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Class of compounds
Nucleophiles
— C-Nucleophiles
— — Alkenes
— — — Mono-enes
— — — 1,3-Dienes
— — Alkyl, Alkenyl and Aryl Boron Compounds
— — — Alkylating Boron Compounds
— — — Alkenylating Boron Compounds
— — — Arylating Boron Compounds
— — Alkynes
— — Allyl Element Compounds
— — — Allyl-B
— — — Allyl-Si
— — — Allyl-Sn, Ge, Zn or Fe
— — Arenes
— — — Carbocyclic Arenes
— — — Indoles
— — — Pyrroles
— — — Other Heterocyclic Arenes
— — Azolium enolates
— — Breslow intermediates
— — — Desoxy-Breslow intermediates
— — — O-Methylated Breslow intermediates
— — Carbanions
— — — Carbanions in DMSO
— — — Carbanions in water
— — — Carbanions in other solvents
— — Carbenes (NHCs)
— — Enol Ethers
— — — C=C-OR
— — — C=C-OSi
— — — C=C(OR)<sub>2</sub>
— — — C=C(OR)(OSi)
— — Enamines, Enamides, and Ynamides
— — Diazo Compounds and Hydrazones
— — Isonitriles
— — Metal-π-Complexes
— — Metallocenes
— — NHOs (conventional and mesoionic)
— — Vinylsilanes
— — Ylides
— — — Iodonium Ylides
— — — N-Ylides
— — — P-Ylides
— — — S-Ylides
— H-Nucleophiles
— — H-B hydride donors
— — H-C hydride donors
— — H-Si hydride donors
— — H-Sn and H-Ge hydride donors
— — H-P hydride donors
— — transition metal hydride donors
— Halide Anions
— O-Nucleophiles
— — Alkoxide Anions
— — Amide Anions (O reactivity)
— — Alcohols and aqueous solvents
— — — Ethanol-Acetonitrile mixtures
— — — Methanol-Acetonitrile mixtures
— — — Other solvents (pure or mixtures)
— — — Water-Acetonitrile mixtures
— — — Water-Ethanol mixtures
— — — Water-HFIP mixtures
— — — Water-Trifluoroethanol mixtures
— — Carboxylates and Carbonates
— — Other O-centered nucleophiles
— — Peroxy anions
— — Phenolate Ions
— N-Nucleophiles
— — Aliphatic amines
— — Aromatic amines
— — Amide anions (N reactivity)
— — Amidines and Imines
— — Amino acids
— — Azoles and Azole Anions
— — Guanidines
— — Hydrazines, Hydroxylamines etc.
— — Imidazolines and related compounds
— — Isothioureas
— — Nucleobases and Their Subunits
— — Pyridines, Quinolines etc.
— — Other N-centered nucleophiles
— S- and Se-Nucleophiles
— P-Nucleophiles
Electrophiles
— C-Electrophiles
— — Carbocations
— — — Diarylcarbenium Ions
— — — Triarylcarbenium Ions
— — — Indolyl-stabilized carbocations
— — — Other conjugated carbocations
— — — N-substituted carbocations (iminium ions)
— — — O-substituted carbocations (carboxonium ions)
— — — S-substituted carbocations
— — Cationic Metal-π-Complexes
— — — Fe-stabilized carbocations
— — — Co-stabilized carbocations
— — — Other metal-stabilized carbocations
— — Acceptor-Substituted Ethylenes
— — — Acyl azolium ions
— — — Baylis-Hillman adducts
— — — Benzylidenemalonates
— — — Bissulfonyl ethylenes
— — — 1,2-Diaza-1,3-dienes
— — — Quinone Methides
— — — <i>trans-β</i>-Nitrostyrenes
— — — Other Michael acceptors
— — Arenes (electron-deficient)
— — Aldehydes
— — Heteroallenes (X=C=Y)
— — Imines
— — Ketones
— — Quinones
— — CF3 transfer reagents
— N-Electrophiles
— — Diazo compounds
— — Diazonium ions
— — Azodicarboxylates
— Cl-Electrophiles (chlorinating reagents)
— F-Electrophiles (fluorinating reagents)
— S-Electrophiles (thiolating reagents)
Solvent
Search all solvents
1,2-dichloroethane
acetone
aq acetone
aq MeCN
dichloromethane
dichloromethane/MeCN mix
DMF
DMSO
EtOH
EtOH-MeCN mix
HFIP
iPrOH
iPrOH-MeCN mix
MeCN
MeOH
MeOH-MeCN mix
nPrOH
nPrOH-MeCN mix
TFE
THF
water
water-acetone mix
water-EtOH mix
water-HFIP mix
water-MeCN mix
water-TFE mix