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Organometallics
- Ni, Pd, Pt, Co, Rh, Ir, Fe, Ru, and Os Compounds
(Groups 10-8) 
- Mn..., Cr..., V..., Ti..., Sc..., Lanthanide, and Actinide Compounds
(Groups 7-3) 
- Zn, Cd, Hg, Cu, Ag, and Au Compounds
(Groups 12 and 11) 
- Silicon Compounds and As, Sb, Bi Compounds
(Group 15) 
- Ge, Sn, and Pb Compounds
(Group 14) 
- Boron Compounds
- Al, Ga, In, Tl, and Be...Ba Compounds
(Groups 13 and 2) 
- Li, Na, K, Rb, and Cs Compounds
(Group 1) 
Functional Groups
- X—C≡X, X=C=X, X2C=X, CX4 Compounds
- Nitriles, Isocyanides, and Derivatives
- Acid Halides, Carboxylic Acids, Esters, Anhydrides, Peroxy Acids
- Amides and Derivatives, Peptides, Lactams
- Thio-, Seleno-, and Tellurocarboxylic Acids, Imidic Acids, Ortho Acids
- Ketenes
- Ketene Acetals, Yne—X Compounds
- Aldehydes
- Ketones
- Heteroatom Analogues of Aldehydes and Ketones
- Quinones and Heteroatom Analogues
- Acetals: Hal/X and O/O, S, Se, Te
- Acetals: O/N, S/S, S/N, and N/N and Higher Heteroatom Analogues
- Arene—X (X = Hal, O, S, Se, Te, N, P)
- X—Ene—X (X = F, Cl, Br, I, O, S, Se, Te, N, P),
Ene—Hal , and Ene—O Compounds
- Ene—X Compounds (X = S, Se, Te, N, P)
- Fluoroalkanes
- Chloro-, Bromo-, and Iodoalkanes
- Alcohols
- Alkyl Ethers
- Peroxides
- Alkylsulfur, -selenium, and -tellurium Compounds
- Alkylamines, Ammonium Salts, Amine N-Oxides, Haloamines, Hydroxylamines and Sulfur Analogues, Hydrazines
- Nitro, Nitroso, Azo, Azoxy, Diazonium Compounds, Azides, Triazenes, Tetrazenes
- Organophosphorus Compounds
Trends & Innovation
- Advances in Organoboron Chemistry towards Organic Synthesis
- Asymmetric Organocatalysis
- Base Metal Catalysis
- Biocatalysis in Organic Synthesis
- C-1 Building Blocks in Organic Synthesis
- Catalytic Oxidation in Organic Synthesis
- Catalytic Reduction in Organic Synthesis
- C–H Activation
- Click Chemistry
- Cross Coupling and Heck-Type Reactions
- Dual Catalysis in Organic Synthesis
- Domino Transformations in Organic Synthesis
- Dynamic Kinetic Resolution (DKR) and Dynamic Kinetic Asymmetric Transformations (DYKAT)
- Electrochemistry in Organic Synthesis
- Flow Chemistry in Organic Synthesis
- Free Radicals in Organic Synthesis
- Metal-Catalyzed Cyclization Reactions
- Multicomponent Reactions
- N-Heterocyclic Carbenes in Catalytic Organic Synthesis
- Photocatalysis in Organic Synthesis
- Stereoselective Synthesis
- Water in Organic Synthesis
Hetarenes
- Small-Ring Heterocycles, Monocyclic Five-Membered Hetarenes with One Heteroatom
- Fused Five-Membered Hetarenes with One Heteroatom
- Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom
- Five-Membered Hetarenes with Two Nitrogen or Phosphorus Atoms
- Five-Membered Hetarenes with Three or More Heteroatoms
- Six-Membered Hetarenes with One Chalcogen
- Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom
- Six-Membered Hetarenes with Two Identical Heteroatoms
- Six-Membered Hetarenes with Two Unlike or More Than Two Heteroatoms, Larger Hetero-Rings
Hydrocarbons
New! Early View
- Cross-Dehydrogenative Coupling: Development and Perspectives
- (Het)Arene/(Het)Arene Cross-Dehydrogenative Coupling for C(sp
2 )— C(sp2 ) Bond Formation - (Het)Arene/Alkene Cross-Dehydrogenative Coupling for C(sp
2 )— C(sp2 ) Bond Formation - Alkene/Alkene Cross-Dehydrogenative Coupling for C(sp
2 )— C(sp2 ) Bond Formation - (Het)Arene/Alkane Cross-Dehydrogenative Coupling for C(sp
2 )— C(sp3 ) Bond Formation - C
— C Bond Formation in Flow Systems Through Cross-Dehydrogenative Coupling - C
— C Bond Formation through Cross-Dehydrogenative Coupling in Natural Product and API Synthesis - C
— O Bond Formation through Cross-Dehydrogenative Coupling gem -Diborylalkanes- Borepins
- Acid Fluorides (Update 2023)
- Base-Metal-Mediated Cross Couplings Using
N -(Acyloxy)phthalimides - Cobalt- and Iron-Catalyzed Hydrosilylation
- Cobalt- and Iron-Catalyzed Hydroboration
- C
— H Functionalization Catalyzed by Cobalt(III)/Cp* and Related Complexes - C
— H Functionalization Catalyzed by Low-Valent Cobalt - Cobalt-Catalyzed Cross-Coupling Reactions
- Iron-Catalyzed C
— H Functionalization - Iron-Catalyzed Cross Coupling of Aryl and Vinyl Electrophiles
- Iron-Based Chiral Lewis Acid Catalysts in Organic Synthesis
- Manganese-, Iron-, and Cobalt-Catalyzed Radical Alkene Hydrofunctionalization
- Manganese-Catalyzed C
— H Functionalization - Chromium-Catalyzed Cross Coupling and C
— H Functionalization - Catalytic Nozaki–Hiyama–Kishi (NHK) Type Reactions
News
SOS Author Spotlight: Elena Villani and Shinsuke Inagi
Bipolar electrochemistryin Science of Synthesis. Bipolar electrochemistry has...
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