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

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27 | 28 | 29 | 30 | 31 | 32 | 33 | 34 | 35Found 1683 molecules, page 31 of 85
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Name Solvent Reactivity
Parameters 		Classification Reference
(title or year)
cinnamaldehyde (in DMSO)
C9H8O*
 DMSO-J. Am. Chem. Soc. 2011, 133, 8240-8251
10.1021/ja200820m
p-nitro-cinnamaldehyde (in DMSO)
C9H7NO3*
 DMSO-J. Am. Chem. Soc. 2011, 133, 8240-8251
10.1021/ja200820m
acetate (in MeCN)
*
 MeCN

N  Param.: 16.90

sN Param.: 0.75		***J. Am. Chem. Soc. 2008, 130, 3012-3022
10.1021/ja0765464
acetate (in 90A10W)
*
 aq acetone

N  Param.: 12.71

sN Param.: 0.68		***J. Am. Chem. Soc. 2008, 130, 3012-3022
10.1021/ja0765464
acetate (in 80A20W)
*
 aq acetone

N  Param.: 12.50

sN Param.: 0.60		**J. Am. Chem. Soc. 2008, 130, 3012-3022
10.1021/ja0765464
benzoate (in MeCN)
*
 MeCN

N  Param.: 16.82

sN Param.: 0.70		***J. Am. Chem. Soc. 2008, 130, 3012-3022
10.1021/ja0765464
benzoate (in 90AN10W)
*
 aq MeCN

N  Param.: 11.30

sN Param.: 0.72		**J. Am. Chem. Soc. 2008, 130, 3012-3022
10.1021/ja0765464
p-nitrobenzoate (in MeCN)
*
 MeCN

N  Param.: 15.30

sN Param.: 0.76		***J. Am. Chem. Soc. 2008, 130, 3012-3022
10.1021/ja0765464
p-nitrobenzoate (in acetone)
*
 acetone

N  Param.: 18.74

sN Param.: 0.68		***J. Am. Chem. Soc. 2008, 130, 3012-3022
10.1021/ja0765464
3,5-dinitrobenzoate (in MeCN)
*
 MeCN

N  Param.: 14.90

sN Param.: 0.71		**J. Am. Chem. Soc. 2008, 130, 3012-3022
10.1021/ja0765464
3,5-dinitrobenzoate (in acetone)
*
 acetone

N  Param.: 18.80

sN Param.: 0.62		**J. Am. Chem. Soc. 2008, 130, 3012-3022
10.1021/ja0765464
methyl carbonate (in MeCN)
*
 MeCN

N  Param.: 16.03

sN Param.: 0.64		***Eur. J. Org. Chem. 2010, , 4205-4210
10.1002/ejoc.201000414
3,5,6,7-tetrahydro-2H-imidazo[2,1-b][1,3]thiazine
*
 dichloromethane

N  Param.: 13.00

sN Param.: 0.83		***J. Org. Chem. 2011, 76, 5104-5112
10.1021/jo200803x
2,3,5,6-tetrahydroimidazo[2,1-b]thiazole
*
 dichloromethane

N  Param.: 12.98

sN Param.: 0.81		***J. Org. Chem. 2011, 76, 5104-5112
10.1021/jo200803x
2,3-dihydrobenzo[d]imidazo[2,1-b]thiazole
*
 dichloromethane

N  Param.: 13.42

sN Param.: 0.73		***J. Org. Chem. 2011, 76, 5104-5112
10.1021/jo200803x
2,3,4,6,7,8-hexahydropyrimido[2,1-b][1,3]thiazine
*
 dichloromethane

N  Param.: 14.10

sN Param.: 0.82		***J. Org. Chem. 2011, 76, 5104-5112
10.1021/jo200803x
THTP (3,5,6,7-tetrahydro-2H-thiazolo[3,2-a]pyrimidine)
*
 dichloromethane

N  Param.: 14.45

sN Param.: 0.78		***J. Org. Chem. 2011, 76, 5104-5112
10.1021/jo200803x
DHPB (3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine)
*
 dichloromethane

N  Param.: 13.86

sN Param.: 0.78		***J. Org. Chem. 2011, 76, 5104-5112
10.1021/jo200803x
(S)-2-phenyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine
*
 dichloromethane

N  Param.: 13.45

sN Param.: 0.72		***J. Org. Chem. 2011, 76, 5104-5112
10.1021/jo200803x
(2S,3S)-3-isopropyl-2-phenyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine
*
 dichloromethane

N  Param.: 14.96

sN Param.: 0.64		***J. Org. Chem. 2011, 76, 5104-5112
10.1021/jo200803x

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).