chemical synthesis
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3. Full Text Nitro-Mannich Reaction
by Noble, Adam and Anderson, James C
Chemical Reviews, ISSN 0009-2665, 05/2013, Volume 113, Issue 5, pp. 2887 - 2939
AZA-HENRY REACTION | ASYMMETRIC 1,3-DIPOLAR CYCLOADDITION | THIOUREA-GUANIDINE CATALYST | DEHYDROGENATIVE COUPLING REACTIONS | ONE-POT SYNTHESIS | ALPHA-SUBSTITUTED NITROACETATES | SELECTIVE 3+2 CYCLOADDITION | CHIRAL PROTON CATALYSIS | UBER ALIPHATISCHE NITROVERBINDUNGEN | UMSETZUNGEN DES NITROACETONS | CHEMISTRY, MULTIDISCIPLINARY | Peptides - chemistry | Nitro Compounds - chemistry | Nitriles - chemical synthesis | Nitro Compounds - chemical synthesis | Mannich Bases - chemistry | Chemistry Techniques, Synthetic - methods | Mannich Bases - chemical synthesis | Peptides - chemical synthesis | Metals - chemistry | Imines - chemistry | Nitriles - chemistry | Catalysis | Imines - chemical synthesis | Nitrogen compounds | Chemical reactions | Chemical properties | Research | Catalysts
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4. Full Text An Extremely Efficient Three-Component Reaction of Aldehydes/Ketones, Amines, and Phosphites (Kabachnik−Fields Reaction) for the Synthesis of α-Aminophosphonates Catalyzed by Magnesium Perchlorate
by Bhagat, Srikant and Chakraborti, Asit K
The Journal of Organic Chemistry, ISSN 0022-3263, 02/2007, Volume 72, Issue 4, pp. 1263 - 1270
Commercially available magnesium perchlorate is reported as an extremely efficient catalyst for the synthesis of α-aminophosphonates. A three-component... 
LANTHANIDE TRIFLATE | PHOSPHONATES | SOLVENT-FREE CONDITIONS | ONE-POT SYNTHESIS | STATE ANALOG INHIBITORS | CHEMISTRY, ORGANIC | CARBONYL-COMPOUNDS | ACYLATION CATALYST | IONIC LIQUIDS | MICROWAVE-ASSISTED SYNTHESIS | LEUCINE AMINOPEPTIDASE
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5. Full Text Electrocatalysts for hydrogen evolution reaction
by Eftekhari, Ali
International Journal of Hydrogen Energy, ISSN 0360-3199, 04/2017, Volume 42, Issue 16, pp. 11053 - 11077
In addition to the historical importance of water electrolysis, hydrogen evolution reaction (HER) is the heart of various energy storage and conversation... 
Electrocatalysis | Hydrogen evolution reaction | Water splitting | Metallic catalyst | Metal dichalcogenide | Catalyst support | REDUCED GRAPHENE OXIDE | NICKEL PHOSPHIDE NANOPARTICLES | ELECTROCHEMISTRY | ONE-POT SYNTHESIS | ENERGY & FUELS | MOLYBDENUM-DISULFIDE NANOSHEETS | MOS2 ULTRATHIN NANOSHEETS | HIGH CATALYTIC-ACTIVITY | CHEMISTRY, PHYSICAL | NITROGEN-DOPED-CARBON | ACTIVE EDGE SITES | TRANSITION-METAL CARBIDES | HIGHLY-EFFICIENT | Alternative energy sources | Transition metal compounds | Electrolysis | Catalysts | Hydrogen | Alloys
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6. Full Text From the Feist–Bénary Reaction to Organocatalytic Domino Michael–Alkylation Reactions: Asymmetric Synthesis of 3(2 H)‐Furanones
by Dou, Xiaowei and Han, Xiaoyu and Lu, Yixin
Chemistry – A European Journal, ISSN 0947-6539, 01/2012, Volume 18, Issue 1, pp. 85 - 89
It all adds up! A modified Feist–Bénary reaction employing a domino Michael–alkylation sequence was designed for the enantioselective synthesis of 3(2... 
Feist–Bénary reaction | organocatalysis | furanones | asymmetric synthesis | domino reactions | Feist-Bénary reaction | VINYL SULFONE | Feist-Benary reaction | ONE-POT SYNTHESIS | C BOND FORMATION | 1,3-DICARBONYL COMPOUNDS | AMINE-THIOUREA CATALYST | CHEMISTRY, MULTIDISCIPLINARY | BIFUNCTIONAL ORGANOCATALYSTS | SELECTIVE MANNICH REACTIONS | TETRONIC ACIDS | INTRAMOLECULAR CYCLIZATION | ENANTIOSELECTIVE CONJUGATE ADDITION | Combinatorial Chemistry Techniques | Furans - chemistry | Stereoisomerism | Molecular Structure | Catalysis | Furans - chemical synthesis | Alkylation
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7. Full Text Towards click chemistry: Multicomponent reactions via combinations of name reactions
by Heravi, Majid M and Zadsirjan, Vahideh and Dehghani, Mahzad and Ahmadi, Tahereh
Tetrahedron, ISSN 0040-4020, 07/2018, Volume 74, Issue 27, pp. 3391 - 3457
In this report, we try to show the importance of incorporation of name reactions in the sequential cascade reaction in which significantly decreasing the... 
