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Mayr's Database Of Reactivity Parameters: Searches
Mayr's Database of Reactivity Parameters

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Name Solvent Reactivity
Parameters 		Classification Reference
(title or year)
(S)-4-benzyl-1,3-oxazolidin-2-one anion (in DMSO)
*
 DMSO

N  Param.: 22.67

sN Param.: 0.54		***J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
ethyl N-acetylcarbamate anion (in DMSO)
*
 DMSO

N  Param.: 15.99

sN Param.: 0.70		***J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
Me2S=CH-CO2Et (in DMSO)
*
 DMSO

N  Param.: 15.85

sN Param.: 0.61		***Chem. Eur. J. 2010, 16, 8610-8614
10.1002/chem.201001455
Me2S=CH-CN (in DMSO)
*
 DMSO

N  Param.: 16.23

sN Param.: 0.60		***Chem. Eur. J. 2010, 16, 8610-8614
10.1002/chem.201001455
MeSO2-CH-CO2Et (in DMSO)
*
 DMSO

N  Param.: 18.00

sN Param.: 0.66		***Chem. Eur. J. 2010, 16, 8610-8614
10.1002/chem.201001455
MeSO-CH-CO2Et (in DMSO)
*
 DMSO

N  Param.: 20.61

sN Param.: 0.64		***Chem. Eur. J. 2010, 16, 8610-8614
10.1002/chem.201001455
(cyclohexen-1-yl)prolinate (in MeCN)
*
 MeCN

N  Param.: 18.86

sN Param.: 0.70		***Angew. Chem. Int. Ed. 2010, 49, 9526-9529
10.1002/anie.201004344
1-(N-pyrrolidino)cyclohexene (in MeCN)
*
 MeCN

N  Param.: 16.42

sN Param.: 0.70		***Angew. Chem. Int. Ed. 2010, 49, 9526-9529
10.1002/anie.201004344
methyl (cyclohexen-1-yl)prolinate (in MeCN)
*
 MeCN

N  Param.: 14.96

sN Param.: 0.68		***Angew. Chem. Int. Ed. 2010, 49, 9526-9529
10.1002/anie.201004344
2-pyridone anion (in DMSO)
*
 DMSO

N  Param.: 19.91

sN Param.: 0.60		***J. Am. Chem. Soc. 2010, 132, 15380-15389
10.1021/ja106962u
2-pyridone anion (in MeCN)
*
 MeCN

N  Param.: 20.11

sN Param.: 0.57		***J. Am. Chem. Soc. 2010, 132, 15380-15389
10.1021/ja106962u
2-pyridone anion (in water)
*
 water

N  Param.: 12.47

sN Param.: 0.52		***J. Am. Chem. Soc. 2010, 132, 15380-15389
10.1021/ja106962u
4-pyridone anion (in DMSO)
*
 DMSO

N  Param.: 18.97

sN Param.: 0.62		***J. Am. Chem. Soc. 2010, 132, 15380-15389
10.1021/ja106962u
4-pyridone anion (in MeCN)
*
 MeCN

N  Param.: 20.22

sN Param.: 0.49		***J. Am. Chem. Soc. 2010, 132, 15380-15389
10.1021/ja106962u
4-pyridone anion (in water)
*
 water

N  Param.: 14.76

sN Param.: 0.48		***J. Am. Chem. Soc. 2010, 132, 15380-15389
10.1021/ja106962u
saccharin anion (in MeCN)
*
 MeCN

N  Param.: 10.78

sN Param.: 0.89		***J. Org. Chem. 2010, 75, 5250-5258
10.1021/jo1009883
DMSO (O attack)
*
 DMSO

N  Param.: 11.30

sN Param.: 0.74		***J. Am. Chem. Soc. 2009, 131, 11392-11401
10.1021/ja903207b
(4-Br-C6H4)-(CO)-CH=SMe2 (in DMSO)
*
 DMSO

N  Param.: 13.78

sN Param.: 0.72		***J. Am. Chem. Soc. 2010, 132, 17894-17900
10.1021/ja1084749
(C6H5)-(CO)-CH=SMe2 (in DMSO)
*
 DMSO

N  Param.: 13.95

sN Param.: 0.69		***J. Am. Chem. Soc. 2010, 132, 17894-17900
10.1021/ja1084749
(4-MeO-C6H4)-(CO)-CH=SMe2 (in DMSO)
*
 DMSO

N  Param.: 14.48

sN Param.: 0.71		***J. Am. Chem. Soc. 2010, 132, 17894-17900
10.1021/ja1084749

News

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  • 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).