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Mayr's Database of Reactivity Parameters

• Advanced Search
• Nucleophiles (1310)
  • 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)(0)
    • 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 (327)
    • 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. (56)
    • Other N-centered nucleophiles (10)
  • S- and Se-Nucleophiles (33)
  • P-Nucleophiles (18)
• Electrophiles (373)
  • C-Electrophiles (348)
    • 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 (135)
      • Acyl azolium ions (6)
      • Baylis-Hillman adducts (7)
      • Benzylidenemalonates (9)
      • Bissulfonyl ethylenes (7)
      • 1,2-Diaza-1,3-dienes (6)
      • Quinone Methides (37)
      • 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(0)
    • Azodicarboxylates (4)
  • Cl-Electrophiles (chlorinating reagents) (3)
  • F-Electrophiles (fluorinating reagents) (5)
  • S-Electrophiles (thiolating reagents) (9)

• Info

  • About the database
  • Search Function
  • Further reading
  • Reactivity Scales Posters
  • Contact
  • Acknowledgement

Search

Search In 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)₂ — — — C=C(OR)(OSi) — — Enamines, Enamides, and Ynamides — — Diazo Compounds and Hydrazones — — Isonitriles — — Metal-&pi;-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-&pi;-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-&#946;</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

N/E-Parameter Range

Keyword

Exact search

15 | 16 | 17 | 18 | 19 | 20 | 21 | 22 | 23« Back Forward »Found 1683 molecules, page 19 of 85

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Name	Solvent	Reactivity Parameters	Classification	Reference (title or year)
1-aminopropan-2-ol (in DMSO)	DMSO	N  Param.: 15.47 sN Param.: 0.65		J. Am. Chem. Soc. 2009, 131, 11392-11401 10.1021/ja903207b
1-benzyl-2-phenyl-4,5-dihydro-1H-imidazole (in CH2Cl2)	dichloromethane	N  Param.: 13.11 sN Param.: 0.83		Eur. J. Org. Chem. 2013, , 3369-3377 10.1002/ejoc.201300213
1-butoxy-1-(t-butyl-dimethylsiloxy)ethene	dichloromethane	N  Param.: 10.32 sN Param.: 0.79		Eur. J. Org. Chem. 2004, , 2791-2796 10.1002/ejoc.200400134
1-butoxy-1-(trimethylsiloxy)ethene	dichloromethane	N  Param.: 10.21 sN Param.: 0.82		Eur. J. Org. Chem. 2004, , 2791-2796 10.1002/ejoc.200400134
1-ethinylcyclohexenyl-Co2(CO)6	dichloromethane	N  Param.: -0.44 sN Param.: 1.06		J. Am. Chem. Soc. 2001, 123, 9500-9512 10.1021/ja010890y
1-ethoxy-2-methyl-1,3-dioxobutan-2-ide (in DMSO)	DMSO	N  Param.: 19.58 sN Param.: 0.73		Eur. J. Org. Chem. 2015, , 7594-7601 10.1002/ejoc.201501107
1-ethoxy-3-(4-nitrophenyl)-1,3-dioxopropan-2-ide (in DMSO)	DMSO	N  Param.: 16.26 sN Param.: 0.83		J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147
1-hexene	dichloromethane	N  Param.: -2.77 sN Param.: 1.41		J. Am. Chem. Soc. 2012, 134, 13902-13911 10.1021/ja306522b
1-mesityl-3-methyl-5-methylene-2,4,6-triphenyl-2,5-dihydropyridin-1-ium-2-ide (in THF)	THF	N  Param.: 26.16 sN Param.: 0.52		Angew. Chem. Int. Ed. 2024, , e202318283 10.1002/anie.202318283
1-methoxy-2-methyl-1-(trimethylsiloxy)propene	dichloromethane	N  Param.: 9.00 sN Param.: 0.98		J. Am. Chem. Soc. 2001, 123, 9500-9512 10.1021/ja010890y
1-methoxy-2-methyl-1-(trimethylsiloxy)propene (in MeCN)	MeCN	N  Param.: 9.11 sN Param.: 0.88		J. Am. Chem. Soc. 2013, 135, 6579-6587 10.1021/ja401106x
1-methyl uracil anion (in DMSO)	DMSO	N  Param.: 16.36 sN Param.: 0.69		Chem. Eur. J. 2012, 18, 127-137 10.1002/chem.201102411
1-methyl uracil anion (in water)	water	N  Param.: 8.54 sN Param.: 0.77		Chem. Eur. J. 2012, 18, 127-137 10.1002/chem.201102411
1-methyl-2,3,4,6,7,8-hexahydro-1H-pyrimido[1,2-a]pyrimidine (MeTBD)	dichloromethane	N  Param.: 14.43 sN Param.: 0.81		ChemCatChem 2012, 4, 993-999 10.1002/cctc.201200143
1-methyl-2-methylene-3-phenyl-1,2-dihydropyridine (in DMSO)	DMSO	N  Param.: 19.41 sN Param.: 0.61		Eur. J. Org. Chem. 2024, 27, e202400373 10.1002/ejoc.202400373
1-methyl-2-phenylpyrrolidine (in CH2Cl2)	dichloromethane	N  Param.: 16.80 sN Param.: 0.49		J. Phys. Org. Chem. 2016, 29, 759-767 10.1002/poc.3580
1-methyl-2-phenylpyrrolidine (in MeCN)	MeCN	N  Param.: 15.70 sN Param.: 0.54		J. Phys. Org. Chem. 2016, 29, 759-767 10.1002/poc.3580
1-methyl-3-((julolidin-9-yl)methylene)-3H-indol-1-ium ion		E Param.: -7.79		J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298
1-methyl-3-(4-methylbenzylidene)-3H-indol-1-ium ion		E Param.: -2.19		J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298
1-methyl-4-(N-morpholino)tetrahydropyridine	dichloromethane	N  Param.: 12.03 sN Param.: 0.80		Chem. Eur. J. 2003, 9, 2209-2218 10.1002/chem.200204666