Heterocycles | Multicomponent reaction | Ugi reaction | Heck reaction | Aldol reaction | Huisgen reaction | Name reaction | Mannich reaction | Click chemistry | Knoevenagel reaction | Diels-Alder reaction | Michael reaction | Suzuki reaction | DIELS-ALDER REACTIONS | ONE-POT SYNTHESIS | KNOEVENAGEL-MICHAEL REACTION | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | PALLADIUM-CATALYZED VINYLATION | ASYMMETRIC ALDOL REACTIONS | REGIOSELECTIVE SYNTHESIS | MODIFIED POLY(STYRENE-CO-MALEIC ANHYDRIDE) | RECYCLABLE CATALYST | HUISGEN 1,3-DIPOLAR CYCLOADDITION
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8. Full Text Vertex‐Reinforced PtCuCo Ternary Nanoframes as Efficient and Stable Electrocatalysts for the Oxygen Reduction Reaction and the Methanol Oxidation Reaction
by Kwon, Taehyun and Jun, Minki and Kim, Ho Young and Oh, Aram and Park, Jongsik and Baik, Hionsuck and Joo, Sang Hoon and Lee, Kwangyeol
Advanced Functional Materials, ISSN 1616-301X, 03/2018, Volume 28, Issue 13, pp. 1706440 - n/a
Noble metal binary alloy nanoframes have emerged as a new class of fuel cell electrocatalysts because of their intrinsic high catalytic surface area and... 
platinum | ternary alloys | fuel cell electrocatalysts | nanoframes | stability | PHYSICS, CONDENSED MATTER | PHYSICS, APPLIED | SHELL | ONE-POT SYNTHESIS | MATERIALS SCIENCE, MULTIDISCIPLINARY | NANOCRYSTALS | CHEMISTRY, PHYSICAL | SHAPE-CONTROLLED SYNTHESIS | NANOSCIENCE & NANOTECHNOLOGY | PT-NI | PHASE SEGREGATION | CHEMISTRY, MULTIDISCIPLINARY | NANOPARTICLES | SURFACE | Oxidation-reduction reaction | Catalysis | Catalysts | Fuel cells | Alloys | Methanol | Structural stability | Electrocatalysts | Catalytic activity | Binary systems (materials) | Cobalt | Chemical reduction | Binary alloys | Platinum | Oxidation | Noble metals | Copper
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9. Full Text Reaction mechanism of nucleoside 2 '-deoxyribosyltransferases: free-energy landscape supports an oxocarbenium ion as the reaction intermediate
by del Arco, J and Perona, A and Gonzalez, L and Fernandez-Lucas, J and Gago, F and Sanchez-Murcia, PA
ORGANIC & BIOMOLECULAR CHEMISTRY, ISSN 1477-0520, 09/2019, Volume 17, Issue 34, pp. 7891 - 7899
Insight into the catalytic mechanism of Lactobacillus leichmannii nucleoside 2 '-deoxyribosyltransferase (LlNDT) has been gained by calculating a quantum... 
SITE | MOLECULAR-DYNAMICS | ONE-STEP SYNTHESIS | EXPEDIENT | ONE-POT | IMPLEMENTATION | CHEMISTRY, ORGANIC | BIOCATALYST | BASIS-SETS | GLYCOSYLATION | 2-DEOXYRIBOSYLTRANSFERASE
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10. Full Text Stereocontrolled Domino Reactions
by Pellissier, Hélène
Chemical Reviews, ISSN 0009-2665, 01/2013, Volume 113, Issue 1, pp. 442 - 524
AZA-MICHAEL REACTION | MULTICOMPONENT REACTIONS | COMPLEX-CATALYZED SYNTHESIS | ONE-POT SYNTHESIS | 3-COMPONENT REACTION | ALPHA-AMINO-ACIDS | ENANTIOSELECTIVE TOTAL-SYNTHESIS | ASYMMETRIC TOTAL-SYNTHESIS | HIGHLY STEREOSELECTIVE-SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | CONJUGATE ADDITION | Organic Chemicals - chemical synthesis | Molecular Structure | Cyclization | Stereoisomerism | Organic Chemicals - chemistry | Metal catalysts | Analysis | Oxidation-reduction reaction | Chemical properties | Ring formation (Chemistry) | Carbenes | Cascade reactions
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11. Full Text Cu-Catalyzed Click Reaction in Carbohydrate Chemistry
by Tiwari, Vinod K and Mishra, Bhuwan B and Mishra, Kunj B and Mishra, Nidhi and Singh, Anoop S and Chen, Xi
Chemical Reviews, ISSN 0009-2665, 03/2016, Volume 116, Issue 5, pp. 3086 - 3240
Cu(I)-catalyzed azide alkyne 1,3-dipolar cycloaddition (CuAAC), popularly known as the "click reaction", serves as the most potent and highly dependable tool... 
AZIDE-ALKYNE CYCLOADDITION | ANTI-HIV DRUG | DECARBOXYLATIVE MANNICH REACTION | LIVING RADICAL POLYMERIZATION | ONE-POT SYNTHESIS | HYDROGENATED CARDANOL CONJUGATE | CRUZI-TRANS-SIALIDASE | NATIVE CHEMICAL LIGATION | CENTERED MULTIVALENT GLYCOCLUSTERS | CHEMISTRY, MULTIDISCIPLINARY | CARBONIC-ANHYDRASE INHIBITORS
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