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According to log k20°C = sN(N + E)
Currently the database contains the reactivity parameters of 1294 nucleophiles and 355 electrophiles.
News: Cyclic alpha-diazo carbonyl compounds added (EurJOC 2023, 26, e202300005)
Covered nucleophilicity range:
-8.80 ≤ N ≤ 31.92
Covered electrophilicity range:
-29.60 ≤ E ≤ 8.02
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Currently covered molecule classes
- Nucleophiles (1302)
- C-Nucleophiles (572)
- Alkenes (56)
- Mono-enes (44)
- 1,3-Dienes (12)
- Alkyl, Alkenyl and Aryl Boron Compounds (38)
- Alkylating Boron Compounds (10)
- Alkenylating Boron Compounds (1)
- Arylating Boron Compounds (27)
- Alkynes (1)
- Allyl Element Compounds (38)
- Allyl-B (5)
- Allyl-Si (21)
- Allyl-Sn, Ge, Zn or Fe (12)
- Arenes (42)
- Carbocyclic Arenes (6)
- Indoles (18)
- Pyrroles (7)
- Other Heterocyclic Arenes (11)
- Azolium enolates (4)
- Breslow intermediates (11)
- Desoxy-Breslow intermediates (7)
- O-Methylated Breslow intermediates (4)
- Carbanions (155)
- Carbanions in DMSO (117)
- Carbanions in water (17)
- Carbanions in other solvents (21)
- Carbenes (NHCs) (7)
- Enol Ethers (52)
- C=C-OR (4)
- C=C-OSi (35)
- C=C(OR)2 (1)
- C=C(OR)(OSi) (12)
- Enamines, Enamides, and Ynamides (74)
- Diazo Compounds and Hydrazones (22)
- Isonitriles (5)
- Metal-π-Complexes (5)
- Metallocenes (6)
- NHOs (conventional and mesoionic) (19)
- Vinylsilanes (7)
- Ylides (30)
- Iodonium Ylides (4)
- N-Ylides (9)
- P-Ylides (7)
- S-Ylides (10)
- H-Nucleophiles (193)
- H-B hydride donors (23)
- H-C hydride donors (100)
- H-Si hydride donors (39)
- H-Sn and H-Ge hydride donors (5)
- H-P hydride donors (6)
- transition metal hydride donors (20)
- Halide Anions (29)
- O-Nucleophiles (138)
- Alkoxide Anions (11)
- Amide Anions (O reactivity)
- Alcohols and aqueous solvents (57)
- Ethanol-Acetonitrile mixtures (8)
- Methanol-Acetonitrile mixtures (8)
- Other solvents (pure or mixtures) (11)
- Water-Acetonitrile mixtures (8)
- Water-Ethanol mixtures (7)
- Water-HFIP mixtures (8)
- Water-Trifluoroethanol mixtures (7)
- Carboxylates and Carbonates (11)
- Other O-centered nucleophiles (5)
- Peroxy anions (16)
- Phenolate Ions (38)
- N-Nucleophiles (319)
- Aliphatic amines (104)
- Aromatic amines (7)
- Amide anions (N reactivity) (21)
- Amidines and Imines (10)
- Amino acids (20)
- Azoles and Azole Anions (33)
- Guanidines (8)
- Hydrazines, Hydroxylamines etc. (21)
- Imidazolines and related compounds (10)
- Isothioureas (12)
- Nucleobases and Their Subunits (15)
- Pyridines, Quinolines etc. (48)
- Other N-centered nucleophiles (10)
- S- and Se-Nucleophiles (33)
- P-Nucleophiles (18)
- Electrophiles (363)
- C-Electrophiles (338)
- Carbocations (132)
- Diarylcarbenium Ions (33)
- Triarylcarbenium Ions (25)
- Indolyl-stabilized carbocations (12)
- Other conjugated carbocations (23)
- N-substituted carbocations (iminium ions) (31)
- O-substituted carbocations (carboxonium ions) (5)
- S-substituted carbocations (3)
- Cationic Metal-π-Complexes (20)
- Fe-stabilized carbocations (9)
- Co-stabilized carbocations (5)
- Other metal-stabilized carbocations (6)
- Acceptor-Substituted Ethylenes (125)
- Acyl azolium ions (6)
- Baylis-Hillman adducts (7)
- Benzylidenemalonates (9)
- Bissulfonyl ethylenes (7)
- 1,2-Diaza-1,3-dienes (6)
- Quinone Methides (27)
- trans-β-Nitrostyrenes (6)
- Other Michael acceptors (57)
- Arenes (electron-deficient) (16)
- Aldehydes (11)
- Heteroallenes (X=C=Y) (6)
- Imines (5)
- Ketones (10)
- Quinones (10)
- CF3 transfer reagents (3)
- N-Electrophiles (8)
- Diazo compounds (4)
- Diazonium ions
- Azodicarboxylates (4)
- Cl-Electrophiles (chlorinating reagents) (3)
- F-Electrophiles (fluorinating reagents) (5)
- S-Electrophiles (thiolating reagents) (9)