You are using Science Of Synthesis as a Guest.
Please login or request a trial to access the full content.
Please login or request a trial to access the full content.
Explore Science of Synthesis
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
- Cross-Dehydrogenative Coupling
- 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
News
SOS Author Spotlight: Elena Villani and Shinsuke Inagi
Bipolar electrochemistryin Science of Synthesis. Bipolar electrochemistry has...
Return to Top