Search

Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
---|---|---|---|---|
(E)-3-(4-nitro-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO)![]() ![]() |
DMSO | E Param.: -17.33 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m |
(E)-2,6-di-tert-butyl-4-(3-(4-methoxyphenyl)allylidene)cyclohexa-2,5-dien-1-one![]() ![]() |
DMSO | E Param.: -17.42 | ![]() ![]() ![]() | Org. Lett. 2020, 22, 2182-2186 10.1021/acs.orglett.[...] |
cyclobutanone (in DMSO)![]() ![]() |
DMSO | E Param.: -17.50 | ![]() | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
(E)-3-(4-cyano-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO)![]() ![]() |
DMSO | E Param.: -17.64 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m |
diethyl 4-nitrobenzylidene malonate![]() ![]() |
E Param.: -17.67 | ![]() ![]() ![]() | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | |
carbon disulfide![]() ![]() |
DMSO | E Param.: -17.70 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
diethyl fumarate![]() ![]() |
DMSO | E Param.: -17.79 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2014, , 2956-2963 10.1002/ejoc.201301779 |
jul(t-Bu)2QM![]() ![]() |
E Param.: -17.90 | ![]() ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | |
bh6j![]() ![]() |
E Param.: -17.90 | ![]() ![]() | Chem. Eur. J. 2010, 16, 1365-1371 10.1002/chem.200902487 | |
oxan-4-one (in DMSO)![]() ![]() |
DMSO | E Param.: -17.90 | ![]() | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
hex-3-yn-2-one![]() ![]() |
E Param.: -17.90 | ![]() | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 | |
diethyl 4-cyano-benzylidene malonate![]() ![]() |
E Param.: -18.06 | ![]() ![]() ![]() | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | |
phenyl isothiocyanate![]() ![]() |
DMSO | E Param.: -18.15 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
bh 6k![]() ![]() |
E Param.: -18.20 | ![]() | Chem. Eur. J. 2010, 16, 1365-1371 10.1002/chem.200902487 | |
1,4-dioxaspiro[4.5]decan-8-one (in DMSO)![]() ![]() |
DMSO | E Param.: -18.20 | ![]() | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
dimethyl diazomalonate![]() ![]() |
E Param.: -18.20 | ![]() ![]() ![]() | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | |
(p-nitrophenyl)diazomethane![]() ![]() |
E Param.: -18.30 | ![]() ![]() ![]() | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | |
ethenylsulfonylbenzene (in DMSO)![]() ![]() |
DMSO | E Param.: -18.36 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
1-methylpiperidin-4-one (in DMSO)![]() ![]() |
DMSO | E Param.: -18.40 | ![]() | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
methyl diazoacetate![]() ![]() |
E Param.: -18.50 | ![]() ![]() ![]() | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 |
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).