News

• 1
• 2
• 3
• 4
• 5
• 6
• 7
• 8

• 01/30/25:
  Sesamol-derived ortho-quinone methides (o-QM) have been added (ChemEurJ 2024, e202403785 & OBC 2025, 23, 827-834)
• 05/22/24:
  Lactone enolates have been added (JOC 2024, 89, 6915-6928).
• 11/13/24:
  2-Methylene-1,2-dihydropyridines (2-pyNHOs) have been added (EurJOC 2024, 27, e202400373).
• 05/21/24:
  Mesoionic pyridinium-derived N-heterocyclic olefins (py-mNHOs) have been added (Angew. Chem. Int. Ed. 2024, 63, e202318283).
• 10/19/23:
  Enamines derived from 4-(alkylthio)-3-imidazolines and aldehydes have been added (ChemEurJ 2023, doi: 10.1002/chem.202302764).
• 09/28/23:
  Mesoionic N-heterocyclic olefins (mNHOs) have been added (Angew. Chem. Int. Ed. 2023, 62, e202309790).
• 07/05/23:
  S-Cyanomethylated imidazolidine-4-thione-derived enamines have been added (ChemComm 2023, 59, 8091).
• 03/16/23:
  Cyclic alpha-diazo carbonyl compounds added (EurJOC 2023, 26, e202300005)
• 01/30/23:
  NADH and NADPH reactivities (in water, pH 7) determined by Mayer and Moran have been added (OBC 2022, 21, 85-88).
• 09/20/22:
  Alkenyl boronate nucleophilicity by Liu, Ready and co-workers has been added (JACS 2022, 144, 16118).
• 01/30/23:
  Electrophilicities of diazo compounds in azo couplings (ChemEurJ 2022, 28, e202201376)
• 01/30/23:
  Diazocyclopentadiene added (Synthesis 2023, 55, 354-358)
• 01/30/23:
  Electrophilic indoles added (ChemCommun 2021, 57, 10071-10074)
• 04/13/21:
  Cyclic Michael acceptors added (Chem. Sci. 2021, 12, 4850-4865)
• 05/21/21:
  Thiophenolates (in DMSO) added (JOC 2021, 86, 5965-5972)
• 05/06/20:
  Heteroallenes added (JACS 2020, 142, 8383-8402).
• 01/27/20:
  Pyrrolidines and Imidazolidinones added (JACS 2020, 142, 1526-1547).
• 05/06/20:
  GSH reactivity added (Angew. Chem. Int. Ed. 2019, 58, 17704-17708)
• 01/30/23:
  Phenolates added (JOC 2019, 84, 8837-8858)
• 04/24/18:
  Ketones added (JACS 2018, 140, 5500).
• 11/03/17:
  Allyl-boron nucleophiles added (JACS 2017, 139, 15324)
• 04/23/18:
  Peroxide anions added (Angew. Chem. Int. Ed. 2017, 56, 13279).
• 04/23/18:
  Michael acceptors added (JACS 2017, 139, 13318).
• 06/16/17:
  Nucleophilicities of VNS reagents (JOC 2017, 82, 1011).