Search

Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
---|---|---|---|---|
2,6-diphenyl-4-benzylidenecyclohexa-2,5-dienone![]() ![]() |
E Param.: -11.87 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2009, , 3203-3211 10.1002/ejoc.200900299 | |
2-(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dien-1-ylidene)acetonitrile![]() ![]() |
E Param.: -11.88 | ![]() ![]() ![]() | Chem. Eur. J. 2025, , EarlyView 10.1002/chem.202501224 | |
jul(S)BBS![]() ![]() |
E Param.: -11.89 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
N-(trifluoromethyl)thio)phthalimide![]() ![]() |
E Param.: -11.92 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | |
ethyl 2-(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dien-1-ylidene)acetate![]() ![]() |
E Param.: -12.01 | ![]() ![]() ![]() | Chem. Eur. J. 2025, , EarlyView 10.1002/chem.202501224 | |
o-chloranil (C-Cl)![]() ![]() |
E Param.: -12.02 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b | |
2-cinnamoyl-1-(2,6-dimethoxyphenyl)-3-methyl-1H-imidazol-3-ium![]() ![]() |
DMSO | E Param.: -12.02 | ![]() ![]() ![]() | Top. Catal. 2018, 61, 585-590 10.1007/s11244-018-0[...] |
ethenesulfonyl fluoride (ESF)![]() ![]() |
DMSO | E Param.: -12.09 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2016, 55, 12664-12667 10.1002/anie.201601875 |
p-chloranil (C=O)![]() ![]() |
E Param.: -12.13 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b | |
ani(Ph)2QM![]() ![]() |
E Param.: -12.18 | ![]() ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | |
di-tert-butyl azodicarboxylate![]() ![]() |
MeCN | E Param.: -12.23 | ![]() ![]() ![]() | Chem. Eur. J. 2010, 16, 11670-11677 10.1002/chem.201001598 |
2,5-dichloroquinone (C-H)![]() ![]() |
E Param.: -12.28 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b | |
2,4-dinitrothiophene![]() ![]() |
E Param.: -12.33 | ![]() ![]() ![]() | J. Org. Chem. 2005, 70, 6242-6253 10.1021/jo0505526 | |
4-nitro-<i>trans-beta</i>-nitrostyrene![]() ![]() |
E Param.: -12.37 | ![]() ![]() ![]() | J. Org. Chem. 2011, 76, 9370-9378 10.1021/jo201678u | |
N-(trifluoromethyl)thio)succinimide![]() ![]() |
E Param.: -12.56 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | |
4-cyano-<i>trans-beta</i>-nitrostyrene![]() ![]() |
E Param.: -12.61 | ![]() ![]() ![]() | J. Org. Chem. 2011, 76, 9370-9378 10.1021/jo201678u | |
dmaBBS![]() ![]() |
E Param.: -12.76 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
p-(dimethylamino)benzylidene Meldrum's acid![]() ![]() |
E Param.: -12.76 | ![]() ![]() ![]() | J. Org. Chem. 2008, 73, 2738-2745 10.1021/jo702590s | |
Umemoto II (triflate)![]() ![]() |
E Param.: -12.80 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 | |
benzaldehyde (in DMSO)![]() ![]() |
DMSO | E Param.: -12.90 | ![]() | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
News
- 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).